Difference between revisions of "Biocluster Applications"

From Carl R. Woese Institute for Genomic Biology - University of Illinois Urbana-Champaign
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!Description
 
!Description
 
|-
 
|-
|efidb
+
|[https://github.com/shawnzhangyx/PePr PePr]
|ip62<br>ip63<br>ip64<br>ip65<br>ip66<br>ip66_private<br>ip67<br>ip68<br>ip69
+
|1.1.21-IGB-gcc-4.9.4-Python-2.7.13
|
+
|PePr is a ChIP-Seq Peak-calling and Prioritization pipeline that uses a sliding window approach and models read counts across replicates and between groups with a negative binomial distribution.
 
|-
 
|-
|efiest
+
|[http://www.libsdl.org/ SDL2]
|beta<br>beta_private<br>devel<br>devlocal<br>prod<br>prod_private
+
|2.0.4-IGB-gcc-4.9.4
|
+
|SDL: Simple DirectMedia Layer, a cross-platform multimedia library
 
|-
 
|-
|efignt
+
|[https://github.com/lebedov/scikit-cuda scikit-cuda]
|beta<br>beta_private<br>devel<br>devlocal<br>prod<br>prod_private
+
|0.5.1-IGB-gcc-4.9.4-Python-2.7.13
|
+
|scikit-cuda provides Python interfaces to many of the functions in the CUDA device/runtime, CUBLAS, CUFFT, and CUSOLVER libraries distributed as part of NVIDIAs CUDA Programming Toolkit, as well as interfaces to select functions in the free and standard versions of the CULA Dense Toolkit. Both low-level wrapper functions similar to their C counterparts and high-level functions comparable to those in NumPy and Scipy are provided.
 
|-
 
|-
|efishared
+
|[http://www.nasm.us/ NASM]
|beta<br>beta_private<br>devel<br>devlocal<br>prod<br>prod_private
+
|.2.12.02-IGB-gcc-4.9.4<br>2.12.02-IGB-gcc-4.9.4
|
+
|NASM: General-purpose x86 assembler
 
|-
 
|-
|shortbred/beta
+
|[http://www.perl.org/ Perl]
|beta
+
|5.24.1-IGB-gcc-4.9.4<br>5.24.1-IGB-gcc-4.9.4-bare<br>5.26.1-IGB-gcc-4.9.4-unthreaded
|
+
|Larry Wall Practical Extraction and Report Language
 
|-
 
|-
|shortbred/devlocal
+
|[https://github.com/ginolhac/mapDamage mapDamage]
|devlocal
+
|2.0.5-IGB-gcc-4.9.4-Python-2.7.13
|
+
|mapDamage2 is a computational framework written in Python and R, which tracks and quantifies DNA damage patterns among ancient DNA sequencing reads generated by Next-Generation Sequencing platforms.
 
|-
 
|-
|shortbred/diamond
+
|[http://sourceforge.net/projects/libjpeg-turbo/ libjpeg-turbo]
|diamond/beta<br>diamond/devlocal
+
|.1.5.1-IGB-gcc-4.9.4
|
+
|libjpeg-turbo is a fork of the original IJG libjpeg which uses SIMD to accelerate baseline JPEGcompression and decompression. libjpeg is a library that implements JPEG image encoding, decoding and transcoding. - Homepage: http://sourceforge.net/projects/libjpeg-turbo/
 
|-
 
|-
|[http://454.com/products/analysis-software/index.asp 454]
+
|[https://github.com/torognes/vsearch VSEARCH]
|2.8
+
|2.4.3-IGB-gcc-4.9.4
|The GS Data Analysis Software package includes the tools to investigate complex genomic variation in samples including de novo assembly, reference guided alignment and variant calling, and low abundance variant identification and quantification. - Homepage: http://454.com/products/analysis-software/index.asp
+
|VSEARCH stands for vectorized search, as the tool takes advantage of parallelism in the form of SIMD vectorization as well as multiple threads to perform accurate alignments at high speed. - Homepage: https://github.com/torognes/vsearch
 
|-
 
|-
|[http://www.bcgsc.ca/platform/bioinfo/software/abyss ABySS]
+
|[http://hibberdlab.com/transrate/ transrate]
|2.0.2-IGB-gcc-4.9.4
+
|1.0.3
|ABySS is a de novo, parallel, paired-end sequence assembler that is designed for short reads. The single-processor version is useful for assembling genomes up to 100 Mbases in size. The parallel version is implemented using MPI and is capable of assembling larger genomes.
+
|Transrate is software for de-novo transcriptome assembly quality analysis. It examines your assembly in detail and compares it to experimental evidence such as the sequencing reads, reporting quality scores for contigs and assemblies.
 
|-
 
|-
|[https://projects.coin-or.org/ADOL-C ADOL-C]
+
|[https://github.com/taoliu/MACS/ MACS2]
|2.6.3-IGB-gcc-4.9.4
+
|2.1.1.20160309-IGB-gcc-4.9.4-Python-2.7.13
|ADOL-C is an open-source package for the automatic differentiation of C and C++ programs.  
+
|Model Based Analysis for ChIP-Seq data - Homepage: https://github.com/taoliu/MACS/
 
|-
 
|-
|[http://vfsmspineagent.fsm.northwestern.edu/ AGEnt]
+
|[http://subread.sourceforge.net/ Subread]
|0.2.1-IGB-gcc-4.9.4
+
|1.5.2-IGB-gcc-4.9.4
|AGEnt performs in silico subtractive hybridization of core genome sequences, such as those produced by Spine, against a query genomic sequence to identify accessory genomic sequences (AGEs) in the query genome. Sequences are aligned using Nucmer, outputting sequences and sequence characteristics of those regions in the query genome that are not found in the core genome. If gene coordinate information is provided, a list of accessory genes in the query genome will also be output.
+
|High performance read alignment, quantification and mutation discovery - Homepage: http://subread.sourceforge.net/
 
|-
 
|-
|[http://www.antlr2.org/ ANTLR]
+
|[http://software.broadinstitute.org/software/igv/ igv]
|.2.7.7-IGB-gcc-4.9.4
+
|2.4.4-Java-1.8.0_152
|ANTLR, ANother Tool for Language Recognition, (formerly PCCTS) is a language tool that provides a framework for constructing recognizers, compilers, and translators from grammatical descriptions containing Java, C#, C++, or Python actions.
+
|The Integrative Genomics Viewer (IGV) is a high-performance visualization tool for interactive exploration of large, integrated genomic datasets. It supports a wide variety of data types, including array-based and next-generation sequence data, and genomic annotations.
 
|-
 
|-
|[https://github.com/bcgsc/arcs ARCS]
+
|[https://bibiserv2.cebitec.uni-bielefeld.de/rnahybrid RNAhybrid]
|1.0.0-IGB-gcc-4.9.4-Perl-5.24.1
+
|2.1.2-IGB-gcc-4.9.4
|Scaffolding genome sequence assemblies using 10X Genomics GemCode/Chromium data. - Homepage: https://github.com/bcgsc/arcs
+
|RNAhybrid is a tool for finding the minimum free energy hybridization of a long and a short RNA. The hybridization is performed in a kind of domain mode, ie. the short sequence is hybridized to the best fitting part of the long one. The tool is primarily meant as a means for microRNA target prediction.  
 
|-
 
|-
|[https://developer.gnome.org/ATK/stable/ ATK]
+
|[http://www.cbs.dtu.dk/cgi-bin/nph-sw_request?signalp SignalP]
|.2.24.0-IGB-gcc-4.9.4-Python-2.7.13<br>.2.24.0-IGB-gcc-4.9.4-Python-3.6.1
+
|4.1
|ATK provides the set of accessibility interfaces that are implemented by other toolkits and applications. Using the ATK interfaces, accessibility tools have full access to view and control running applications.
+
|Signal peptide and cleavage sites in gram+, gram- and eukaryotic amino acid sequences
 
|-
 
|-
|[https://github.com/MikkelSchubert/adapterremoval AdapterRemoval]
+
|[http://www.graphicsmagick.org/ GraphicsMagick]
|2.1.7-IGB-gcc-4.9.4
+
|1.3.26-IGB-gcc-4.9.4
|This program searches for and removes remnant adapter sequences from High-Throughput Sequencing (HTS) data and (optionally) trims low quality bases from the 3 end of reads following adapter removal.  
+
|GraphicsMagick is the swiss army knife of image processing.
 
|-
 
|-
|[https://github.com/DReichLab/AdmixTools AdmixTools]
+
|[http://dri.freedesktop.org libdrm]
|1.0.1-IGB-gcc-4.9.4
+
|.2.4.76-IGB-gcc-4.9.4
|The ADMIXTOOLS package implements 5 methods described in Patterson et al. (2012) Ancient Admixture in Human History. Details of the methods and algorithm can be found in this paper.
+
|Direct Rendering Manager runtime library.
 
|-
 
|-
|[https://www.continuum.io/anaconda-overview Anaconda2]
+
|[http://korflab.ucdavis.edu/software.html SNAP]
|4.3.1
+
|2013-11-29-IGB-gcc-4.9.4
|Built to complement the rich, open source Python community,the Anaconda platform provides an enterprise-ready data analytics platform that empowers companies to adopt a modern open data science analytics architecture. - Homepage: https://www.continuum.io/anaconda-overview
+
|(Semi-HMM-based Nucleic Acid Parser) gene prediction tool
 
|-
 
|-
|[https://www.continuum.io/anaconda-overview Anaconda3]
+
|[http://www.novocraft.com/ novocraft]
|5.0.1<br>5.1.0
+
|3.08.00
|Built to complement the rich, open source Python community,the Anaconda platform provides an enterprise-ready data analytics platform that empowers companies to adopt a modern open data science analytics architecture.
+
|Powerful tool designed for mapping of short reads onto a reference genome from Illumina, Ion Torrent, and 454 NGS platforms.
 
|-
 
|-
|[https://github.com/mgbellemare/Arcade-Learning-Environment ArcadeLearningEnvironment]
+
|[http://research-pub.gene.com/gmap/ GMAP]
|0.5.1-IGB-gcc-4.9.4-Python-2.7.13
+
|2018-05-30-IGB-gcc-4.9.4
|The Arcade Learning Environment (ALE) -- a platform for AI research. - Homepage: https://github.com/mgbellemare/Arcade-Learning-Environment
+
|A Genomic Mapping and Alignment Program for mRNA and EST Sequences, andGSNAP: Genomic Short-read Nucleotide Alignment Program
 
|-
 
|-
|[http://assemblytics.com/ Assemblytics]
+
|[https://github.com/mitoNGS/MToolBox MToolBox]
|3f570cd-IGB-gcc-4.9.4<br>df5361f-IGB-gcc-4.9.4
+
|1.0-IGB-gcc-4.9.4
|Analyze your assembly by comparing it to a reference genome
+
|MToolBox is a highly automated bioinformatics pipeline to reconstruct and analyze human mitochondrial DNA from high throughput sequencing data. MToolBox includes an updated computational strategy to assemble mitochondrial genomes from Whole Exome and/or Genome Sequencing (PMID: 22669646) and an improved fragment-classify tool (PMID:22139932) for haplogroup assignment, functional and prioritization analysis of mitochondrial variants. MToolBox provides pathogenicity scores, profiles of genome variability and disease-associations for mitochondrial variants. MToolBox provides also a Variant Call Format file (version 4.0) featuring, for the first time, allele-specific heteroplasmy.
 
|-
 
|-
|[http://www.gnu.org/software/autoconf/ Autoconf]
+
|[http://www-inf.enst.fr/~demaille/a2ps/ a2ps]
|.2.69<br>.2.69-IGB-gcc-4.9.4
+
|4.14-IGB-gcc-4.9.4
|Autoconf is an extensible package of M4 macros that produce shell scripts to automatically configure software source code packages. These scripts can adapt the packages to many kinds of UNIX-like systems without manual user intervention. Autoconf creates a configuration script for a package from a template file that lists the operating system features that the package can use, in the form of M4 macro calls. - Homepage: http://www.gnu.org/software/autoconf/
+
|a2ps-4.14: Formats an ascii file for printing on a postscript printer
 
|-
 
|-
|[http://www.gnu.org/software/automake/automake.html Automake]
+
|[http://wasabiapp.org/software/pagan PAGAN]
|.1.15<br>.1.15-IGB-gcc-4.9.4
+
|20150723-IGB-gcc-4.9.4
|Automake: GNU Standards-compliant Makefile generator
+
|PAGAN is a general-purpose method for the alignment of sequence graphs. PAGAN is based on the phylogeny-aware progressive alignment algorithm and uses graphs to describe the uncertainty in the presence of characters at certain sequence positions. However, graphs also allow describing the uncertainty in input sequences and modelling e.g. homopolymer errors in Roche 454 reads, or representing inferred ancestral sequences against which other sequences can then be aligned. PAGAN is still under development and will hopefully evolve to an easy-to-use, general-purpose method for phylogenetic sequence alignment.
 
|-
 
|-
|[http://autotools.io Autotools]
+
|[https://github.com/fidelram/deepTools deepTools]
|.20150215<br>.20150215-IGB-gcc-4.9.4
+
|2.5.3-IGB-gcc-4.9.4-Python-2.7.13<br>3.0.1-IGB-gcc-4.9.4-Python-2.7.13
|This bundle collect the standard GNU build tools: Autoconf, Automake and libtool
+
|deepTools addresses the challenge of handling the large amounts of data that are now routinely generated from DNA sequencing centers. deepTools contains useful modules to process the mapped reads data for multiple quality checks, creating normalized coverage files in standard bedGraph and bigWig file formats, that allow comparison between different files (for example, treatment and control). Finally, using such normalized and standardized files, deepTools can create many publication-ready visualizations to identify enrichments and for functional annotations of the genome.
 
|-
 
|-
|[http://www.htslib.org/ BCFtools]
+
|[http://rnaseq-mats.sourceforge.net/ rMATS]
|1.4-IGB-gcc-4.9.4<br>1.5-IGB-gcc-4.9.4<br>1.7-IGB-gcc-4.9.4
+
|3.2.5-IGB-gcc-4.9.4-Python-2.7.13
|BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF
+
|MATS is a computational tool to detect differential alternative splicing events from RNA-Seq data. The statistical model of MATS calculates the P-value and false discovery rate that the difference in the isoform ratio of a gene between two conditions exceeds a given user-defined threshold. From the RNA-Seq data, MATS can automatically detect and analyze alternative splicing events corresponding to all major types of alternative splicing patterns. MATS handles replicate RNA-Seq data from both paired and unpaired study design.
 
|-
 
|-
|[https://github.com/arq5x/bedtools2 BEDTools]
+
|[https://bitbucket.org/feeldead/gfold GFOLD]
|2.21.0-IGB-gcc-4.9.4<br>2.26.0-IGB-gcc-4.9.4
+
|1.1.4-IGB-gcc-4.9.4
|The BEDTools utilities allow one to address common genomics tasks such as finding feature overlaps and computing coverage. The utilities are largely based on four widely-used file formats: BED, GFF/GTF, VCF, and SAM/BAM. - Homepage: https://github.com/arq5x/bedtools2
+
|GFOLD stands for Generalized FOLD change for ranking differentially expressed genes from RNA-seq data. GFOLD is especially useful when no replicate is available. GFOLD generalizes the fold change by considering the posterior distribution of log fold change, such that each gene is assigned a reliable fold change.
 
|-
 
|-
|[https://github.com/PacificBiosciences/blasr BLASR]
+
|[http://www.gnu.org/software/m4/m4.html M4]
|4.0.0-IGB-gcc-4.9.4
+
|.1.4.17-IGB-gcc-4.9.4<br>.1.4.18<br>.1.4.18-GCCcore-4.9.4<br>.1.4.18-IGB-gcc-4.9.4
|BLASR (Basic Local Alignment with Successive Refinement) rapidly maps  reads to genomes by finding the highest scoring local alignment or set of local alignments  between the read and the genome. Optimized for PacBios extraordinarily long reads and  taking advantage of rich quality values, BLASR maps reads rapidly with high accuracy.  
+
|GNU M4 is an implementation of the traditional Unix macro processor. It is mostly SVR4 compatible  although it has some extensions (for example, handling more than 9 positional parameters to macros). GNU M4 also has built-in functions for including files, running shell commands, doing arithmetic, etc.
 
|-
 
|-
|[http://blast.ncbi.nlm.nih.gov/ BLAST]
+
|[https://github.com/md5sam/Falcon2Fastg Falcon2Fastg]
|2.2.26-Linux_x86_64
+
|0.3.1-IGB-gcc-4.9.4-Python-2.7.13
|Basic Local Alignment Search Tool, or BLAST, is an algorithm for comparing primary biological sequence information, such as the amino-acid sequences of different proteins or the nucleotides of DNA sequences.
+
|This software converts the results of PacBio assembly using FALCON, to a FASTG graph that can be visualized using Bandage.
 
|-
 
|-
|[http://blast.ncbi.nlm.nih.gov/ BLAST+]
+
|[https://github.com/GregoryFaust/samblaster samblaster]
|2.6.0-IGB-gcc-4.9.4<br>2.7.1-IGB-gcc-4.9.4<br>2.8.0-IGB-gcc-4.9.4-alpha
+
|0.1.24-IGB-gcc-4.9.4
|Basic Local Alignment Search Tool, or BLAST, is an algorithm for comparing primary biological sequence information, such as the amino-acid sequences of different proteins or the nucleotides of DNA sequences.
+
|ummary samblaster is a fast and flexible program for marking duplicates in read-id grouped1 paired-end SAM files. It can also optionally output discordant read pairs and/or split read mappings to separate SAM files, and/or unmapped/clipped reads to a separate FASTQ file. When marking duplicates, samblaster will require approximately 20MB of memory per 1M read pairs.
 
|-
 
|-
|[http://genome.ucsc.edu/FAQ/FAQblat.html BLAT]
+
|[http://lowelab.ucsc.edu/snoscan/ snoscan]
|3.5-IGB-gcc-4.9.4
+
|0.9.1-IGB-gcc-4.9.4-Perl-5.24.1<br>0.9.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
|BLAT on DNA is designed to quickly find sequences of 95% and greater similarity of length 25 bases or more.
+
|Search for C/D box methylation guide snoRNA genes in a genomic sequence
 
|-
 
|-
|[https://github.com/BSSeeker/BSseeker2 BS-Seeker]
+
|[https://github.com/lvclark/tagdigger tagdigger]
|2.1.2-IGB-gcc-4.9.4-Python-2.7.13
+
|1.1-IGB-gcc-4.9.4-Python-3.6.1
|BS Seeker 2 is a seamless and versatile pipeline for accurately and fast mapping the bisulfite-treated short reads. - Homepage: https://github.com/BSSeeker/BSseeker2
+
|TagDigger is a program for processing FASTQ files from genotyping-by-sequencing (GBS) or restriction site-associated DNA sequencing (RAD-seq) experiments.  
 
|-
 
|-
|[https://github.com/hellbelly/BS-Snper BS-Snper]
+
|[http://expressionanalysis.github.io/ea-utils/ ea-utils]
|20170222-IGB-gcc-4.9.4-Perl-5.24.1
+
|1.04.807-IGB-gcc-4.9.4
|BS-SNPer is an ultrafast and memory-efficient package, a program for BS-Seq variation detection from alignments in standard BAM/SAM format using approximate Bayesian modeling.
+
|Command-line tools for processing biological sequencing data. Barcode demultiplexing, adapter trimming, etc. Primarily written to support an Illumina based pipeline - but should work with any FASTQs.
 
|-
 
|-
|[http://busco.ezlab.org/ BUSCO]
+
|[http://sco.h-its.org/exelixis/web/software/pear/ PEAR]
|3.0.1-IGB-gcc-4.9.4-Python-2.7.13
+
|0.9.8-IGB-gcc-4.9.4
|BUSCO v3 provides quantitative measures for the assessment of genome assembly, gene set, and transcriptome completeness, based on evolutionarily-informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB v9.
+
|PEAR is an ultrafast, memory-efficient and highly accurate pair-end read merger.  It is fully parallelized and can run with as low as just a few kilobytes of memory. - Homepage: http://sco.h-its.org/exelixis/web/software/pear/
 
|-
 
|-
|[http://bio-bwa.sourceforge.net/ BWA]
+
|[http://hmmer.org/ HMMER]
|0.5.9-IGB-gcc-4.9.4<br>0.6.2-IGB-gcc-4.9.4<br>0.7.15-IGB-gcc-4.9.4<br>0.7.17-IGB-gcc-4.9.4
+
|2.3.2-IGB-gcc-4.9.4<br>3.1b2-IGB-gcc-4.9.4<br>3.2.1-IGB-gcc-4.9.4
|Burrows-Wheeler Aligner (BWA) is an efficient program that aligns relatively short nucleotide sequences against a long reference sequence such as the human genome. - Homepage: http://bio-bwa.sourceforge.net/
+
|HMMER is used for searching sequence databases for homologs of protein sequences, and for making protein sequence alignments. It implements methods using probabilistic models called profile hidden Markov models (profile HMMs).  Compared to BLAST, FASTA, and other sequence alignment and database search tools based on older scoring methodology, HMMER aims to be significantly more accurate and more able to detect remote homologs because of the strength of its underlying mathematical models. In the past, this strength came at significant computational expense, but in the new HMMER3 project, HMMER is now essentially as fast as BLAST.
 
|-
 
|-
|[https://github.com/pezmaster31/bamtools BamTools]
+
|[http://rpy.sourceforge.net/ rpy2]
|2.4.1-IGB-gcc-4.9.4
+
|2.8.6-IGB-gcc-4.9.4-Python-2.7.13-R-3.3.3<br>2.9.0-IGB-gcc-4.9.4-Python-3.6.1-R-3.3.3
|BamTools provides both a programmers API and an end-users toolkit for handling BAM files.
+
|rpy2 is a redesign and rewrite of rpy. It is providing a low-level interface to R from Python, a proposed high-level interface, including wrappers to graphical libraries, as well as R-like structures and functions.  
 
|-
 
|-
|[http://www.bioperl.org/ BioPerl]
+
|[http://www.freedesktop.org/wiki/Software/pkg-config/ pkg-config]
|1.7.1-IGB-gcc-4.9.4-Perl-5.24.1<br>1.7.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
+
|.0.29.2-IGB-gcc-4.9.4
|Bioperl is the product of a community effort to produce Perl code which is useful in biology. Examples include Sequence objects, Alignment objects and database searching objects.
+
|pkg-config is a helper tool used when compiling applications and libraries. It helps you insert the correct compiler options on the command line so an application can use  gcc -o test test.c `pkg-config --libs --cflags glib-2.0` for instance, rather than hard-coding values on where to find glib (or other libraries). - Homepage: http://www.freedesktop.org/wiki/Software/pkg-config/
 
|-
 
|-
|[https://github.com/maasha/biopieces Biopieces]
+
|[http://www.usadellab.org/cms/?page=trimmomatic Trimmomatic]
|2.0-IGB-gcc-4.9.4-Perl-5.24.1
+
|0.36-Java-1.8.0_121<br>0.36-Java-1.8.0_152<br>0.38-Java-1.8.0_152
|Biopieces is a bioinformatic framework of tools easily used and easily created.
+
|Trimmomatic performs a variety of useful trimming tasks for illumina paired-end and single ended data.The selection of trimming steps and their associated parameters are supplied on the command line.  
 
|-
 
|-
|[http://www.biopython.org Biopython]
+
|[http://lame.sourceforge.net/ LAME]
|1.68-IGB-gcc-4.9.4-Python-2.7.13<br>1.68-IGB-gcc-4.9.4-Python-3.6.1
+
|3.99.5-IGB-gcc-4.9.4
|Biopython is a set of freely available tools for biological computation writtenin Python by an international team of developers. It is a distributed collaborative effort todevelop Python libraries and applications which address the needs of current and future work inbioinformatics.  - Homepage: http://www.biopython.org
+
|LAME is a high quality MPEG Audio Layer III (MP3) encoder licensed under the LGPL.
 
|-
 
|-
|[http://www.bioinformatics.babraham.ac.uk/projects/bismark/ Bismark]
+
|[http://flex.sourceforge.net/ flex]
|0.17.0-IGB-gcc-4.9.4-Perl-5.24.1<br>0.18.1-IGB-gcc-4.9.4-Perl-5.24.1
+
|.2.6.3<br>.2.6.3-GCCcore-4.9.4
|A tool to map bisulfite converted sequence reads and determine cytosine methylation states - Homepage: http://www.bioinformatics.babraham.ac.uk/projects/bismark/
+
|Flex (Fast Lexical Analyzer) is a tool for generating scanners. A scanner,  sometimes called a tokenizer, is a program which recognizes lexical patterns in text. - Homepage: http://flex.sourceforge.net/
 
|-
 
|-
|[http://www.gnu.org/software/bison Bison]
+
|[https://www.ebi.ac.uk/interpro/interproscan.html InterProScan]
|.3.0.4<br>.3.0.4-GCCcore-4.9.4
+
|5.27-66.0-IGB-gcc-4.9.4-Java-1.8.0_152<br>5.28-67.0-IGB-gcc-4.9.4-Java-1.8.0_152
|Bison is a general-purpose parser generator that converts an annotated context-free grammarinto a deterministic LR or generalized LR (GLR) parser employing LALR(1) parser tables. - Homepage: http://www.gnu.org/software/bison
+
|InterProScan is the software package that allows sequences (protein and nucleic) to be scanned against InterPros signatures. Signatures are predictive models, provided by several different databases, that make up the InterPro consortium.
 
|-
 
|-
|[http://www.boost.org/ Boost]
+
|[http://deeplearning.net/software/libgpuarray pygpu]
|.1.59.0-IGB-gcc-4.9.4<br>.1.63.0-IGB-gcc-4.9.4<br>.1.63.0-IGB-gcc-4.9.4-Python-2.7.13
+
|0.6.5-IGB-gcc-4.9.4-Python-2.7.13
|Boost provides free peer-reviewed portable C++ source libraries. - Homepage: http://www.boost.org/
+
|Python bindings for libgpuarray - Homepage: http://deeplearning.net/software/libgpuarray
 
|-
 
|-
|[http://bowtie-bio.sourceforge.net/index.shtml Bowtie]
+
|[http://qt.io/ Qt]
|1.2.0-IGB-gcc-4.9.4
+
|4.8.7-IGB-gcc-4.9.4
|Bowtie is an ultrafast, memory-efficient short read aligner.It aligns short DNA sequences (reads) to the human genome. - Homepage: http://bowtie-bio.sourceforge.net/index.shtml
+
|Qt is a comprehensive cross-platform C++ application framework.
 
|-
 
|-
|[http://bowtie-bio.sourceforge.net/bowtie2/index.shtml Bowtie2]
+
|[https://gradle.org Gradle]
|2.1.0-IGB-gcc-4.9.4<br>2.3.1-IGB-gcc-4.9.4<br>2.3.2-IGB-gcc-4.9.4
+
|4.7
|Bowtie 2 is an ultrafast and memory-efficient tool for aligning sequencing reads  to long reference sequences. It is particularly good at aligning reads of about 50 up to 100s or 1,000s  of characters, and particularly good at aligning to relatively long (e.g. mammalian) genomes.  Bowtie 2 indexes the genome with an FM Index to keep its memory footprint small: for the human genome,  its memory footprint is typically around 3.2 GB. Bowtie 2 supports gapped, local, and paired-end alignment modes. - Homepage: http://bowtie-bio.sourceforge.net/bowtie2/index.shtml
+
|Complete Gradle install.From mobile apps to microservices, from small startups to big enterprises,Gradle helps teams build, automate and deliver better software, faster.  
 
|-
 
|-
|[http://bioinform.github.io/breakseq2/ BreakSeq2]
+
|[http://pytorch.org PyTorch]
|2.2-IGB-gcc-4.9.4-Python-2.7.13
+
|0.3.0-IGB-gcc-4.9.4-Python-3.6.1<br>0.4.0-IGB-gcc-4.9.4-Python-3.6.1
|Ultrafast and accurate nucleotide-resolution analysis of structural variants - Homepage: http://bioinform.github.io/breakseq2/
+
|Tensors and Dynamic neural networks in Pythonwith strong GPU acceleration.
 
|-
 
|-
|[http://weizhong-lab.ucsd.edu/cd-hit/ CD-HIT]
+
|[http://hannonlab.cshl.edu/fastx_toolkit/ libgtextutils]
|4.6.6-IGB-gcc-4.9.4
+
|.0.7-IGB-gcc-4.9.4
|CD-HIT is a very widely used program for clustering and comparing protein or nucleotide sequences. - Homepage: http://weizhong-lab.ucsd.edu/cd-hit/
+
|ligtextutils is a dependency of fastx-toolkit and is provided via the same upstream - Homepage: http://hannonlab.cshl.edu/fastx_toolkit/
 +
|-
 +
|[https://github.com/voutcn/megahit MEGAHIT]
 +
|1.1.1-IGB-gcc-4.9.4
 +
|MEGAHIT is a single node assembler for large and complex metagenomics NGS reads, such as soil. It makes use of succinct de Bruijn graph (SdBG) to achieve low memory assembly. - Homepage: https://github.com/voutcn/megahit
 +
|-
 +
|[http://git-scm.com/ git]
 +
|2.9.5-IGB-gcc-4.9.4
 +
|Git is a free and open source distributed version control system designedto handle everything from small to very large projects with speed and efficiency.
 +
|-
 +
|[https://github.com/maasha/biopieces Biopieces]
 +
|2.0-IGB-gcc-4.9.4-Perl-5.24.1
 +
|Biopieces is a bioinformatic framework of tools easily used and easily created.
 
|-
 
|-
|[http://www.cmake.org CMake]
+
|[https://vcftools.github.io VCFtools]
|.3.12.1-IGB-gcc-4.9.4<br>.3.7.2-IGB-gcc-4.9.4
+
|0.1.15-IGB-gcc-4.9.4-Perl-5.24.1
|CMake, the cross-platform, open-source build system. CMake is a family of tools designed to build, test and package software. - Homepage: http://www.cmake.org
+
|The aim of VCFtools is to provide  easily accessible methods for working with complex  genetic variation data in the form of VCF files. - Homepage: https://vcftools.github.io
 
|-
 
|-
 
|[https://developer.nvidia.com/cuda-toolkit CUDA]
 
|[https://developer.nvidia.com/cuda-toolkit CUDA]
Line 189: Line 201:
 
|CUDA (formerly Compute Unified Device Architecture) is a parallel computing platform and programming model created by NVIDIA and implemented by the graphics processing units (GPUs) that they produce. CUDA gives developers access to the virtual instruction set and memory of the parallel computational elements in CUDA GPUs. - Homepage: https://developer.nvidia.com/cuda-toolkit
 
|CUDA (formerly Compute Unified Device Architecture) is a parallel computing platform and programming model created by NVIDIA and implemented by the graphics processing units (GPUs) that they produce. CUDA gives developers access to the virtual instruction set and memory of the parallel computational elements in CUDA GPUs. - Homepage: https://developer.nvidia.com/cuda-toolkit
 
|-
 
|-
|[http://cunit.sourceforge.net/ CUnit]
+
|[http://meme-suite.org/ MEME]
|2.1-3-IGB-gcc-4.9.4
+
|4.12.0-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13<br>5.0.1-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
|CUnit is a lightweight system for writing, administering, and running unit tests in C. It provides C programmers a basic testing functionality with a flexible variety of user interfaces.
+
|The MEME Suite allows you to: * discover motifs using MEME, DREME (DNA only) or  GLAM2 on groups of related DNA or protein sequences, * search sequence databases with motifs using MAST, FIMO, MCAST or GLAM2SCAN, * compare a motif to all motifs in a database of motifs, * associate  motifs with Gene Ontology terms via their putative target genes, and * analyse motif enrichment  using SpaMo or CentriMo.
 
|-
 
|-
|[https://github.com/marbl/canu Canu]
+
|[https://databank.illinois.edu/ IllinoisDataBank]
|1.4-IGB-gcc-4.9.4-Perl-5.24.1<br>1.5-IGB-gcc-4.9.4-Perl-5.24.1<br>1.6-IGB-gcc-4.9.4-Perl-5.24.1<br>1.7-IGB-gcc-4.9.4-Perl-5.24.1<br>1.7.1-IGB-gcc-4.9.4-Perl-5.24.1
+
|1.0-IGB-gcc-4.9.4-Python-2.7.13
|Canu is a fork of the Celera Assembler, designed for high-noise single-molecule sequencing (such as the PacBio RS II or Oxford Nanopore MinION).
+
|The Illinois Data Bank is a public access repository for publishing research data from the University of Illinois at Urbana-Champaign - Homepage: https://databank.illinois.edu/
 
|-
 
|-
|[http://ecogenomics.github.io/CheckM CheckM]
+
|[http://genome.cse.ucsc.edu kentUtils]
|1.0.7-IGB-gcc-4.9.4-Python-2.7.13
+
|353-IGB-gcc-4.9.4
|CheckM provides a set of tools for assessing the quality of genomes recovered from isolates, single cells, or metagenomes.
+
|UCSC genome browser kent bioinformatic utilities
 
|-
 
|-
|[http://sanger-pathogens.github.io/circlator/ Circlator]
+
|[http://qiime.org/ QIIME2]
|1.5.1-IGB-gcc-4.9.4-Python-3.6.1
+
|2017.10<br>2017.11<br>2017.12<br>2017.6<br>2017.8<br>2018.2<br>2018.4<br>2018.6
|A tool to circularize genome assemblies.  
+
|QIIME is an open-source bioinformatics pipeline for performing microbiome analysis from raw DNA sequencing data.
 
|-
 
|-
|[http://www.circos.ca/ Circos]
+
|[http://argtable.sourceforge.net/ argtable]
|0.69-4-IGB-gcc-4.9.4-Perl-5.24.1
+
|.2.13-IGB-gcc-4.9.4
|Circos is a software package for visualizing data and information. It visualizes data in a circular layout - this makes Circos ideal for exploring relationships between objects or positions. - Homepage: http://www.circos.ca/
+
|Argtable is an ANSI C library for parsing GNU style command line options with a minimum of fuss. - Homepage: http://argtable.sourceforge.net/
 
|-
 
|-
|[http://www.clustal.org/omega/ Clustal-Omega]
+
|[http://software.intel.com/en-us/articles/intel-tbb/ tbb]
|1.2.4-IGB-gcc-4.9.4
+
|.2017_U5-IGB-gcc-4.9.4
|Clustal Omega is a multiple sequence alignment program for proteins. It produces biologically meaningful multiple sequence alignments of divergent sequences. Evolutionary relationships can be seen via viewing Cladograms or Phylograms  - Homepage: http://www.clustal.org/omega/
+
|Intel Threading Building Blocks 4.0 (Intel TBB) is a widely used, award-winning C++ template library for creating reliable, portable, and scalable parallel applications. Use Intel TBB for a simple and rapid way of developing robust task-based parallel applications that scale to available processor cores, are compatible with multiple environments, and are easier to maintain. Intel TBB is the most proficient way to implement future-proof parallel applications that tap into the power and performance of multicore and manycore hardware platforms. - Homepage: http://software.intel.com/en-us/articles/intel-tbb/
 
|-
 
|-
|[http://www.ebi.ac.uk/Tools/msa/clustalw2/ ClustalW2]
+
|[https://github.com/simroux/VirSorter VirSorter]
|2.1-IGB-gcc-4.9.4
+
|20170215-IGB-gcc-4.9.4-Perl-5.24.1
|ClustalW2 is a general purpose multiple sequence alignment program for DNA or proteins. - Homepage: http://www.ebi.ac.uk/Tools/msa/clustalw2/
+
|VirSorter: mining viral signal from microbial genomic data.
 +
|-
 +
|[http://exon.gatech.edu/GeneMark/ GeneMarkS]
 +
|4.30-IGB-gcc-4.9.4
 +
|GeneMarkS: a self-training method for prediction of gene starts in microbial genomes
 
|-
 
|-
|[https://github.com/PacificBiosciences/ConsensusCore ConsensusCore]
+
|[http://www.gnu.org/software/gdb/gdb.html gdb]
|1.0.1-IGB-gcc-4.9.4-Python-2.7.13
+
|8.0.1-IGB-gcc-4.9.4-Python-2.7.13
|ConsensusCore is a library of C++ algorithms for PacBio multiple sequence consensus that powers Quiver (Python) and ConsensusTools (.NET).
+
|The GNU Project Debugger
 
|-
 
|-
|[http://cole-trapnell-lab.github.io/cufflinks/ Cufflinks]
+
|[https://github.com/pysam-developers/pysam Pysam]
|2.2.1<br>2.2.1-IGB-gcc-4.9.4-b4fa050
+
|0.13.0-IGB-gcc-4.9.4-Python-2.7.13<br>0.13.0-IGB-gcc-4.9.4-Python-3.6.1
|Transcript assembly, differential expression, and differential regulation for RNA-Seq
+
|Pysam is a python module for reading and manipulating Samfiles.  Its a lightweight wrapper of the samtools C-API. Pysam also includes an interface for tabix.
 
|-
 
|-
|[http://cython.org/ Cython]
+
|[https://github.com/najoshi/sabre sabre]
|0.27.3-IGB-gcc-4.9.4-Python-2.7.13
+
|20171114-IGB-gcc-4.9.4
|Cython is an optimising static compiler for both the Python programming language and the extended Cython programming language (based on Pyrex). It makes writing C extensions for Python as easy as Python itself.  
+
|Next-generation sequencing can currently produce hundreds of millions of reads per lane of sample and that number increases at a dizzying rate. Barcoding individual sequences for multiple lines or multiple species is a cost-efficient method to sequence and analyze a broad range of data.
 
|-
 
|-
 
|[https://sites.google.com/site/danposdoc/news DANPOS]
 
|[https://sites.google.com/site/danposdoc/news DANPOS]
Line 233: Line 249:
 
|A toolkit for Dynamic Analysis of Nucleosome and Protein Occupancy by Sequencing, version 2
 
|A toolkit for Dynamic Analysis of Nucleosome and Protein Occupancy by Sequencing, version 2
 
|-
 
|-
|[https://github.com/bbuchfink/diamond DIAMOND]
+
|[https://github.com/LangilleLab/microbiome_helper microbiome_helper]
|0.8.38-IGB-gcc-4.9.4<br>0.9.10-IGB-gcc-4.9.4<br>0.9.16-IGB-gcc-4.9.4<br>0.9.9-IGB-gcc-4.9.4
+
|20171114-IGB-gcc-4.9.4
|Accelerated BLAST compatible local sequence aligner
+
|An assortment of scripts to help process and automate various microbiome and metagenomic bioinformatic tools. We provide workflows, tutorials and a virtual box image to help researchers process microbial data.
 
|-
 
|-
|[http://www.broadinstitute.org/software/discovar/blog/ DISCOVARdenovo]
+
|[http://eddylab.org/infernal/ Infernal]
|52488-IGB-gcc-4.9.4
+
|1.1.2-IGB-gcc-4.9.4
|DISCOVAR de novo can generate de novo assemblies for both large and small genomes. It currently does not call variants.
+
|Infernal,INFERence of RNA ALignment, is for searching DNA sequence databases for RNA structure and sequence similarities.
 
|-
 
|-
|[http://www1.montpellier.inra.fr/CBGP/diyabc/index.php DIYABC]
+
|[http://www.netlab.uky.edu/p/bioinfo/MapSplice2 MapSplice]
|2.1.0
+
|2.2.1-IGB-gcc-4.9.4-Python-2.7.13
|a user-friendly approach to Approximate Bayesian Computation for inference on population history using molecular markers
+
|MapSplice is a software for mapping RNA-seq data to reference genome for splice junction discovery that depends only on reference genome, and not on any further annotations.
 
|-
 
|-
|[http://www.doxygen.org Doxygen]
+
|[http://opencv.org/ OpenCV]
|.1.8.13-IGB-gcc-4.9.4<br>1.8.13-IGB-gcc-4.9.4
+
|3.1.0-IGB-gcc-4.9.4-Python-2.7.13<br>3.3.0-IGB-gcc-4.9.4-Python-3.6.1
|Doxygen is a documentation system for C++, C, Java, Objective-C, Python,  IDL (Corba and Microsoft flavors), Fortran, VHDL, PHP, C#, and to some extent D. - Homepage: http://www.doxygen.org
+
|OpenCV (Open Source Computer Vision Library) is an open source computer vision and machine learning software library. OpenCV was built to provide a common infrastructure for computer vision applications and to accelerate the use of machine perception in the commercial products.
 
|-
 
|-
|[http://emboss.sourceforge.net/ EMBOSS]
+
|[http://www.ebi.ac.uk/Tools/msa/clustalw2/ ClustalW2]
|6.6.0-IGB-gcc-4.9.4-Java-1.8.0_121
+
|2.1-IGB-gcc-4.9.4
|EMBOSS, The European Molecular Biology Open Software Suite. EMBOSS is a free Open Source software analysis package specially developed for the needs of the molecular biology (e.g. EMBnet) user community.
+
|ClustalW2 is a general purpose multiple sequence alignment program for DNA or proteins. - Homepage: http://www.ebi.ac.uk/Tools/msa/clustalw2/
 
|-
 
|-
|[http://easybuilders.github.com/easybuild/ EasyBuild]
+
|[https://github.com/kundajelab/phantompeakqualtools Phantompeaktools]
|3.5.3<br>3.6.0<br>3.6.2
+
|1.2-IGB-gcc-4.9.4-R-3.4.1
|EasyBuild is a software build and installation frameworkwritten in Python that allows you to install software in a structured,repeatable and robust way.
+
|Custom SPP for Phantompeaktools
 
|-
 
|-
|[http://eigen.tuxfamily.org/index.php?title=Main_Page Eigen]
+
|[http://gnuplot.sourceforge.net/ gnuplot]
|.3.3.3-IGB-gcc-4.9.4
+
|4.6.7-IGB-gcc-4.9.4<br>5.0.6-IGB-gcc-4.9.4
|Eigen is a C++ template library for linear algebra: matrices, vectors, numerical solvers, and related algorithms. - Homepage: http://eigen.tuxfamily.org/index.php?title=Main_Page
+
|Portable interactive, function plotting utility - Homepage: http://gnuplot.sourceforge.net/
 
|-
 
|-
|[http://pb-falcon.readthedocs.io/en/latest/index.html FALCON]
+
|[http://multiqc.info/ MultiQC]
|1.8.8-IGB-gcc-4.9.4-Python-2.7.13
+
|0.9-IGB-gcc-4.9.4-Python-2.7.13<br>1.2-IGB-gcc-4.9.4-Python-2.7.13<br>1.2-IGB-gcc-4.9.4-Python-3.6.1
|FALCON is a diploid aware genome assembler designed for Pacific Biosciences long read data.
+
|MultiQC searches a given directory for analysis logs and compiles a HTML report. Its a general use tool, perfect for summarising the output from numerous bioinformatics tools.
 
|-
 
|-
|[https://github.com/PacificBiosciences/FALCON_unzip FALCON_unzip]
+
|[http://www.bcgsc.ca/platform/bioinfo/software/abyss ABySS]
|0.4.0-IGB-gcc-4.9.4-Python-2.7.13
+
|2.0.2-IGB-gcc-4.9.4
|FALCON-Unzip contains the modules that works with FALCON for full diploid assembly (representing haplotype specific contigs as "haplotigs" as assembly output).
+
|ABySS is a de novo, parallel, paired-end sequence assembler that is designed for short reads. The single-processor version is useful for assembling genomes up to 100 Mbases in size. The parallel version is implemented using MPI and is capable of assembling larger genomes.
 
|-
 
|-
|[http://hannonlab.cshl.edu/fastx_toolkit/ FASTX-Toolkit]
+
|[http://www.open-mpi.org/projects/hwloc/ hwloc]
|0.0.14-IGB-gcc-4.9.4
+
|.1.11.6-GCC-4.9.4-2.28
|The FASTX-Toolkit is a collection of command line tools for  Short-Reads FASTA/FASTQ files preprocessing. - Homepage: http://hannonlab.cshl.edu/fastx_toolkit/
+
|The Portable Hardware Locality (hwloc) software package provides a portable abstraction(across OS, versions, architectures, ...) of the hierarchical topology of modern architectures, includingNUMA memory nodes, sockets, shared caches, cores and simultaneous multithreading. It also gathers varioussystem attributes such as cache and memory information as well as the locality of I/O devices such asnetwork interfaces, InfiniBand HCAs or GPUs. It primarily aims at helping applications with gatheringinformation about modern computing hardware so as to exploit it accordingly and efficiently. - Homepage: http://www.open-mpi.org/projects/hwloc/
 
|-
 
|-
|[https://github.com/tderrien/FEELnc FEELnc]
+
|[https://github.com/google/protobuf protobuf]
|20180117-IGB-gcc-4.9.4
+
|2.6.1-IGB-gcc-4.9.4<br>3.5.0-IGB-gcc-4.9.4
|This document is intended to give a technical description of the FEELnc pipeline in order to annotate long non-coding RNAs (lncRNAs) based on reconstructed transcripts from RNA-seq data (either with or without a reference genome).  
+
|Protocol Buffers (a.k.a., protobuf) are Googles language-neutral, platform-neutral, extensible mechanism for serializing structured data.
 
|-
 
|-
|[http://www.fftw.org FFTW]
+
|[http://liulab.dfci.harvard.edu/MACS/ MACS]
|.3.3.6-gompi-4.9.4
+
|1.4.2-1-IGB-gcc-4.9.4-Python-2.7.13
|FFTW is a C subroutine library for computing the discrete Fourier transform (DFT) in one or more dimensions, of arbitrary input size, and of both real and complex data. - Homepage: http://www.fftw.org
+
|Model-based Analysis of ChIP-Seq (MACS) on short reads sequencers  such as Genome Analyzer (Illumina / Solexa). MACS empirically models the length of  the sequenced ChIP fragments, which tends to be shorter than sonication or library  construction size estimates, and uses it to improve the spatial resolution of predicted  binding sites. MACS also uses a dynamic Poisson distribution to effectively capture  local biases in the genome sequence, allowing for more sensitive and robust prediction.
 
|-
 
|-
|[https://www.ffmpeg.org/ FFmpeg]
+
|[http://nodejs.org nodejs]
|3.3-IGB-gcc-4.9.4
+
|9.9.0-IGB-gcc-4.9.4
|A complete, cross-platform solution to record, convert and stream audio and video. - Homepage: https://www.ffmpeg.org/
+
|Node.js is a platform built on Chromes JavaScript runtime  for easily building fast, scalable network applications. Node.js uses an  event-driven, non-blocking I/O model that makes it lightweight and efficient,  perfect for data-intensive real-time applications that run across distributed devices.
 
|-
 
|-
|[https://xiph.org/flac/ FLAC]
+
|[https://github.com/pgmpy/pgmpy pgmpy]
|1.3.1-IGB-gcc-4.9.4
+
|20180320-IGB-gcc-4.9.4-Python-3.6.1
|Programs and libraries for working with Free Lossless Audio Codec (FLAC) files.
+
|pgmpy is a python library for working with Probabilistic Graphical Models.
 
|-
 
|-
|[https://github.com/dstreett/FLASH2 FLASH2]
+
|[http://doc.libsodium.org/ libsodium]
|2.2.00-IGB-gcc-4.9.4
+
|1.0.13-IGB-gcc-4.9.4
|FLASH (Fast Length Adjustment of SHort reads) is an accurate and fast toolto merge paired-end reads that were generated from DNA fragments whoselengths are shorter than twice the length of reads.  Merged read pairs resultin unpaired longer reads, which are generally more desired in genomeassembly and genome analysis processes.
+
|Sodium is a modern, easy-to-use software library for encryption, decryption, signatures, password hashing and more.
 
|-
 
|-
|[https://github.com/md5sam/Falcon2Fastg Falcon2Fastg]
+
|[https://github.com/sparsehash/sparsehash sparsehash]
|0.3.1-IGB-gcc-4.9.4-Python-2.7.13
+
|2.0.3-IGB-gcc-4.9.4
|This software converts the results of PacBio assembly using FALCON, to a FASTG graph that can be visualized using Bandage.
+
|This directory contains several hash-map implementations, similar inAPI to SGIs hash_map class, but with different performance characteristics.
 
|-
 
|-
|[http://www.bioinformatics.babraham.ac.uk/projects/fastqc/ FastQC]
+
|[http://cunit.sourceforge.net/ CUnit]
|0.11.5-IGB-gcc-4.9.4-Java-1.8.0_121<br>0.11.5-IGB-gcc-4.9.4-Java-1.8.0_152
+
|2.1-3-IGB-gcc-4.9.4
|FastQC is a quality control application for high throughput sequence data. It reads in sequence data in a variety of formats and can either provide an interactive application to review the results of several different QC checks, or create an HTML based report which can be integrated into a pipeline.
+
|CUnit is a lightweight system for writing, administering, and running unit tests in C. It provides C programmers a basic testing functionality with a flexible variety of user interfaces.
 
|-
 
|-
|[http://www.microbesonline.org/fasttree/ FastTree]
+
|[http://expat.sourceforge.net/ expat]
|2.1.10-IGB-gcc-4.9.4
+
|2.2.0-IGB-gcc-4.9.4
|FastTree infers approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences. FastTree can handle alignments with up to a million of sequences in a reasonable amount of time and memory.  
+
|Expat is an XML parser library written in C. It is a stream-oriented parser in which an application registers handlers for things the parser might find in the XML document (like start tags) - Homepage: http://expat.sourceforge.net/
 
|-
 
|-
|[https://github.com/ekg/freebayes FreeBayes]
+
|[http://cole-trapnell-lab.github.io/cufflinks/ Cufflinks]
|1.1.0-IGB-gcc-4.9.4
+
|2.2.1<br>2.2.1-IGB-gcc-4.9.4-b4fa050
|FreeBayes is a Bayesian genetic variant detector designed to find small polymorphisms, specifically SNPs (single-nucleotide polymorphisms), indels (insertions and deletions), MNPs (multi-nucleotide polymorphisms), and complex events (composite insertion and substitution events) smaller than the length of a short-read sequencing alignment.
+
|Transcript assembly, differential expression, and differential regulation for RNA-Seq
 
|-
 
|-
|[http://www.broadinstitute.org/gatk/ GATK]
+
|[https://github.com/spragunr/deep_q_rl deep_q_rl]
|3.7-Java-1.8.0_121<br>3.8-0-Java-1.8.0_152<br>3.8-1-0-Java-1.8.0_152<br>4.0.4.0-IGB-gcc-4.9.4-Java-1.8.0_152-Python-3.6.1
+
|20160603-IGB-gcc-4.9.4-Python-2.7.13
|The Genome Analysis Toolkit or GATK is a software package developed at the Broad Institute to analyse next-generation resequencing data. The toolkit offers a wide variety of tools, with a primary focus on variant discovery and genotyping as well as strong emphasis on data quality assurance. Its robust architecture, powerful processing engine and high-performance computing features make it capable of taking on projects of any size.
+
|This package provides a Lasagne/Theano-based implementation of the deep Q-learning algorithm described in:Playing Atari with Deep Reinforcement Learning Volodymyr Mnih, Koray Kavukcuoglu, David Silver, Alex Graves, Ioannis Antonoglou, Daan Wierstra, Martin RiedmillerandMnih, Volodymyr, et al. "Human-level control through deep reinforcement learning." Nature 518.7540 (2015): 529-533.
 
|-
 
|-
|[http://gcc.gnu.org/ GCC]
+
|[https://rclone.org/ rclone]
|.4.9.4-2.28
+
|1.41
|The GNU Compiler Collection includes front ends for C, C++, Objective-C, Fortran, Java, and Ada, as well as libraries for these languages (libstdc++, libgcj,...). - Homepage: http://gcc.gnu.org/
+
|Rclone is a command line program to sync files and directories to and from different cloud storage
 
|-
 
|-
|[http://gcc.gnu.org/ GCCcore]
+
|[http://simplesystems.org/libtiff/ LibTIFF]
|.4.9.4<br>.7.3.0
+
|.4.0.7-IGB-gcc-4.9.4
|The GNU Compiler Collection includes front ends for C, C++, Objective-C, Fortran, Java, and Ada, as well as libraries for these languages (libstdc++, libgcj,...). - Homepage: http://gcc.gnu.org/
+
|tiff: Library and tools for reading and writing TIFF data files
 
|-
 
|-
|[http://search.cpan.org/~lds/GD/ GD]
+
|[http://jupyter.org/ jupyter]
|2.66-IGB-gcc-4.9.4-Perl-5.24.1
+
|1.0.0-IGB-gcc-4.9.4-Python-3.6.1
|GD.pm - Interface to Gd Graphics Library
+
|Project Jupyter exists to develop open-source software, open-standards, and services for interactive computing across dozens of programming languages.
 
|-
 
|-
|[http://www.gdal.org/ GDAL]
+
|[http://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=std SRA-Toolkit]
|2.3.1-IGB-gcc-4.9.4
+
|2.8.2-1
|GDAL is a translator library for raster geospatial data formats that is released under an X/MIT style Open Source license by the Open Source Geospatial Foundation. As a library, it presents a single abstract data model to the calling application for all supported formats. It also comes with a variety of useful commandline utilities for data translation and processing.
+
|The NCBI SRA Toolkit enables reading (dumping) of sequencing files from the SRA database and writing (loading) files into the .sra format  - Homepage: http://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=std
 
|-
 
|-
|[https://bitbucket.org/feeldead/gfold GFOLD]
+
|[http://tukaani.org/xz/ XZ]
|1.1.4-IGB-gcc-4.9.4
+
|.5.2.3-IGB-gcc-4.9.4
|GFOLD stands for Generalized FOLD change for ranking differentially expressed genes from RNA-seq data. GFOLD is especially useful when no replicate is available. GFOLD generalizes the fold change by considering the posterior distribution of log fold change, such that each gene is assigned a reliable fold change.
+
|xz: XZ utilities
 
|-
 
|-
|[http://www.gtk.org/ GLib]
+
|[https://mathgen.stats.ox.ac.uk/genetics_software/shapeit/shapeit.html shapeit]
|2.49.5-IGB-gcc-4.9.4
+
|2.20
|GLib is one of the base libraries of the GTK+ project - Homepage: http://www.gtk.org/
+
|SHAPEIT is a fast and accurate method for estimation of haplotypes (aka phasing) from genotype or sequencing data.
 
|-
 
|-
|[http://research-pub.gene.com/gmap/ GMAP]
+
|[http://deweylab.github.io/RSEM/ RSEM]
|2018-05-30-IGB-gcc-4.9.4
+
|1.3.0-IGB-gcc-4.9.4
|A Genomic Mapping and Alignment Program for mRNA and EST Sequences, andGSNAP: Genomic Short-read Nucleotide Alignment Program
+
|RNA-Seq by Expectation-Maximization
|-
 
|[http://research-pub.gene.com/gmap/ GMAP-GSNAP]
 
|2017-11-15-IGB-gcc-4.9.4
 
|GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences GSNAP: Genomic Short-read Nucleotide Alignment Program
 
|-
 
|[http://gmplib.org/ GMP]
 
|.6.1.2-IGB-gcc-4.9.4
 
|GMP is a free library for arbitrary precision arithmetic, operating on signed integers, rational numbers, and floating point numbers.  - Homepage: http://gmplib.org/
 
|-
 
|[https://melodi.ee.washington.edu/gmtk/ GMTK]
 
|1.4.4-IGB-gcc-4.9.4
 
|The Graphical Models Toolkit (GMTK) is an open source, publicly available toolkit for rapidly prototyping statistical models using dynamic graphical models (DGMs) and dynamic Bayesian networks (DBNs). GMTK can be used for applications and research in speech and language processing, bioinformatics, activity recognition, and any time series application. GMTK has many features, including exact and approximate inference; a large variety of built-in factors including dense, sparse, and deterministic conditional probability tables, native support for ARPA backoff-based factors and factored language models, parameter sharing, gamma and beta distributions, dense and sparse Gaussian factors, heterogeneous mixtures, deep neural network factors, and time-inhomogeneous trellis factors; arbitrary order embedded Markov chains; a GUI-based graph viewer; flexible feature-file support and processing tools (supporting pfiles, HTK files, ASCII/binary, and HDF5 files); and both offline and streaming online inference methods that can be used for both parameter learning and prediction. More information is available in the documentation. All in all, GMTK offers a flexible, concise, and expressive probabilistic modeling framework with which one may rapidly specify a vast collection of temporal statistical models.
 
 
|-
 
|-
 
|[https://wiki.gnome.org/GObjectIntrospection/ GObject-Introspection]
 
|[https://wiki.gnome.org/GObjectIntrospection/ GObject-Introspection]
Line 357: Line 361:
 
|GObject introspection is a middleware layer between C libraries (using GObject) and language bindings. The C library can be scanned at compile time and generate a metadata file, in addition to the actual native C library. Then at runtime, language bindings can read this metadata and automatically provide bindings to call into the C library.
 
|GObject introspection is a middleware layer between C libraries (using GObject) and language bindings. The C library can be scanned at compile time and generate a metadata file, in addition to the actual native C library. Then at runtime, language bindings can read this metadata and automatically provide bindings to call into the C library.
 
|-
 
|-
|[http://www.gnu.org/software/gsl/ GSL]
+
|[http://cython.org/ Cython]
|2.3-IGB-gcc-4.9.4
+
|0.27.3-IGB-gcc-4.9.4-Python-2.7.13
|The GNU Scientific Library (GSL) is a numerical library for C and C++ programmers. The library provides a wide range of mathematical routines such as random number generators, special functions and least-squares fitting. - Homepage: http://www.gnu.org/software/gsl/
+
|Cython is an optimising static compiler for both the Python programming language and the extended Cython programming language (based on Pyrex). It makes writing C extensions for Python as easy as Python itself.  
 
|-
 
|-
|[https://developer.gnome.org/gtk+/stable/ GTK+]
+
|[https://github.com/dmlc/xgboost xgboost]
|2.24.31-IGB-gcc-4.9.4-Python-2.7.13<br>2.24.31-IGB-gcc-4.9.4-Python-3.6.1
+
|0.80-IGB-gcc-4.9.4-Python-3.6.1
|The GTK+ 2 package contains libraries used for creating graphical user interfaces for applications.
+
|XGBoost is an optimized distributed gradient boosting library designed to be highly efficient, flexible and portable. It implements machine learning algorithms under the Gradient Boosting framework.
 
|-
 
|-
|[http://guidance.tau.ac.il/ver2/ GUIDANCE]
+
|[http://www.maizegenetics.net/tassel TASSEL]
|2.02-IGB-gcc-4.9.4-Perl-5.24.1
+
|5.2.28-Java-1.8.0_121
|GUIDANCE is meant to be used for weighting, filtering or masking unreliably aligned positions in sequence alignments before subsequent analysis. For example, align codon sequences (nucleotide sequences that code for proteins) using PAGAN, remove columns with low GUIDANCE scores, and use the remaining alignment to infer positive selection using the branch-site dN/dS test. Other analyses where GUIDANCE filtering could be useful include phylogeny reconstruction, reconstruction of the history of specific insertion and deletion events, inference of recombination events, etc. - Homepage: http://guidance.tau.ac.il/ver2/
+
|While TASSEL has changed considerably since its initial public release in 2001, its primary function continues to be providing tools to investigate the relationship between phenotypes and genotypes
 
|-
 
|-
|[https://developer.gnome.org/gdk-pixbuf/stable/ Gdk-Pixbuf]
+
|[https://bitbucket.org/berkeleylab/metabat MetaBAT]
|.2.36.6-IGB-gcc-4.9.4-Python-2.7.13<br>.2.36.6-IGB-gcc-4.9.4-Python-3.6.1
+
|2.12.1
|The Gdk Pixbuf is a toolkit for image loading and pixel buffer manipulation. It is used by GTK+ 2 and GTK+ 3 to load and manipulate images. In the past it was distributed as part of GTK+ 2 but it was split off into a separate package in preparation for the change to GTK+ 3.
+
|MetaBAT, an efficient tool for accurately reconstructing single genomes from complex microbial communities
 
|-
 
|-
|[http://exon.gatech.edu/GeneMark/ GeneMark-ES]
+
|[https://github.com/hellbelly/BS-Snper BS-Snper]
|4.33-IGB-gcc-4.9.4-Perl-5.24.1<br>4.33-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
+
|20170222-IGB-gcc-4.9.4-Perl-5.24.1
|Novel genomes can be analyzed by the program GeneMark-ES utilizing unsupervised training.
+
|BS-SNPer is an ultrafast and memory-efficient package, a program for BS-Seq variation detection from alignments in standard BAM/SAM format using approximate Bayesian modeling.
 
|-
 
|-
|[http://exon.gatech.edu/GeneMark/ GeneMarkS]
+
|[http://compression.ca/pbzip2/ pbzip2]
|4.30-IGB-gcc-4.9.4
+
|1.1.13-IGB-gcc-4.9.4
|GeneMarkS: a self-training method for prediction of gene starts in microbial genomes
+
|PBZIP2 is a parallel implementation of the bzip2 block-sorting file compressor that uses pthreads and achieves near-linear speedup on SMP machines.
 
|-
 
|-
|[https://github.com/PacificBiosciences/GenomicConsensus GenomicConsensus]
+
|[http://www.regulatory-genomics.org/rgt/basic-introduction/ RGT]
|3.0.2-IGB-gcc-4.9.4-Python-2.7.13
+
|0.11.3-IGB-gcc-4.9.4-Python-2.7.13
|The GenomicConsensus package provides the variantCaller tool, which allows you to apply the Quiver or Arrow algorithm to mapped PacBio reads to get consensus and variant calls.
+
|Regulatory Genomics Toolbox (RGT) is an open source python library for analysis of regulatory genomics. RGT is programmed in an oriented object fashion and its core classes provide functionality for handling regulatory genomics data.  
 
|-
 
|-
|[http://ghostscript.com GhostScript]
+
|[https://github.com/TGAC/KAT KAT]
|9.21-IGB-gcc-4.9.4
+
|2.4.1-IGB-gcc-4.9.4
|Ghostscript is a versatile processor for PostScript data with the ability to render PostScript to different targets. It used to be part of the cups printing stack, but is no longer used for that. - Homepage: http://ghostscript.com
+
|KAT is a suite of tools that analyse jellyfish hashes or sequence files (fasta or fastq) using kmer counts.  
 
|-
 
|-
|[https://gradle.org Gradle]
+
|VICSIN
|4.7
+
|0.5-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13<br>0.5.1-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13<br>0.5.2-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
|Complete Gradle install.From mobile apps to microservices, from small startups to big enterprises,Gradle helps teams build, automate and deliver better software, faster.
+
|VICSIN = Viral, Integrative, and Conjugative Sequence Identification and Networking
 
|-
 
|-
|[http://www.graphicsmagick.org/ GraphicsMagick]
+
|[http://www.netlib.org/scalapack/ ScaLAPACK]
|1.3.26-IGB-gcc-4.9.4
+
|.2.0.2-gompi-4.9.4-OpenBLAS-0.2.19-LAPACK-3.7.0
|GraphicsMagick is the swiss army knife of image processing.
+
|The ScaLAPACK (or Scalable LAPACK) library includes a subset of LAPACK routines redesigned for distributed memory MIMD parallel computers. - Homepage: http://www.netlib.org/scalapack/
 
|-
 
|-
|[http://www.gurobi.com/ Gurobi]
+
|[http://www.clustal.org/omega/ Clustal-Omega]
|7.5.2
+
|1.2.4-IGB-gcc-4.9.4
|The Gurobi Optimizer was designed from the ground up to be the fastest, most powerful solver available for your LP, QP, QCP, and MIP (MILP, MIQP, and MIQCP) problems.
+
|Clustal Omega is a multiple sequence alignment program for proteins. It produces biologically meaningful multiple sequence alignments of divergent sequences. Evolutionary relationships can be seen via viewing Cladograms or Phylograms  - Homepage: http://www.clustal.org/omega/
 
|-
 
|-
|[http://www.hdfgroup.org/HDF5/ HDF5]
+
|[https://github.com/lisa-lab/pylearn2 pylearn2]
|1.8.18-IGB-gcc-4.9.4
+
|20170525-IGB-gcc-4.9.4-Python-2.7.13
|HDF5 is a unique technology suite that makes possible the management of extremely large and complex data collections.
+
|Pylearn2 is a library designed to make machine learning research easy. - Homepage: https://github.com/lisa-lab/pylearn2
 
|-
 
|-
|[https://ccb.jhu.edu/software/hisat2/index.shtml HISAT2]
+
|[http://gmplib.org/ GMP]
|2.0.5-IGB-gcc-4.9.4
+
|.6.1.2-IGB-gcc-4.9.4
|HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) against the general human population (as well as against a single reference genome). - Homepage: https://ccb.jhu.edu/software/hisat2/index.shtml
+
|GMP is a free library for arbitrary precision arithmetic, operating on signed integers, rational numbers, and floating point numbers. - Homepage: http://gmplib.org/
 
|-
 
|-
|[http://hmmer.org/ HMMER]
+
|[https://github.com/tderrien/FEELnc FEELnc]
|2.3.2-IGB-gcc-4.9.4<br>3.1b2-IGB-gcc-4.9.4<br>3.2.1-IGB-gcc-4.9.4
+
|20180117-IGB-gcc-4.9.4
|HMMER is used for searching sequence databases for homologs of protein sequences, and for making protein sequence alignments. It implements methods using probabilistic models called profile hidden Markov models (profile HMMs).  Compared to BLAST, FASTA, and other sequence alignment and database search tools based on older scoring methodology, HMMER aims to be significantly more accurate and more able to detect remote homologs because of the strength of its underlying mathematical models. In the past, this strength came at significant computational expense, but in the new HMMER3 project, HMMER is now essentially as fast as BLAST.
+
|This document is intended to give a technical description of the FEELnc pipeline in order to annotate long non-coding RNAs (lncRNAs) based on reconstructed transcripts from RNA-seq data (either with or without a reference genome).  
 
|-
 
|-
|[http://homer.ucsd.edu/homer/ HOMER]
+
|[http://oss.sgi.com/projects/libnuma/ numactl]
|4.9.1-IGB-gcc-4.9.4-Perl-5.24.1
+
|.2.0.11-GCC-4.9.4-2.28
|HOMER (Hypergeometric Optimization of Motif EnRichment) is a suite of tools for Motif Discovery and ChIP-Seq analysis. It is a collection of command line programs for unix-style operating systems written in mostly perl and c++. Homer was primarily written as a de novo motif discovery algorithm that is well suited for finding 8-12 bp motifs in large scale genomics data.
+
|The numactl program allows you to run your application program on specific cpus and memory nodes.It does this by supplying a NUMA memory policy to the operating system before running your program.The libnuma library provides convenient ways for you to add NUMA memory policies into your own program. - Homepage: http://oss.sgi.com/projects/libnuma/
 
|-
 
|-
|[http://www-huber.embl.de/users/anders/HTSeq/ HTSeq]
+
|[http://cairographics.org cairo]
|0.9.0-IGB-gcc-4.9.4-Python-2.7.13<br>0.9.1-IGB-gcc-4.9.4-Python-2.7.13
+
|1.14.8-IGB-gcc-4.9.4
|A framework to process and analyze data from high-throughput sequencing (HTS) assays
+
|Cairo is a 2D graphics library with support for multiple output devices. Currently supported output targets include the X Window System (via both Xlib and XCB), Quartz, Win32, image buffers, PostScript, PDF, and SVG file output. Experimental backends include OpenGL, BeOS, OS/2, and DirectFB - Homepage: http://cairographics.org
 
|-
 
|-
|[http://www.htslib.org/ HTSlib]
+
|[http://www.gtk.org/ GLib]
|1.3.1-IGB-gcc-4.9.4<br>1.4-IGB-gcc-4.9.4<br>1.5-IGB-gcc-4.9.4
+
|2.49.5-IGB-gcc-4.9.4
|A C library for reading/writing high-throughput sequencing data. This package includes the utilities bgzip and tabix
+
|GLib is one of the base libraries of the GTK+ project - Homepage: http://www.gtk.org/
 
|-
 
|-
|[http://huttenhower.sph.harvard.edu/humann2 HUMAnN2]
+
|[http://www.tcl.tk/ Tk]
|0.11.1-IGB-gcc-4.9.4-Python-3.6.1
+
|.8.6.6-IGB-gcc-4.9.4
|HUMAnN is a pipeline for efficiently and accurately profiling the presence/absence and abundance of microbial pathways in a community from metagenomic or metatranscriptomic sequencing data (typically millions of short DNA/RNA reads). This process, referred to as functional profiling, aims to describe the metabolic potential of a microbial community and its members. More generally, functional profiling answers the question "What are the microbes in my community-of-interest doing (or capable of doing)?"
+
|Tk is an open source, cross-platform widget toolchain that provides a library of basic elements for building a graphical user interface (GUI) in many different programming languages. - Homepage: http://www.tcl.tk/
 
|-
 
|-
|[http://www.freedesktop.org/wiki/Software/HarfBuzz HarfBuzz]
+
|[http://lasagne.readthedocs.io/en/latest/index.html Lasagne]
|.1.4.6-IGB-gcc-4.9.4
+
|20170606-IGB-gcc-4.9.4-Python-2.7.13
|HarfBuzz is an OpenType text shaping engine. - Homepage: http://www.freedesktop.org/wiki/Software/HarfBuzz
+
|Lasagne is a lightweight library to build and train neural networks in Theano. - Homepage: http://lasagne.readthedocs.io/en/latest/index.html
 
|-
 
|-
|[https://github.com/nservant/HiC-Pro HiC-Pro]
+
|[http://deeplearning.net/software/libgpuarray/ libgpuarray]
|2.9.0-IGB-gcc-4.9.4-Python-2.7.13
+
|0.6.5-IGB-gcc-4.9.4
|HiC-Pro was designed to process Hi-C data, from raw fastq files (paired-end Illumina data) to the normalized contact maps. Since version 2.7.0, HiC-Pro supports the main Hi-C protocols, including digestion protocols as well as protocols that do not require restriction enzyme such as DNase Hi-C.
+
|Make a common GPU ndarray(n dimensions array) that can be reused by all projects that is as future proof as possible, while keeping it easy to use for simple need/quick test. - Homepage: http://deeplearning.net/software/libgpuarray/
 
|-
 
|-
|[https://github.com/kundajelab/idr IDR]
+
|[http://www.pango.org/ Pango]
|2.0.4-IGB-gcc-4.9.4-Python-3.6.1
+
|.1.40.6-IGB-gcc-4.9.4
|The IDR (Irreproducible Discovery Rate) framework is a unified approach to measure the reproducibility of findings identified from replicate experiments and provide highly stable thresholds based on reproducibility. Unlike the usual scalar measures of reproducibility, the IDR approach creates a curve, which quantitatively assesses when the findings are no longer consistent across replicates. In laymans terms, the IDR method compares a pair of ranked lists of identifications (such as ChIP-seq peaks).
+
|Pango is a library for laying out and rendering of text, with an emphasis on internationalization.Pango can be used anywhere that text layout is needed, though most of the work on Pango so far has been done in thecontext of the GTK+ widget toolkit. Pango forms the core of text and font handling for GTK+-2.x. - Homepage: http://www.pango.org/
 
|-
 
|-
|IGB-gcc
+
|[http://www.lysator.liu.se/~nisse/nettle/ nettle]
|.4.9.4
+
|3.3-IGB-gcc-4.9.4
|GNU Compiler Collection (GCC) based compiler toolchain, including OpenMPI for MPI support, OpenBLAS (BLAS and LAPACK support), FFTW and ScaLAPACK.
+
|Nettle is a cryptographic library that is designed to fit easily in more or less any context: In crypto toolkits for object-oriented languages (C++, Python, Pike, ...), in applications like LSH or GNUPG, or even in kernel space.
 
|-
 
|-
|[https://github.com/pjeraldo/imtornado2 IM-TORNADO]
+
|[https://github.com/LLNL/ior ior]
|2.0.3.3-IGB-gcc-4.9.4-Python-2.7.13
+
|3.0.1-IGB-gcc-4.9.4
|A pipeline for 16S reads from paired-end libraries
+
|Parallel filesystem I/O benchmark
 
|-
 
|-
|[http://ipython.org/index.html IPython]
+
|[https://cran.r-project.org/web/packages/RcppGSL/index.html RcppGSL]
|5.3.0-IGB-gcc-4.9.4-Python-3.6.1
+
|0.3.2-IGB-gcc-4.9.4-R-3.3.3
|IPython provides a rich architecture for interactive computing with: Powerful interactive shells (terminal and Qt-based). A browser-based notebook with support for code, text, mathematical expressions, inline plots and other rich media. Support for interactive data visualization and use of GUI toolkits. Flexible, embeddable interpreters to load into your own projects. Easy to use, high performance tools for parallel computing.
+
|Rcpp integration for GNU GSL vectors and matrices The GNU Scientific Library (or GSL) is a collection of numerical routines for scientific computing. It is particularly useful for C and C++ programs as it provides a standard C interface to a wide range of mathematical routines. There are over 1000 functions in total with an extensive test suite. The RcppGSL package provides an easy-to-use interface between GSL data structures and R using concepts from Rcpp which is itself a package that eases the interfaces between R and C++. This package also serves as a prime example of how to build a package that uses Rcpp to connect to another third-party library. The autoconf script, inline plugin and example package can all be used as a stanza to write a similar package against another library.
 
|-
 
|-
|[https://databank.illinois.edu/ IllinoisDataBank]
+
|[https://www.gnu.org/software/help2man/ help2man]
|1.0-IGB-gcc-4.9.4-Python-2.7.13
+
|.1.47.4<br>.1.47.4-GCCcore-4.9.4<br>.1.47.4-GCCcore-7.3.0
|The Illinois Data Bank is a public access repository for publishing research data from the University of Illinois at Urbana-Champaign - Homepage: https://databank.illinois.edu/
+
|help2man produces simple manual pages from the --help and --version output of other commands.
 
|-
 
|-
|[http://www.imagemagick.org/ ImageMagick]
+
|[https://github.com/barricklab/breseq breseq]
|7.0.5-5-IGB-gcc-4.9.4
+
|0.31.0-IGB-gcc-4.9.4
|ImageMagick is a software suite to create, edit, compose, or convert bitmap images - Homepage: http://www.imagemagick.org/
+
|is a computational pipeline for the analysis of short-read re-sequencing data (e.g. Illumina, 454, IonTorrent, etc.). It uses reference-based alignment approaches to predict mutations in a sample relative to an already sequenced genome.
 
|-
 
|-
|[http://eddylab.org/infernal/ Infernal]
+
|[https://www.tensorflow.org/ Tensorflow-GPU]
|1.1.2-IGB-gcc-4.9.4
+
|1.2.1-IGB-gcc-4.9.4-Python-3.6.1<br>1.5.1-IGB-gcc-4.9.4-Python-3.6.1
|Infernal,INFERence of RNA ALignment, is for searching DNA sequence databases for RNA structure and sequence similarities.
+
|An open-source software library for Machine Intelligence
 
|-
 
|-
|[https://www.ebi.ac.uk/interpro/interproscan.html InterProScan]
+
|[https://www.rosettacommons.org/ rosetta]
|5.27-66.0-IGB-gcc-4.9.4-Java-1.8.0_152<br>5.28-67.0-IGB-gcc-4.9.4-Java-1.8.0_152
+
|2017.52-IGB-gcc-4.9.4
|InterProScan is the software package that allows sequences (protein and nucleic) to be scanned against InterPros signatures. Signatures are predictive models, provided by several different databases, that make up the InterPro consortium.
+
|The Rosetta software suite includes algorithms for computational modeling and analysis of protein structures.  
 
|-
 
|-
|[http://sourceforge.net/projects/junit JUnit]
+
|[http://www.bzip.org/ bzip2]
|4.12-Java-1.8.0_121
+
|1.0.6-IGB-gcc-4.9.4
|A programmer-oriented testing framework for Java.
+
|bzip2 is a freely available, patent free, high-quality data compressor. It typically compresses files to within 10% to 15% of the best available techniques (the PPM family of statistical compressors), whilst being around twice as fast at compression and six times faster at decompression. - Homepage: http://www.bzip.org/
 
|-
 
|-
|[http://www.ece.uvic.ca/~frodo/jasper/ JasPer]
+
|[https://www.seqan.de/ seqan]
|1.900.1-IGB-gcc-4.9.4<br>2.0.10-IGB-gcc-4.9.4
+
|2.3.2-IGB-gcc-4.9.4
|The JasPer Project is an open-source initiative to provide a free software-based reference implementation of the codec specified in the JPEG-2000 Part-1 standard. - Homepage: http://www.ece.uvic.ca/~frodo/jasper/
+
|SeqAn is an open source C++ library of efficient algorithms and data structures for the analysis of sequences with the focus on biological data
 
|-
 
|-
|[http://java.com/ Java]
+
|[http://exon.gatech.edu/GeneMark/ GeneMark-ES]
|1.8.0_121<br>1.8.0_152
+
|4.33-IGB-gcc-4.9.4-Perl-5.24.1<br>4.33-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
|Java Platform, Standard Edition (Java SE) lets you develop and deploy Java applications on desktops and servers. - Homepage: http://java.com/
+
|Novel genomes can be analyzed by the program GeneMark-ES utilizing unsupervised training.
 
|-
 
|-
|[http://www.genome.umd.edu/jellyfish.html Jellyfish]
+
|[http://www.numpy.org numpy]
|1.1.12-IGB-gcc-4.9.4<br>2.2.6-IGB-gcc-4.9.4
+
|1.14.1-IGB-gcc-4.9.4-Python-3.6.1
|Jellyfish is a tool for fast, memory-efficient counting of k-mers in DNA. - Homepage: http://www.genome.umd.edu/jellyfish.html
+
|NumPy is the fundamental package for scientific computing with Python. It contains among other things: a powerful N-dimensional array object, sophisticated (broadcasting) functions, tools for integrating C/C++ and Fortran code, useful linear algebra, Fourier transform, and random number capabilities. Besides its obvious scientific uses, NumPy can also be used as an efficient multi-dimensional container of generic data. Arbitrary data-types can be  defined. This allows NumPy to seamlessly and speedily integrate with a wide variety of databases.
 
|-
 
|-
|[https://github.com/TGAC/KAT KAT]
+
|[https://github.com/neufeld/pandaseq PANDAseq]
|2.4.1-IGB-gcc-4.9.4
+
|2.11-IGB-gcc-4.9.4
|KAT is a suite of tools that analyse jellyfish hashes or sequence files (fasta or fastq) using kmer counts.  
+
|PANDAseq assembles Illumina Solexa overlapping pair-end reads. - Homepage: https://github.com/neufeld/pandaseq
 
|-
 
|-
|[https://github.com/fchollet/keras Keras]
+
|[http://bioinf.uni-greifswald.de/augustus/ augustus]
|2.0.6-IGB-gcc-4.9.4-Python-2.7.13<br>2.0.8-IGB-gcc-4.9.4-Python-3.6.1<br>2.1.2-IGB-gcc-4.9.4-Python-3.6.1<br>2.1.5-IGB-gcc-4.9.4-Python-3.6.1<br>2.2.0-IGB-gcc-4.9.4-Python-3.6.1
+
|3.2.3-IGB-gcc-4.9.4
|Keras is a high-level neural networks API, written in Python and capable of running on top of TensorFlow, CNTK, or Theano.  
+
|AUGUSTUS is a program that predicts genes in eukaryotic genomic sequences.  - Homepage: http://bioinf.uni-greifswald.de/augustus/
 
|-
 
|-
|[https://ccb.jhu.edu/software/kraken/ Kraken]
+
|[http://www.cbs.dtu.dk/cgi-bin/nph-sw_request?tmhmm TMHMM]
|1.0-IGB-gcc-4.9.4
+
|2.0c-IGB-gcc-4.9.4
|Kraken is a system for assigning taxonomic labels to short DNA sequences, usually obtained through metagenomic studies. Previous attempts by other bioinformatics software to accomplish this task have often used sequence alignment or machine learning techniques that were quite slow, leading to the development of less sensitive but much faster abundance estimation programs.
+
|Transmembrane helices in proteins
 
|-
 
|-
|[https://github.com/marbl/Krona Krona]
+
|[ftp://ftp.ebi.ac.uk/pub/databases/Pfam/Tools/README pfamscan]
|2.7-IGB-gcc-4.9.4-Perl-5.24.1
+
|1.6-IGB-gcc-4.9.4-Perl-5.24.1
|Interactively explore metagenomes and more from a web browser.
+
|This readme should help you get started with "pfam_scan.pl", which is for usewith the HMMER3 version of HMMER.
 
|-
 
|-
|[http://lame.sourceforge.net/ LAME]
+
|[https://support.10xgenomics.com/genome-exome/software/visualization/latest/what-is-loupe loupe]
|3.99.5-IGB-gcc-4.9.4
+
|2.1.1
|LAME is a high quality MPEG Audio Layer III (MP3) encoder licensed under the LGPL.
+
|Loupe is a genome browser designed to visualize the Linked-Read data produced by the 10x Chromium Platform. Loupe is named for a jewelers loupe, which is used to inspect gems.
 
|-
 
|-
|[http://www.bx.psu.edu/~rsharris/lastz/ LASTZ]
+
|[https://mariadb.org/ MariaDB]
|1.04.00-IGB-gcc-4.9.4
+
|10.1.31-IGB-gcc-4.9.4<br>5.5.58-IGB-gcc-4.9.4
|LASTZ is a program for aligning DNA sequences, a pairwise aligner. Originally designed to handle sequences the size of human chromosomes and from different species, it is also useful for sequences produced by NGS  sequencing technologies such as Roche 454. - Homepage: http://www.bx.psu.edu/~rsharris/lastz/
+
|MariaDB An enhanced, drop-in replacement for MySQL.
 
|-
 
|-
|[http://www.bcgsc.ca/platform/bioinfo/software/links LINKS]
+
|[http://www1.montpellier.inra.fr/CBGP/software/GeneClass/ geneclass]
|1.8.5-IGB-gcc-4.9.4-Perl-5.24.1
+
|2.0
|LINKS is a scalable genomics application for scaffolding or re-scaffolding genome assembly drafts with long reads, such as those produced by Oxford Nanopore Technologies Ltd and Pacific Biosciences. It provides a generic alignment-free framework for scaffolding and can work on any sequences. It is versatile and supports not only long sequences as a source of long-range information, but also MPET pairs and linked-reads, such as those from the 10X Genomics GemCode and Chromium platform, via ARCS (http://www.bcgsc.ca/platform/bioinfo/software/arcs). Fill gaps in LINKS-derived scaffolds using Sealer (http://www.bcgsc.ca/platform/bioinfo/software/sealer).
+
|GeneClass2 is a program employing multilocus genotypes to select or exclude populations as origins of individuals (Assignment and Migrants Detection). This is a completely rewritten new version that includes pop100gene features.
 
|-
 
|-
|[http://llvm.org/ LLVM]
+
|[http://www.biostat.jhsph.edu/~hji/cisgenome/ cisgenome]
|4.0.1-IGB-gcc-4.9.4<br>6.0.0-IGB-gcc-4.9.4
+
|2.0-IGB-gcc-4.9.4
|The LLVM Core libraries provide a modern source- and target-independent optimizer, along with code generation support for many popular CPUs (as well as some less common ones!) These libraries are built around a well specified code representation known as the LLVM intermediate representation ("LLVM IR"). The LLVM Core libraries are well documented, and it is particularly easy to invent your own language (or port an existing compiler) to use LLVM as an optimizer and code generator.
+
|An integrated tool for tiling array, ChIP-seq, genome and cis-regulatory element analysis
 
|-
 
|-
|[https://symas.com/lmdb LMDB]
+
|[Complete rewrite of the NASM assembler with BSD license - Homepage: http://www.tortall.net/projects/yasm/ Yasm]
|0.9.22-IGB-gcc-4.9.4
+
|.1.3.0-IGB-gcc-4.9.4<br>1.3.0-IGB-gcc-4.9.4
|LMDB is a fast, memory-efficient database. With memory-mapped files, it has the read performance of a pure in-memory database while retaining the persistence of standard disk-based databases.
+
|Yasm: Complete rewrite of the NASM assembler with BSD license - Homepage: http://www.tortall.net/projects/yasm/
 
|-
 
|-
|[http://lasagne.readthedocs.io/en/latest/index.html Lasagne]
+
|[https://github.com/PacificBiosciences/blasr BLASR]
|20170606-IGB-gcc-4.9.4-Python-2.7.13
+
|4.0.0-IGB-gcc-4.9.4
|Lasagne is a lightweight library to build and train neural networks in Theano. - Homepage: http://lasagne.readthedocs.io/en/latest/index.html
+
|BLASR (Basic Local Alignment with Successive Refinement) rapidly maps  reads to genomes by finding the highest scoring local alignment or set of local alignments  between the read and the genome. Optimized for PacBios extraordinarily long reads and  taking advantage of rich quality values, BLASR maps reads rapidly with high accuracy.  
 
|-
 
|-
|[http://simplesystems.org/libtiff/ LibTIFF]
+
|[http://microbiomeutil.sourceforge.net/ microbiomeutil]
|.4.0.7-IGB-gcc-4.9.4
+
|20110519-IGB-gcc-4.9.4
|tiff: Library and tools for reading and writing TIFF data files
+
|Contains ChimeraSlayer, WigeoN, and NAST-iEr
 
|-
 
|-
|[http://sourceforge.net/projects/libuuid/ LibUUID]
+
|[http://wasabiapp.org/software/prank/ PRANK]
|1.0.3-IGB-gcc-4.9.4
+
|170427-IGB-gcc-4.9.4
|Portable uuid C library
+
|PRANK is a probabilistic multiple alignment program for DNA, codon and amino-acid sequences. It’s based on a novel algorithm that treats insertions correctly and avoids over-estimation of the number of deletion events. In addition, PRANK borrows ideas from maximum likelihood methods used in phylogenetics and correctly takes into account the evolutionary distances between sequences. Lastly, PRANK allows for defining a potential structure for sequences to be aligned and then, simultaneously with the alignment, predicts the locations of structural units in the sequences.
 
|-
 
|-
|[http://www.littlecms.com/ LittleCMS]
+
|[https://gdc.cancer.gov/access-data/gdc-data-transfer-tool gdc-client]
|.2.8-IGB-gcc-4.9.4<br>2.8-IGB-gcc-4.9.4
+
|1.3.0-IGB-gcc-4.9.4-Python-2.7.13
|Little CMS intends to be an OPEN SOURCE small-footprint color management engine, with special focus on accuracy and performance.  - Homepage: http://www.littlecms.com/
+
|The GDC Data Transfer Tool Client provides a command-line interface supporting both GDC data downloads and submissions.
 
|-
 
|-
|[http://www.lua.org/ Lua]
+
|[https://github.com/kundajelab/phantompeakqualtools Phantompeaktools-spp]
|5.1.5-IGB-gcc-4.9.4<br>5.3.4-IGB-gcc-4.9.4
+
|.1.2-IGB-gcc-4.9.4-R-3.4.1
|Lua is a powerful, fast, lightweight, embeddable scripting language. Lua combines simple procedural syntax with powerful data description constructs based on associative arrays and extensible semantics. Lua is dynamically typed, runs by interpreting bytecode for a register-based virtual machine, and has automatic memory management with incremental garbage collection, making it ideal for configuration, scripting, and rapid prototyping.
+
|Custom SPP for Phantompeaktools
 
|-
 
|-
|[http://www.gnu.org/software/m4/m4.html M4]
+
|[http://www.makotemplates.org Mako]
|.1.4.17-IGB-gcc-4.9.4<br>.1.4.18<br>.1.4.18-GCCcore-4.9.4<br>.1.4.18-IGB-gcc-4.9.4
+
|1.0.6-IGB-gcc-4.9.4-Python-3.6.1
|GNU M4 is an implementation of the traditional Unix macro processor. It is mostly SVR4 compatible  although it has some extensions (for example, handling more than 9 positional parameters to macros). GNU M4 also has built-in functions for including files, running shell commands, doing arithmetic, etc.
+
|A super-fast templating language that borrows the best ideas from the existing templating languages
 
|-
 
|-
|[http://liulab.dfci.harvard.edu/MACS/ MACS]
+
|[http://bioinformatics.psb.ugent.be/supplementary_data/erbon/nov2003/ randfold]
|1.4.2-1-IGB-gcc-4.9.4-Python-2.7.13
+
|2.0.1-IGB-gcc-4.9.4
|Model-based Analysis of ChIP-Seq (MACS) on short reads sequencers  such as Genome Analyzer (Illumina / Solexa). MACS empirically models the length of  the sequenced ChIP fragments, which tends to be shorter than sonication or library  construction size estimates, and uses it to improve the spatial resolution of predicted  binding sites. MACS also uses a dynamic Poisson distribution to effectively capture  local biases in the genome sequence, allowing for more sensitive and robust prediction.
+
|Minimum free energy of folding randomization test software
 
|-
 
|-
|[https://github.com/taoliu/MACS/ MACS2]
+
|[http://www.genetics.ucla.edu/software/admixture/index.html admixture]
|2.1.1.20160309-IGB-gcc-4.9.4-Python-2.7.13
+
|1.3.0
|Model Based Analysis for ChIP-Seq data - Homepage: https://github.com/taoliu/MACS/
+
|ADMIXTURE is a software tool for maximum likelihood estimation of individual ancestries from multilocus SNP genotype datasets. It uses the same statistical model as STRUCTURE but calculates estimates much more rapidly using a fast numerical optimization algorithm.  
 
|-
 
|-
|[http://mafft.cbrc.jp/alignment/software/ MAFFT]
+
|shortbred/beta
|7.310-IGB-gcc-4.9.4
+
|beta
|MAFFT is a multiple sequence alignment program  for unix-like operating systems.  It offers a range of multiple alignment methods, L-INS-i (accurate; for alignment of <∼200 sequences),  FFT-NS-2 (fast; for alignment of <∼10,000 sequences), etc. - Homepage: http://mafft.cbrc.jp/alignment/software/
+
|
 
|-
 
|-
|[http://www.yandell-lab.org/software/maker.html MAKER]
+
|[https://lftp.yar.ru/ lftp]
|2.31.9-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded<br>3.00.0-beta-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded<br>3.01.1-beta-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
+
|4.8.3
|MAKER is a portable and easily configurable genome annotation pipeline. Its purpose is to allow smaller eukaryotic and prokaryotic genome projects to independently annotate their genomes and to create genome databases. MAKER identifies repeats, aligns ESTs and proteins to a genome, produces ab-initio gene predictions and automatically synthesizes these data into gene annotations having evidence-based quality values. MAKER is also easily trainable: outputs of preliminary runs can be used to automatically retrain its gene prediction algorithm, producing higher quality gene-models on seusequent runs. MAKERs inputs are minimal and its ouputs can be directly loaded into a GMOD database. They can also be viewed in the Apollo genome browser; this feature of MAKER provides an easy means to annotate, view and edit individual contigs and BACs without the overhead of a database. MAKER should prove especially useful for emerging model organism projects with minimal bioinformatics expertise and computer resources.
+
|FTP is a sophisticated file transfer program supporting a number of network protocols (ftp, http, sftp, fish, torrent).  
 
|-
 
|-
|[https://github.com/LynchLab/MAPGD MAPGD]
+
|[https://www.ebi.ac.uk/~zerbino/velvet/ velvet]
|0.4.26-IGB-gcc-4.9.4
+
|1.2.10-IGB-gcc-4.9.4-kmer_121
|MAPGD is a series of related programs that estimate allele frequency, heterozygosity, Hardy-Weinberg disequilibrium, linkage disequilibrium and identity-by-descent (IBD) coefficients from population genomic data using a statistically rigorous maximum likelihood approach.
+
|Velvet is a de novo genomic assembler specially designed for short read sequencing technologies, such as Solexa or 454, developed by Daniel Zerbino and Ewan Birney at the European Bioinformatics Institute (EMBL-EBI), near Cambridge, in the United Kingdom.  
 
|-
 
|-
|[http://www.mathworks.com/products/matlab MATLAB]
+
|[http://opendap.org/download/libdap libdap]
|2017a<br>2017b
+
|.3.19.1-IGB-gcc-4.9.4
|MATLAB is a high-level language and interactive environment that enables you to perform computationally intensive tasks faster than with traditional programming languages such as C, C++, and Fortran.
+
|A C++ SDK which contains an implementation of DAP 2.0 and the development versions of DAP3, up to 3.4. This includes both Client- and Server-side support classes.
 
|-
 
|-
|[https://www.mathworks.com/help/matlab/matlab-engine-for-python.html MATLAB-python]
+
|[http://lbzip2.org/ lbzip2]
|2017b-IGB-gcc-4.9.4-Python-3.6.1
+
|2.5-IGB-gcc-4.9.4
|The MATLAB Engine API for Python provides a package for Python to call MATLAB as a computational engine. The engine supports the reference implementation (CPython) for Python versions 2.7, 3.5, and 3.6.
+
|lbzip2 is a free, multi-threaded compression utility with support for bzip2 compressed file format.
 
|-
 
|-
|[http://micans.org/mcl/ MCL]
+
|[https://github.com/shenlab-sinai/diffreps diffReps]
|14.137-IGB-gcc-4.9.4
+
|1.55.6-IGB-gcc-4.9.4-Perl-5.24.1
|The MCL algorithm is short for the Markov Cluster Algorithm, a fastand scalable unsupervised cluster algorithm for graphs (also known as networks) basedon simulation of (stochastic) flow in graphs. - Homepage: http://micans.org/mcl/
+
|ChIP-seq is now widely used to profile the protein DNA interactions on a genome. It is of high interest to compare the differential enrichment of a histone mark or transcription factor between two contrasting conditions, such as disease vs. control. diffReps is developed to serve this purpose. It scans the whole genome using a sliding window, performing millions of statistical tests and report the significant hits. - Homepage: https://github.com/shenlab-sinai/diffreps
 
|-
 
|-
|[https://github.com/voutcn/megahit MEGAHIT]
+
|[https://github.com/PacificBiosciences/ConsensusCore ConsensusCore]
|1.1.1-IGB-gcc-4.9.4
+
|1.0.1-IGB-gcc-4.9.4-Python-2.7.13
|MEGAHIT is a single node assembler for large and complex metagenomics NGS reads, such as soil. It makes use of succinct de Bruijn graph (SdBG) to achieve low memory assembly. - Homepage: https://github.com/voutcn/megahit
+
|ConsensusCore is a library of C++ algorithms for PacBio multiple sequence consensus that powers Quiver (Python) and ConsensusTools (.NET).
 
|-
 
|-
|[http://ab.inf.uni-tuebingen.de/software/megan6/ MEGAN]
+
|efishared
|6.12.2-Java-1.8.0_152
+
|beta<br>beta_private<br>devel<br>devlocal<br>prod<br>prod_private
|MEGAN6 is a comprehensive toolbox for interactively analyzing microbiome data. All the interactive tools you need in one application.
+
|
 
|-
 
|-
|[http://meme-suite.org/ MEME]
+
|[http://rna.urmc.rochester.edu/RNAstructure.html RNAstructure]
|4.12.0-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13<br>5.0.1-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
+
|6.0-IGB-gcc-4.9.4
|The MEME Suite allows you to: * discover motifs using MEME, DREME (DNA only) or  GLAM2 on groups of related DNA or protein sequences, * search sequence databases with motifs using  MAST, FIMO, MCAST or GLAM2SCAN, * compare a motif to all motifs in a database of motifs, * associate  motifs with Gene Ontology terms via their putative target genes, and * analyse motif enrichment  using SpaMo or CentriMo.
+
|RNAstructure is a complete package for RNA and DNA secondary structure prediction and analysis. It includes algorithms for secondary structure prediction, including facility to predict base pairing probabilities.  
 
|-
 
|-
|[http://www.mpich.org/ MPICH]
+
|[https://github.com/arq5x/bedtools2 BEDTools]
|3.0.4-GCC-4.9.4-2.28
+
|2.21.0-IGB-gcc-4.9.4<br>2.26.0-IGB-gcc-4.9.4
|MPICH v3.x is an open source high-performance MPI 3.0 implementation.It does not support InfiniBand (use MVAPICH2 with InfiniBand devices).
+
|The BEDTools utilities allow one to address common genomics tasks such as finding feature overlaps and computing coverage. The utilities are largely based on four widely-used file formats: BED, GFF/GTF, VCF, and SAM/BAM. - Homepage: https://github.com/arq5x/bedtools2
 
|-
 
|-
|[https://github.com/mitoNGS/MToolBox MToolBox]
+
|[https://github.com/mgbellemare/Arcade-Learning-Environment ArcadeLearningEnvironment]
|1.0-IGB-gcc-4.9.4
+
|0.5.1-IGB-gcc-4.9.4-Python-2.7.13
|MToolBox is a highly automated bioinformatics pipeline to reconstruct and analyze human mitochondrial DNA from high throughput sequencing data. MToolBox includes an updated computational strategy to assemble mitochondrial genomes from Whole Exome and/or Genome Sequencing (PMID: 22669646) and an improved fragment-classify tool (PMID:22139932) for haplogroup assignment, functional and prioritization analysis of mitochondrial variants. MToolBox provides pathogenicity scores, profiles of genome variability and disease-associations for mitochondrial variants. MToolBox provides also a Variant Call Format file (version 4.0) featuring, for the first time, allele-specific heteroplasmy.
+
|The Arcade Learning Environment (ALE) -- a platform for AI research. - Homepage: https://github.com/mgbellemare/Arcade-Learning-Environment
 
|-
 
|-
|[http://mummer.sourceforge.net/ MUMmer]
+
|[https://github.com/ncbi/ncbi-vdb ncbi-vdb]
|3.23-IGB-gcc-4.9.4<br>4.0.0beta2-IGB-gcc-4.9.4
+
|2.8.2-IGB-gcc-4.9.4
|MUMmer is a system for rapidly aligning entire genomes, whether in complete or draft form. AMOS makes use of it.
+
|The SRA Toolkit and SDK from NCBI is a collection of tools and libraries for using data in the INSDC Sequence Read Archives. - Homepage: https://github.com/ncbi/ncbi-vdb
 
|-
 
|-
|[http://drive5.com/muscle/ MUSCLE]
+
|[https://developer.gnome.org/gdk-pixbuf/stable/ Gdk-Pixbuf]
|3.8.31-IGB-gcc-4.9.4
+
|.2.36.6-IGB-gcc-4.9.4-Python-2.7.13<br>.2.36.6-IGB-gcc-4.9.4-Python-3.6.1
|MUSCLE is one of the best-performing multiple alignment programs  according to published benchmark tests, with accuracy and speed that are consistently  better than CLUSTALW. MUSCLE can align hundreds of sequences in seconds. Most users  learn everything they need to know about MUSCLE in a few minutes—only a handful of  command-line options are needed to perform common alignment tasks. - Homepage: http://drive5.com/muscle/
+
|The Gdk Pixbuf is a toolkit for image loading and pixel buffer manipulation. It is used by GTK+ 2 and GTK+ 3 to load and manipulate images. In the past it was distributed as part of GTK+ 2 but it was split off into a separate package in preparation for the change to GTK+ 3.
 
|-
 
|-
|[http://www.genome.umd.edu/masurca.html MaSuRCA]
+
|[http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/ Trim_Galore]
|3.2.3-IGB-gcc-4.9.4
+
|0.4.4-IGB-gcc-4.9.4
|MaSuRCA is whole genome assembly software. It combines the efficiency of the de Bruijn graph  and Overlap-Layout-Consensus (OLC) approaches. MaSuRCA can assemble data sets containing  only short reads from Illumina sequencing or a mixture of short reads and long reads  (Sanger, 454, Pacbio and Nanopore).
+
|A wrapper tool around Cutadapt and FastQC to consistently apply  quality and adapter trimming to FastQ files, with some extra functionality for  MspI-digested RRBS-type (Reduced Representation Bisufite-Seq) libraries. - Homepage: http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/
 
|-
 
|-
|[http://www.makotemplates.org Mako]
+
|[https://github.com/ekg/freebayes FreeBayes]
|1.0.6-IGB-gcc-4.9.4-Python-3.6.1
+
|1.1.0-IGB-gcc-4.9.4
|A super-fast templating language that borrows the best ideas from the existing templating languages
+
|FreeBayes is a Bayesian genetic variant detector designed to find small polymorphisms, specifically SNPs (single-nucleotide polymorphisms), indels (insertions and deletions), MNPs (multi-nucleotide polymorphisms), and complex events (composite insertion and substitution events) smaller than the length of a short-read sequencing alignment.
 
|-
 
|-
|[http://www.netlab.uky.edu/p/bioinfo/MapSplice2 MapSplice]
+
|[https://github.com/hyattpd/prodigal Prodigal]
|2.2.1-IGB-gcc-4.9.4-Python-2.7.13
+
|2.6.3
|MapSplice is a software for mapping RNA-seq data to reference genome for splice junction discovery that depends only on reference genome, and not on any further annotations.
+
|Fast, reliable protein-coding gene prediction for prokaryotic genomes.
 
|-
 
|-
|[https://mariadb.org/ MariaDB]
+
|[http://zlib.net/pigz/ pigz]
|10.1.31-IGB-gcc-4.9.4<br>5.5.58-IGB-gcc-4.9.4
+
|2.3.4-IGB-gcc-4.9.4
|MariaDB An enhanced, drop-in replacement for MySQL.
+
|pigz, which stands for parallel implementation of gzip, is a fully  functional replacement for gzip that exploits multiple processors and multiple cores  to the hilt when compressing data. pigz was written by Mark Adler, and uses the zlib  and pthread libraries.  - Homepage: http://zlib.net/pigz/
 
|-
 
|-
|[https://bitbucket.org/berkeleylab/metabat MetaBAT]
+
|[http://www.htslib.org/ HTSlib]
|2.12.1
+
|1.3.1-IGB-gcc-4.9.4<br>1.4-IGB-gcc-4.9.4<br>1.5-IGB-gcc-4.9.4
|MetaBAT, an efficient tool for accurately reconstructing single genomes from complex microbial communities
+
|A C library for reading/writing high-throughput sequencing data. This package includes the utilities bgzip and tabix
 
|-
 
|-
|[http://metagene.nig.ac.jp/ MetaGeneAnnotator]
+
|[https://github.com/MikkelSchubert/adapterremoval AdapterRemoval]
|20080819-x86-64
+
|2.1.7-IGB-gcc-4.9.4
|MetaGeneAnnotator is a gene-finding program for prokaryote and phage.
+
|This program searches for and removes remnant adapter sequences from High-Throughput Sequencing (HTS) data and (optionally) trims low quality bases from the 3 end of reads following adapter removal.  
 
|-
 
|-
|[http://www.mothur.org/ Mothur]
+
|[http://sourceware.org/libffi/ libffi]
|1.38.1.1<br>1.39.5<br>1.39.5-IGB-gcc-4.9.4
+
|.3.2.1-IGB-gcc-4.9.4
|Mothur is a single piece of open-source, expandable software to fill the bioinformatics needs of the microbial ecology community.
+
|The libffi library provides a portable, high level programming interface to various callingconventions. This allows a programmer to call any function specified by a call interface description at run-time. - Homepage: http://sourceware.org/libffi/
 
|-
 
|-
|[http://multiqc.info/ MultiQC]
+
|[http://rpy.sourceforge.net/ rpy]
|0.9-IGB-gcc-4.9.4-Python-2.7.13<br>1.2-IGB-gcc-4.9.4-Python-2.7.13<br>1.2-IGB-gcc-4.9.4-Python-3.6.1
+
|1.0.3-IGB-gcc-4.9.4-Python-2.7.13-R-2.15.3
|MultiQC searches a given directory for analysis logs and compiles a HTML report. Its a general use tool, perfect for summarising the output from numerous bioinformatics tools.
+
|RPy is a very simple, yet robust, Python interface to the R Programming Language. Itcan manage all kinds of R objects and can execute arbitrary R functionsincluding the graphic functions.
 
|-
 
|-
|[http://www.nasm.us/ NASM]
+
|[https://github.com/matthiasplappert/keras-rl keras-rl]
|.2.12.02-IGB-gcc-4.9.4<br>2.12.02-IGB-gcc-4.9.4
+
|0.3.0-IGB-gcc-4.9.4-Python-2.7.13
|NASM: General-purpose x86 assembler
+
|keras-rl implements some state-of-the art deep reinforcement learning algorithms in Python and seamlessly integrates with the deep learning library Keras.  
 
|-
 
|-
|[http://nco.sourceforge.net NCO]
+
|[https://github.com/mahulchak/quickmerge quickmerge]
|4.7.2-IGB-gcc-4.9.4
+
|0.2-IGB-gcc-4.9.4-Python-2.7.13
|manipulates and analyzes data stored in netCDF-accessible formats, including DAP, HDF4, and HDF5
+
|quickmerge uses a simple concept to improve contiguity of genome assemblies based on long molecule sequences, often with dramatic outcomes. The program uses information from assemblies made with illumina short reads and PacBio long reads to improve contiguities of an assembly generated with PacBio long reads alone. This is counterintuitive because illumina short reads are not typically considered to cover genomic regions which PacBio long reads cannot. Although we have not evaluated this program for assemblies generated with Oxford nanopore sequences, the program should work with ONP-assemblies too.
 
|-
 
|-
|[https://github.com/ncbi/ngs NGS]
+
|[http://younglab.wi.mit.edu/super_enhancer_code.html ROSE]
|1.3.0-IGB-gcc-4.9.4
+
|20150210-IGB-gcc-4.9.4-Python-2.7.13
|NGS is a new, domain-specific API for accessing reads, alignments and pileups produced from Next Generation Sequencing. - Homepage: https://github.com/ncbi/ngs
+
|To create stitched enhancers, and to separate super-enhancers from typical enhancers using sequencing data (.bam)
 
|-
 
|-
|[http://www.nwchem-sw.org NWChem]
+
|[http://www.swig.org/ SWIG]
|6.6.revision27746-IGB-gcc-4.9.4-Python-2.7.13
+
|2.0.12-IGB-gcc-4.9.4-Python-2.7.13<br>3.0.12-IGB-gcc-4.9.4-Python-2.7.13<br>3.0.12-IGB-gcc-4.9.4-Python-2.7.13-Perl-5.24.1
|NWChem aims to provide its users with computational chemistry tools that are scalable both in their ability to treat large scientific computational chemistry problems efficiently, and in their use of available parallel computing resources from high-performance parallel supercomputers to conventional workstation clusters. NWChem software can handle: biomolecules, nanostructures, and solid-state; from quantum to classical, and all combinations; Gaussian basis functions or plane-waves; scaling from one to thousands of processors; properties and relativity.
+
|SWIG is a software development tool that connects programs written in C and C++ with a variety of high-level programming languages. - Homepage: http://www.swig.org/
 
|-
 
|-
|[https://ccl.northwestern.edu/netlogo/ NetLogo]
+
|[http://numba.pydata.org/ numba]
|5.2.1<br>6.0.3
+
|0.34.0-IGB-gcc-4.9.4-Python-2.7.13<br>0.34.0-IGB-gcc-4.9.4-Python-3.6.1
|NetLogo is a multi-agent programmable modeling environment. It is used by many tens of thousands of students, teachers and researchers worldwide.
+
|Numba is an Open Source NumPy-aware optimizing compiler for Python sponsored by Continuum Analytics, Inc. It uses the remarkable LLVM compiler infrastructure to compile Python syntax to machine code.
 
|-
 
|-
|[http://nucleoatac.readthedocs.io/en/latest/ NucleoATAC]
+
|[http://huttenhower.sph.harvard.edu/humann2 HUMAnN2]
|0.3.4-IGB-gcc-4.9.4-Python-2.7.13
+
|0.11.1-IGB-gcc-4.9.4-Python-3.6.1
|NucleoATAC is a python package for calling nucleosome positions and occupancy using ATAC-Seq data. Functions for calling nucleosomes are included in the nucleoatac command-line function. NucleoATAC also includes other utlities for working with ATAC-seq data under the pyatac function.
+
|HUMAnN is a pipeline for efficiently and accurately profiling the presence/absence and abundance of microbial pathways in a community from metagenomic or metatranscriptomic sequencing data (typically millions of short DNA/RNA reads). This process, referred to as functional profiling, aims to describe the metabolic potential of a microbial community and its members. More generally, functional profiling answers the question "What are the microbes in my community-of-interest doing (or capable of doing)?"
 
|-
 
|-
|[http://ocaml.org/ OCaml]
+
|[GNU binary utilities - Homepage: http://directory.fsf.org/project/binutils/ binutils]
|4.05.0-IGB-gcc-4.9.4
+
|.2.28<br>.2.28-GCCcore-4.9.4
|OCaml is a general purpose industrial-strength programming language with an emphasis on expressiveness and safety. Developed for more than 20 years at Inria it benefits from one of the most advanced type systems and supports functional, imperative and object-oriented styles of programming.
+
|binutils: GNU binary utilities - Homepage: http://directory.fsf.org/project/binutils/
 
|-
 
|-
|[http://xianyi.github.com/OpenBLAS/ OpenBLAS]
+
|[http://sourceforge.net/projects/junit JUnit]
|.0.2.19-GCC-4.9.4-2.28-LAPACK-3.7.0<br>0.2.19-GCC-4.9.4-2.28-LAPACK-3.7.0
+
|4.12-Java-1.8.0_121
|OpenBLAS is an optimized BLAS library based on GotoBLAS2 1.13 BSD version. - Homepage: http://xianyi.github.com/OpenBLAS/
+
|A programmer-oriented testing framework for Java.
 
|-
 
|-
|[http://opencv.org/ OpenCV]
+
|[http://www.fftw.org FFTW]
|3.1.0-IGB-gcc-4.9.4-Python-2.7.13<br>3.3.0-IGB-gcc-4.9.4-Python-3.6.1
+
|.3.3.6-gompi-4.9.4
|OpenCV (Open Source Computer Vision Library) is an open source computer vision and machine learning software library. OpenCV was built to provide a common infrastructure for computer vision applications and to accelerate the use of machine perception in the commercial products.
+
|FFTW is a C subroutine library for computing the discrete Fourier transform (DFT) in one or more dimensions, of arbitrary input size, and of both real and complex data. - Homepage: http://www.fftw.org
 
|-
 
|-
|[http://www.open-mpi.org/ OpenMPI]
+
|[https://ccb.jhu.edu/software/kraken/ Kraken]
|2.1.0-GCC-4.9.4-2.28
+
|1.0-IGB-gcc-4.9.4
|The Open MPI Project is an open source MPI-2 implementation.
+
|Kraken is a system for assigning taxonomic labels to short DNA sequences, usually obtained through metagenomic studies. Previous attempts by other bioinformatics software to accomplish this task have often used sequence alignment or machine learning techniques that were quite slow, leading to the development of less sensitive but much faster abundance estimation programs.  
 
|-
 
|-
|[http://code.google.com/p/openpgm/ OpenPGM]
+
|[http://mafft.cbrc.jp/alignment/software/ MAFFT]
|5.2.122-IGB-gcc-4.9.4
+
|7.310-IGB-gcc-4.9.4
|OpenPGM is an open source implementation of the Pragmatic General Multicast (PGM) specification in RFC 3208 available at www.ietf.org. PGM is a reliable and scalable multicast protocol that enables receivers to detect loss, request retransmission of lost data, or notify an application of unrecoverable loss. PGM is a receiver-reliable protocol, which means the receiver is responsible for ensuring all data is received, absolving the sender of reception responsibility.
+
|MAFFT is a multiple sequence alignment program  for unix-like operating systems.  It offers a range of multiple alignment methods, L-INS-i (accurate; for alignment of <∼200 sequences), FFT-NS-2 (fast; for alignment of <∼10,000 sequences), etc. - Homepage: http://mafft.cbrc.jp/alignment/software/
 
|-
 
|-
|[http://orthomcl.org/ OrthoMCL]
+
|[http://www.bioinformatics.babraham.ac.uk/projects/fastqc/ FastQC]
|2.0.9-IGB-gcc-4.9.4-Perl-5.24.1
+
|0.11.5-IGB-gcc-4.9.4-Java-1.8.0_121<br>0.11.5-IGB-gcc-4.9.4-Java-1.8.0_152
|OrthoMCL is a genome-scale algorithm for grouping orthologous protein sequences. - Homepage: http://orthomcl.org/
+
|FastQC is a quality control application for high throughput sequence data. It reads in sequence data in a variety of formats and can either provide an interactive application to review the results of several different QC checks, or create an HTML based report which can be integrated into a pipeline.
 
|-
 
|-
|[http://wasabiapp.org/software/pagan PAGAN]
+
|[http://matsen.fhcrc.org/pplacer/ pplacer]
|20150723-IGB-gcc-4.9.4
+
|1.1.alpha19
|PAGAN is a general-purpose method for the alignment of sequence graphs. PAGAN is based on the phylogeny-aware progressive alignment algorithm and uses graphs to describe the uncertainty in the presence of characters at certain sequence positions. However, graphs also allow describing the uncertainty in input sequences and modelling e.g. homopolymer errors in Roche 454 reads, or representing inferred ancestral sequences against which other sequences can then be aligned. PAGAN is still under development and will hopefully evolve to an easy-to-use, general-purpose method for phylogenetic sequence alignment.
+
|Pplacer places query sequences on a fixed reference phylogenetic tree to maximize phylogenetic likelihood or posterior probability according to a reference alignment. Pplacer is designed to be fast, to give useful information about uncertainty, and to offer advanced visualization and downstream analysis.
 
|-
 
|-
|[http://abacus.gene.ucl.ac.uk/software/paml.html PAML]
+
|[https://github.com/bcgsc/arcs ARCS]
|4.9e-IGB-gcc-4.9.4
+
|1.0.0-IGB-gcc-4.9.4-Perl-5.24.1
|PAML is a package of programs for phylogenetic  analyses of DNA or protein sequences using maximum likelihood. - Homepage: http://abacus.gene.ucl.ac.uk/software/paml.html
+
|Scaffolding genome sequence assemblies using 10X Genomics GemCode/Chromium data. - Homepage: https://github.com/bcgsc/arcs
 
|-
 
|-
|[https://github.com/neufeld/pandaseq PANDAseq]
+
|[http://www.zeromq.org/ ZeroMQ]
|2.11-IGB-gcc-4.9.4
+
|4.2.2-IGB-gcc-4.9.4
|PANDAseq assembles Illumina Solexa overlapping pair-end reads. - Homepage: https://github.com/neufeld/pandaseq
+
|ZeroMQ looks like an embeddable networking library but acts like a concurrency framework. It gives you sockets that carry atomic messages across various transports like in-process, inter-process, TCP, and multicast. You can connect sockets N-to-N with patterns like fanout, pub-sub, task distribution, and request-reply. It is fast enough to be the fabric for clustered products. Its asynchronous I/O model gives you scalable multicore applications, built as asynchronous message-processing tasks. It has a score of language APIs and runs on most operating systems.
 
|-
 
|-
|[http://www.pcre.org/ PCRE]
+
|[http://trac.osgeo.org/proj/ PROJ]
|.8.40-IGB-gcc-4.9.4
+
|.4.9.3-IGB-gcc-4.9.4
|The PCRE library is a set of functions that implement regular expression pattern matching using the same syntax and semantics as Perl 5. - Homepage: http://www.pcre.org/
+
|Program proj is a standard Unix filter function which converts geographic longitude and latitude coordinates into cartesian coordinates - Homepage: http://trac.osgeo.org/proj/
 
|-
 
|-
|[http://sco.h-its.org/exelixis/web/software/pear/ PEAR]
+
|[http://freetype.org freetype]
|0.9.8-IGB-gcc-4.9.4
+
|2.7.1-IGB-gcc-4.9.4
|PEAR is an ultrafast, memory-efficient and highly accurate pair-end read merger. It is fully parallelized and can run with as low as just a few kilobytes of memory. - Homepage: http://sco.h-its.org/exelixis/web/software/pear/
+
|FreeType 2 is a software font engine that is designed to be small, efficient, highly customizable, and portable while capable of producing high-quality output (glyph images). It can be used in graphics libraries, display servers, font conversion tools, text image generation tools, and many other products as well. - Homepage: http://freetype.org
 
|-
 
|-
|[http://picrust.github.io/picrust/ PICRUSt]
+
|[http://asperasoft.com/ aspera]
|1.1.1-IGB-gcc-4.9.4-Python-2.7.13<br>1.1.3-IGB-gcc-4.9.4-Python-2.7.13
+
|3.7.6
|PICRUSt (pronounced pie crust) is a bioinformatics software package designed to predict metagenome functional content from marker gene (e.g., 16S rRNA) surveys and full genomes.
+
|Aspera’s unwavering mission is to create the next-generation software technologies that move the world’s data at maximum speed, regardless of file size, transfer distance and network conditions.
 
|-
 
|-
|[https://genie.weizmann.ac.il/pubs/mir07/mir07_exe.html PITA]
+
|[http://apps.jcns.fz-juelich.de/doku/sc/libcerf libcerf]
|6-IGB-gcc-4.9.4
+
|1.5-IGB-gcc-4.9.4
|The PITA executable allows you to identify and score microRNA targets on UTRs.
+
|libcerf is a self-contained numeric library that provides an efficient and accurate implementation of complex error functions, along with Dawson, Faddeeva, and Voigt functions. - Homepage: http://apps.jcns.fz-juelich.de/doku/sc/libcerf
 
|-
 
|-
|[http://wasabiapp.org/software/prank/ PRANK]
+
|[https://developer.gnome.org/ATK/stable/ ATK]
|170427-IGB-gcc-4.9.4
+
|.2.24.0-IGB-gcc-4.9.4-Python-2.7.13<br>.2.24.0-IGB-gcc-4.9.4-Python-3.6.1
|PRANK is a probabilistic multiple alignment program for DNA, codon and amino-acid sequences. It’s based on a novel algorithm that treats insertions correctly and avoids over-estimation of the number of deletion events. In addition, PRANK borrows ideas from maximum likelihood methods used in phylogenetics and correctly takes into account the evolutionary distances between sequences. Lastly, PRANK allows for defining a potential structure for sequences to be aligned and then, simultaneously with the alignment, predicts the locations of structural units in the sequences.
+
|ATK provides the set of accessibility interfaces that are implemented by other toolkits and applications. Using the ATK interfaces, accessibility tools have full access to view and control running applications.
 
|-
 
|-
|[http://trac.osgeo.org/proj/ PROJ]
+
|[https://github.com/lh3/seqtk/ seqtk]
|.4.9.3-IGB-gcc-4.9.4
+
|1.2-IGB-gcc-4.9.4
|Program proj is a standard Unix filter function which converts geographic longitude and latitude coordinates into cartesian coordinates - Homepage: http://trac.osgeo.org/proj/
+
|Seqtk is a fast and lightweight tool for processing sequences in the FASTA or FASTQ format.  It seamlessly parses both FASTA and FASTQ files which can also be optionally compressed by gzip. - Homepage: https://github.com/lh3/seqtk/
 
|-
 
|-
|[http://www.pango.org/ Pango]
+
|[https://github.com/marbl/canu Canu]
|.1.40.6-IGB-gcc-4.9.4
+
|1.4-IGB-gcc-4.9.4-Perl-5.24.1<br>1.5-IGB-gcc-4.9.4-Perl-5.24.1<br>1.6-IGB-gcc-4.9.4-Perl-5.24.1<br>1.7-IGB-gcc-4.9.4-Perl-5.24.1<br>1.7.1-IGB-gcc-4.9.4-Perl-5.24.1
|Pango is a library for laying out and rendering of text, with an emphasis on internationalization.Pango can be used anywhere that text layout is needed, though most of the work on Pango so far has been done in thecontext of the GTK+ widget toolkit. Pango forms the core of text and font handling for GTK+-2.x. - Homepage: http://www.pango.org/
+
|Canu is a fork of the Celera Assembler, designed for high-noise single-molecule sequencing (such as the PacBio RS II or Oxford Nanopore MinION).
 
|-
 
|-
|[https://github.com/shawnzhangyx/PePr PePr]
+
|[https://daler.github.io/pybedtools/main.html pybedtools]
|1.1.21-IGB-gcc-4.9.4-Python-2.7.13
+
|0.7.10-IGB-gcc-4.9.4-Python-3.6.1
|PePr is a ChIP-Seq Peak-calling and Prioritization pipeline that uses a sliding window approach and models read counts across replicates and between groups with a negative binomial distribution.
+
|pybedtools is a Python package that wraps BEDTools, so you will need both installed.
 
|-
 
|-
|[http://www.perl.org/ Perl]
+
|[http://cgit.freedesktop.org/xorg/lib/libpciaccess/ libpciaccess]
|5.24.1-IGB-gcc-4.9.4<br>5.24.1-IGB-gcc-4.9.4-bare<br>5.26.1-IGB-gcc-4.9.4-unthreaded
+
|.0.13.4-IGB-gcc-4.9.4
|Larry Wall Practical Extraction and Report Language
+
|Generic PCI access library.
 
|-
 
|-
|[https://github.com/kundajelab/phantompeakqualtools Phantompeaktools]
+
|[https://www.continuum.io/anaconda-overview Anaconda2]
|1.2-IGB-gcc-4.9.4-R-3.4.1
+
|4.3.1
|Custom SPP for Phantompeaktools
+
|Built to complement the rich, open source Python community,the Anaconda platform provides an enterprise-ready data analytics platform that empowers companies to adopt a modern open data science analytics architecture. - Homepage: https://www.continuum.io/anaconda-overview
 
|-
 
|-
|[https://github.com/kundajelab/phantompeakqualtools Phantompeaktools-spp]
+
|[http://http://sox.sourceforge.net/ SoX]
|.1.2-IGB-gcc-4.9.4-R-3.4.1
+
|14.4.2-IGB-gcc-4.9.4
|Custom SPP for Phantompeaktools
+
|Sound eXchange, the Swiss Army knife of audio manipulation
 
|-
 
|-
|[https://sourceforge.net/projects/phispy PhiSpy]
+
|[http://vfsmspineagent.fsm.northwestern.edu/ Spine]
|2.3-IGB-gcc-4.9.4-Python-2.7.13
+
|0.2.1-IGB-gcc-4.9.4
|A novel algorithm for finding prophages in microbial genomes that combines similarity-based and composition-based strategies
+
|Spine identifies a core genome from input genomic sequences. Sequences are aligned using Nucmer and regions found to be in common between all or a user-defined subset of genomes will be returned.
 
|-
 
|-
|[http://pillow.readthedocs.org/ Pillow]
+
|[http://guidance.tau.ac.il/ver2/ GUIDANCE]
|5.1.0-IGB-gcc-4.9.4-Python-2.7.13<br>5.1.0-IGB-gcc-4.9.4-Python-3.6.1
+
|2.02-IGB-gcc-4.9.4-Perl-5.24.1
|Pillow is the friendly PIL fork by Alex Clark and Contributors. PIL is the Python Imaging Library by Fredrik Lundh and Contributors.
+
|GUIDANCE is meant to be used for weighting, filtering or masking unreliably aligned positions in sequence alignments before subsequent analysis. For example, align codon sequences (nucleotide sequences that code for proteins) using PAGAN, remove columns with low GUIDANCE scores, and use the remaining alignment to infer positive selection using the branch-site dN/dS test. Other analyses where GUIDANCE filtering could be useful include phylogeny reconstruction, reconstruction of the history of specific insertion and deletion events, inference of recombination events, etc. - Homepage: http://guidance.tau.ac.il/ver2/
 
|-
 
|-
|[https://github.com/rrwick/Porechop Porechop]
+
|[http://www.oberhumer.com/opensource/lzo/ lzo]
|0.2.3-IGB-gcc-4.9.4-Python-3.6.1
+
|.2.10-IGB-gcc-4.9.4
|Porechop is a tool for finding and removing adapters from Oxford Nanopore reads.
+
|Portable lossless data compression library
 
|-
 
|-
|[https://github.com/hyattpd/prodigal Prodigal]
+
|[http://www.gnu.org/software/coreutils/coreutils.html coreutils]
|2.6.3
+
|8.28-IGB-gcc-4.9.4
|Fast, reliable protein-coding gene prediction for prokaryotic genomes.
+
|The GNU Core Utilities are the basic file, shell and text manipulation utilities of the GNU operating system.These are the core utilities which are expected to exist on every operating system.  
 
|-
 
|-
|[https://github.com/uoregon-postlethwait/prost Prost]
+
|[http://soap.genomics.org.cn/SOAPdenovo-Trans.html SOAPdenovo-Trans]
|0.7.45-IGB-gcc-4.9.4-Python-2.7.13
+
|1.03
|Prost (PRocessing Of Small Transcripts) is a python application that quantifies and annotates microRNA (miRNA) expression in metazoans with assembled genomes. Prost works by counting short transcripts within a user-specifiable length range. These counted transcripts are aligned to a user specifiable genome allowing for post-transcriptional modification (e.g. untemplated additions, editing, alternative cutting) and then "binned" together based on genomic location. Each bin is then annotated with databases of mature miRNAs, hairpins, and other types of RNAs (the databases may be derived from miRBase, Ensembls BioMart, other databases, or may be custom built by the user).
+
|SOAPdenovo-Trans is a de novo transcriptome assembler basing on the SOAPdenovo framework, adapt to alternative splicing and different expression level among transcripts.The assembler provides a more accurate, complete and faster way to construct the full-length transcript sets.  
 
|-
 
|-
|[https://mathema.tician.de/software/pycuda/ PyCUDA]
+
|[http://deeplearning.net/software/theano Theano]
|2017.1-IGB-gcc-4.9.4-Python-2.7.13
+
|0.9.0-IGB-gcc-4.9.4-Python-2.7.13
|PyCUDA lets you access Nvidia‘s CUDA parallel computation API from Python. - Homepage: https://mathema.tician.de/software/pycuda/
+
|Theano is a Python library that allows you to define, optimize,and evaluate mathematical expressions involving multi-dimensional arrays efficiently. - Homepage: http://deeplearning.net/software/theano
 
|-
 
|-
|[http://pytorch.org PyTorch]
+
|[https://github.com/jts/nanopolish nanopolish]
|0.3.0-IGB-gcc-4.9.4-Python-3.6.1<br>0.4.0-IGB-gcc-4.9.4-Python-3.6.1
+
|0.10.1-IGB-gcc-4.9.4<br>0.6.0-IGB-gcc-4.9.4<br>0.7.1-IGB-gcc-4.9.4<br>0.7.1-IGB-gcc-4.9.4-159d92b<br>0.8.3-IGB-gcc-4.9.4<br>0.8.5-IGB-gcc-4.9.4<br>0.9.0-IGB-gcc-4.9.4
|Tensors and Dynamic neural networks in Pythonwith strong GPU acceleration.
+
|Software package for signal-level analysis of Oxford Nanopore sequencing data.
 
|-
 
|-
|[http://www.zeromq.org/bindings:python PyZMQ]
+
|[http://www.unidata.ucar.edu/software/netcdf/ netCDF-Fortran]
|16.0.2-IGB-gcc-4.9.4-Python-3.6.1
+
|.4.4.1-IGB-gcc-4.9.4<br>4.4.1-IGB-gcc-4.9.4
|Python bindings for ZeroMQ
+
|NetCDF (network Common Data Form) is a set of software libraries and machine-independent data formats that support the creation, access, and sharing of array-oriented scientific data.
 
|-
 
|-
|[https://github.com/pysam-developers/pysam Pysam]
+
|[http://www.htslib.org/ BCFtools]
|0.13.0-IGB-gcc-4.9.4-Python-2.7.13<br>0.13.0-IGB-gcc-4.9.4-Python-3.6.1
+
|1.4-IGB-gcc-4.9.4<br>1.5-IGB-gcc-4.9.4<br>1.7-IGB-gcc-4.9.4
|Pysam is a python module for reading and manipulating Samfiles.  Its a lightweight wrapper of the samtools C-API. Pysam also includes an interface for tabix.
+
|BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF
 
|-
 
|-
|[http://python.org/ Python]
+
|[https://github.com/biocore-ntnu/epic epic]
|2.7.13-IGB-gcc-4.9.4<br>3.6.1-IGB-gcc-4.9.4
+
|0.2.9-IGB-gcc-4.9.4-Python-2.7.13
|Python is a programming language that lets you work more quickly and integrate your systems more effectively.
+
|epic is a software package for finding medium to diffusely enriched domains in chip-seq data. It is a fast, parallel and memory-efficient implementation of the incredibly popular SICER algorithm.  
 
|-
 
|-
|[http://qiime.org/ QIIME]
+
|[http://java.com/ Java]
|1.9.1
+
|1.8.0_121<br>1.8.0_152
|QIIME is an open-source bioinformatics pipeline for performing microbiome analysis from raw DNA sequencing data.
+
|Java Platform, Standard Edition (Java SE) lets you develop and deploy Java applications on desktops and servers. - Homepage: http://java.com/
 
|-
 
|-
|[http://qiime.org/ QIIME2]
+
|[http://www.genome.umd.edu/jellyfish.html Jellyfish]
|2017.10<br>2017.11<br>2017.12<br>2017.6<br>2017.8<br>2018.2<br>2018.4<br>2018.6
+
|1.1.12-IGB-gcc-4.9.4<br>2.2.6-IGB-gcc-4.9.4
|QIIME is an open-source bioinformatics pipeline for performing microbiome analysis from raw DNA sequencing data.
+
|Jellyfish is a tool for fast, memory-efficient counting of k-mers in DNA. - Homepage: http://www.genome.umd.edu/jellyfish.html
 
|-
 
|-
|[http://qt.io/ Qt]
+
|[https://github.com/arq5x/poretools poretools]
|4.8.7-IGB-gcc-4.9.4
+
|0.6.0-IGB-gcc-4.9.4-Python-2.7.13
|Qt is a comprehensive cross-platform C++ application framework.
+
|a toolkit for working with nanopore sequencing data from Oxford Nanopore. - Homepage: https://github.com/arq5x/poretools
 
|-
 
|-
|[http://www.r-project.org/ R]
+
|[http://bioinform.github.io/breakseq2/ BreakSeq2]
|2.15.3-IGB-gcc-4.9.4<br>3.1.2-IGB-gcc-4.9.4<br>3.2.5-IGB-gcc-4.9.4<br>3.3.3-IGB-gcc-4.9.4<br>3.4.1-IGB-gcc-4.9.4<br>3.4.2-IGB-gcc-4.9.4<br>3.5.0-IGB-gcc-4.9.4
+
|2.2-IGB-gcc-4.9.4-Python-2.7.13
|R is a free software environment for statistical computing and graphics.
+
|Ultrafast and accurate nucleotide-resolution analysis of structural variants - Homepage: http://bioinform.github.io/breakseq2/
 
|-
 
|-
|[https://sourceforge.net/projects/rdp-classifier RDPClassifier]
+
|[https://bitbucket.org/biobakery/metaphlan2 metaphlan2]
|2.12-Java-1.8.0_152<br>2.2-Java-1.8.0_152
+
|2.6.0-IGB-gcc-4.9.4-Python-3.6.1<br>2.7.6-IGB-gcc-4.9.4-Python-2.7.13
|The RDP Classifier is a naive Bayesian classifier which was developed to provide rapid taxonomic placement based on rRNA sequence data. The RDP Classifier can rapidly and accurately classify bacterial and archaeal 16s rRNA sequences, and Fungal LSU sequences. It provides taxonomic assignments from domain to genus, with confidence estimates for each assignment.
+
|MetaPhlAn is a computational tool for profiling the composition of microbial communities (Bacteria, Archaea, Eukaryotes and Viruses) from metagenomic shotgun sequencing data (i.e. not 16S) with species-level. With the newly added StrainPhlAn module, it is now possible to perform accurate strain-level microbial profiling.
 
|-
 
|-
|[http://www.sanger.ac.uk/science/tools/reapr REAPR]
+
|[http://www.freedesktop.org/software/fontconfig fontconfig]
|1.0.18-IGB-gcc-4.9.4
+
|2.12.1-IGB-gcc-4.9.4
|REAPR is a tool that evaluates the accuracy of a genome assembly using mapped paired end reads, without the use of a reference genome for comparison. It can be used in any stage of an assembly pipeline to automatically break incorrect scaffolds and flag other errors in an assembly for manual inspection. It reports mis-assemblies and other warnings, and produces a new broken assembly based on the error calls. - Homepage: http://www.sanger.ac.uk/science/tools/reapr
+
|Fontconfig is a library designed to provide system-wide font configuration, customization andapplication access. - Homepage: http://www.freedesktop.org/software/fontconfig
 
|-
 
|-
|[http://www.regulatory-genomics.org/rgt/basic-introduction/ RGT]
+
|[http://bowtie-bio.sourceforge.net/index.shtml Bowtie]
|0.11.3-IGB-gcc-4.9.4-Python-2.7.13
+
|1.2.0-IGB-gcc-4.9.4
|Regulatory Genomics Toolbox (RGT) is an open source python library for analysis of regulatory genomics. RGT is programmed in an oriented object fashion and its core classes provide functionality for handling regulatory genomics data.  
+
|Bowtie is an ultrafast, memory-efficient short read aligner.It aligns short DNA sequences (reads) to the human genome. - Homepage: http://bowtie-bio.sourceforge.net/index.shtml
 
|-
 
|-
|[http://www.repeatmasker.org/RMBlast.html RMBlast]
+
|[https://www.tensorflow.org/ Tensorflow]
|2.6.0-IGB-gcc-4.9.4
+
|1.2.1-IGB-gcc-4.9.4-Python-2.7.13
|RMBlast is a RepeatMasker compatible version of the standard NCBI blastn program. The primary difference between this distribution and the NCBI distribution is the addition of a new program "rmblastn" for use with RepeatMasker and RepeatModeler.
+
|An open-source software library for Machine Intelligence
 
|-
 
|-
|[https://bibiserv2.cebitec.uni-bielefeld.de/rnahybrid RNAhybrid]
+
|[http://www.gnu.org/software/autoconf/ Autoconf]
|2.1.2-IGB-gcc-4.9.4
+
|.2.69<br>.2.69-IGB-gcc-4.9.4
|RNAhybrid is a tool for finding the minimum free energy hybridization of a long and a short RNA. The hybridization is performed in a kind of domain mode, ie. the short sequence is hybridized to the best fitting part of the long one. The tool is primarily meant as a means for microRNA target prediction.  
+
|Autoconf is an extensible package of M4 macros that produce shell scripts to automatically configure software source code packages. These scripts can adapt the packages to many kinds of UNIX-like systems without manual user intervention. Autoconf creates a configuration script for a package from a template file that lists the operating system features that the package can use, in the form of M4 macro calls. - Homepage: http://www.gnu.org/software/autoconf/
 
|-
 
|-
|[http://www.cbs.dtu.dk/cgi-bin/sw_request?rnammer RNAmmer]
+
|[http://www.microbesonline.org/fasttree/ FastTree]
|1.2-IGB-gcc-4.9.4-Perl-5.24.1
+
|2.1.10-IGB-gcc-4.9.4
|Ribosomal RNA sub units
+
|FastTree infers approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences. FastTree can handle alignments with up to a million of sequences in a reasonable amount of time and memory.  
 
|-
 
|-
|[http://rna.urmc.rochester.edu/RNAstructure.html RNAstructure]
+
|[https://github.com/adrianlopezroche/fdupes fdupes]
|6.0-IGB-gcc-4.9.4
+
|1.6.1-IGB-gcc-4.9.4
|RNAstructure is a complete package for RNA and DNA secondary structure prediction and analysis. It includes algorithms for secondary structure prediction, including facility to predict base pairing probabilities.  
+
|FDUPES is a program for identifying duplicate files residingwithin specified directories.
 
|-
 
|-
|[http://younglab.wi.mit.edu/super_enhancer_code.html ROSE]
+
|[http://www.cmake.org CMake]
|20150210-IGB-gcc-4.9.4-Python-2.7.13
+
|.3.12.1-IGB-gcc-4.9.4<br>.3.7.2-IGB-gcc-4.9.4
|To create stitched enhancers, and to separate super-enhancers from typical enhancers using sequencing data (.bam)
+
|CMake, the cross-platform, open-source build system. CMake is a family of tools designed to build, test and package software. - Homepage: http://www.cmake.org
 
|-
 
|-
|[http://deweylab.github.io/RSEM/ RSEM]
+
|[https://www.gnu.org/software/gperf/ gperf]
|1.3.0-IGB-gcc-4.9.4
+
|3.1-IGB-gcc-4.9.4
|RNA-Seq by Expectation-Maximization
+
|GNU gperf is a perfect hash function generator. For a given list of strings, it produces a hash function and hash table, in form of C or C++ code, for looking up a value depending on the input string. The hash function is perfect, which means that the hash table has no collisions, and the hash table lookup needs a single string comparison only.
 
|-
 
|-
|[http://rseqc.sourceforge.net/ RSeQC]
+
|[https://projects.coin-or.org/ADOL-C ADOL-C]
|2.6.4-IGB-gcc-4.9.4-Python-2.7.13
+
|2.6.3-IGB-gcc-4.9.4
|RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. Some basic modules quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while RNA-seq specific modules evaluate sequencing saturation, mapped reads distribution, coverage uniformity, strand specificity, transcript level RNA integrity etc.
+
|ADOL-C is an open-source package for the automatic differentiation of C and C++ programs.  
 
|-
 
|-
|[http://fenderglass.github.io/Ragout/ Ragout]
+
|[http://www.zlib.net/ zlib]
|2.0-IGB-gcc-4.9.4
+
|.1.2.11<br>.1.2.11-GCCcore-4.9.4<br>.1.2.11-IGB-gcc-4.9.4
|Ragout (Reference-Assisted Genome Ordering UTility) is a tool for chromosome assembly using multiple references.  
+
|zlib is designed to be a free, general-purpose, legally unencumbered -- that is, not covered by any patents -- lossless data-compression library for use on virtually any computer hardware and operating system. - Homepage: http://www.zlib.net/
 
|-
 
|-
|[https://cran.r-project.org/web/packages/RcppGSL/index.html RcppGSL]
+
|[https://genie.weizmann.ac.il/pubs/mir07/mir07_exe.html PITA]
|0.3.2-IGB-gcc-4.9.4-R-3.3.3
+
|6-IGB-gcc-4.9.4
|Rcpp integration for GNU GSL vectors and matrices The GNU Scientific Library (or GSL) is a collection of numerical routines for scientific computing. It is particularly useful for C and C++ programs as it provides a standard C interface to a wide range of mathematical routines. There are over 1000 functions in total with an extensive test suite. The RcppGSL package provides an easy-to-use interface between GSL data structures and R using concepts from Rcpp which is itself a package that eases the interfaces between R and C++. This package also serves as a prime example of how to build a package that uses Rcpp to connect to another third-party library. The autoconf script, inline plugin and example package can all be used as a stanza to write a similar package against another library.
+
|The PITA executable allows you to identify and score microRNA targets on UTRs.
 
|-
 
|-
|[http://www.repeatmasker.org/ RepeatMasker]
+
|[https://github.com/marbl/Krona Krona]
|4.0.7-IGB-gcc-4.9.4-Perl-5.24.1<br>4.0.7-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
+
|2.7-IGB-gcc-4.9.4-Perl-5.24.1
|RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences.  
+
|Interactively explore metagenomes and more from a web browser.
 
|-
 
|-
|[https://cran.r-project.org/web/packages/Rmpi/index.html Rmpi]
+
|[http://www.bork.embl.de/pal2nal/ pal2nal]
|0.6-6-IGB-gcc-4.9.4-R-3.4.2
+
|14-IGB-gcc-4.9.4
|An interface (wrapper) to MPI APIs. It also provides interactive R manager and worker environment.
+
|PAL2NAL is a program that converts a multiple sequence alignment of proteins and the corresponding DNA (or mRNA) sequences into a codon alignment.
 
|-
 
|-
|[https://www.ruby-lang.org Ruby]
+
|[https://github.com/rrwick/Unicycler Unicycler]
|2.4.2-IGB-gcc-4.9.4
+
|0.4.3-IGB-gcc-4.9.4-Python-3.6.1<br>0.4.4-IGB-gcc-4.9.4-Python-3.6.1
|Ruby is a dynamic, open source programming language with  a focus on simplicity and productivity. It has an elegant syntax that is  natural to read and easy to write.
+
|Unicycler is an assembly pipeline for bacterial genomes. It can assemble Illumina-only read sets where it functions as a SPAdes-optimiser. It can also assembly long-read-only sets (PacBio or Nanopore) where it runs a miniasm+Racon pipeline. For the best possible assemblies, give it both Illumina reads and long reads, and it will conduct a hybrid assembly.
 
|-
 
|-
|[http://www.htslib.org/ SAMtools]
+
|[http://homer.ucsd.edu/homer/ HOMER]
|0.1.20-IGB-gcc-4.9.4<br>1.4-IGB-gcc-4.9.4<br>1.4.1-IGB-gcc-4.9.4<br>1.5-IGB-gcc-4.9.4<br>1.7-IGB-gcc-4.9.4
+
|4.9.1-IGB-gcc-4.9.4-Perl-5.24.1
|SAM Tools provide various utilities for manipulating alignments in the SAM format,  including sorting, merging, indexing and generating alignments in a per-position format.
+
|HOMER (Hypergeometric Optimization of Motif EnRichment) is a suite of tools for Motif Discovery and ChIP-Seq analysis. It is a collection of command line programs for unix-style operating systems written in mostly perl and c++. Homer was primarily written as a de novo motif discovery algorithm that is well suited for finding 8-12 bp motifs in large scale genomics data.
 
|-
 
|-
|[http://www.scons.org/ SCons]
+
|[http://xianyi.github.com/OpenBLAS/ OpenBLAS]
|3.0.1-IGB-gcc-4.9.4-Python-2.7.13<br>3.0.1-IGB-gcc-4.9.4-Python-3.6.1
+
|.0.2.19-GCC-4.9.4-2.28-LAPACK-3.7.0<br>0.2.19-GCC-4.9.4-2.28-LAPACK-3.7.0
|SCons is a software construction tool.
+
|OpenBLAS is an optimized BLAS library based on GotoBLAS2 1.13 BSD version. - Homepage: http://xianyi.github.com/OpenBLAS/
 
|-
 
|-
|[http://www.libsdl.org/ SDL2]
+
|[http://www.well.ox.ac.uk/~cfreeman/software/gwas/gtool.html gtool]
|2.0.4-IGB-gcc-4.9.4
+
|0.7.5
|SDL: Simple DirectMedia Layer, a cross-platform multimedia library
+
|GTOOL is a program for transforming sets of genotype data for use with the programs SNPTEST and IMPUTE.
 
|-
 
|-
|[https://github.com/smirarab/sepp SEPP]
+
|[https://www.gnu.org/software/sharutils/ sharutils]
|20180223-IGB-gcc-4.9.4-Python-2.7.13
+
|4.15.2-IGB-gcc-4.9.4
|SEPP stands for "SATe-enabled Phylogenetic Placement", and addresses the problem of phylogenetic placement of short reads into reference alignments and trees.
+
|GNU shar makes so-called shell archives out of many files, preparing them for transmission by electronic mail services, while unshar helps unpacking shell archives after reception.
 
|-
 
|-
|[https://github.com/ruanjue/smartdenovo SMARTdenovo]
+
|[https://bitbucket.org/nsegata/graphlan/ graphlan]
|20170916-IGB-gcc-4.9.4-Perl-5.24.1
+
|6ca8735-IGB-gcc-4.9.4-Python-2.7.13
|SMARTdenovo is a de novo assembler for PacBio and Oxford Nanopore (ONT) data. It produces an assembly from all-vs-all raw read alignments without an error correction stage. It also provides tools to generate accurate consensus sequences, though a platform dependent consensus polish tools (e.g. Quiver for PacBio or Nanopolish for ONT) are still required for higher accuracy.
+
|GraPhlAn is a software tool for producing high-quality circular representations of taxonomic and phylogenetic trees. It focuses on concise, integrative, informative, and publication-ready representations of phylogenetically- and taxonomically-driven investigation.
 
|-
 
|-
|[http://korflab.ucdavis.edu/software.html SNAP]
+
|[http://www.broadinstitute.org/software/discovar/blog/ DISCOVARdenovo]
|2013-11-29-IGB-gcc-4.9.4
+
|52488-IGB-gcc-4.9.4
|(Semi-HMM-based Nucleic Acid Parser) gene prediction tool
+
|DISCOVAR de novo can generate de novo assemblies for both large and small genomes. It currently does not call variants.
 
|-
 
|-
|[http://snver.sourceforge.net/ SNVer]
+
|[http://www.gurobi.com/ Gurobi]
|0.5.3-Java-1.8.0_121
+
|7.5.2
|SNVer is a statistical tool for calling common and rare variants in analysis of pool or individual next-generation sequencing data. It reports one single overall p-value for evaluating the significance of a candidate locus being a variant, based on which multiplicity control can be obtained.  
+
|The Gurobi Optimizer was designed from the ground up to be the fastest, most powerful solver available for your LP, QP, QCP, and MIP (MILP, MIQP, and MIQCP) problems.
 
|-
 
|-
|[http://soap.genomics.org.cn/SOAPdenovo-Trans.html SOAPdenovo-Trans]
+
|[http://www.pixman.org/ pixman]
|1.03
+
|0.34.0-IGB-gcc-4.9.4
|SOAPdenovo-Trans is a de novo transcriptome assembler basing on the SOAPdenovo framework, adapt to alternative splicing and different expression level among transcripts.The assembler provides a more accurate, complete and faster way to construct the full-length transcript sets.  
+
|Pixman is a low-level software library for pixel manipulation, providing features such as imagecompositing and trapezoid rasterization. Important users of pixman are the cairo graphics library and the X server. - Homepage: http://www.pixman.org/
 
|-
 
|-
|[http://cab.spbu.ru/software/spades/ SPAdes]
+
|[https://www.tbi.univie.ac.at/RNA/ ViennaRNA]
|3.10.1-IGB-gcc-4.9.4-Python-2.7.13<br>3.11.0-IGB-gcc-4.9.4-Python-2.7.13<br>3.11.0-IGB-gcc-4.9.4-Python-3.6.1<br>3.11.1-IGB-gcc-4.9.4-Python-3.6.1
+
|2.4.2-IGB-gcc-4.9.4
|SPAdes . St. Petersburg genome assembler . is intended for both standard isolates and single-cell MDA bacteria assemblies.
+
|The ViennaRNA Package consists of a C code library and several stand-alone programs for the prediction and comparison of RNA secondary structures.  
 
|-
 
|-
|[http://www.sqlite.org/ SQLite]
+
|[https://github.com/PacificBiosciences/FALCON_unzip FALCON_unzip]
|3.17.0-IGB-gcc-4.9.4
+
|0.4.0-IGB-gcc-4.9.4-Python-2.7.13
|SQLite: SQL Database Engine in a C Library
+
|FALCON-Unzip contains the modules that works with FALCON for full diploid assembly (representing haplotype specific contigs as "haplotigs" as assembly output).
 
|-
 
|-
|[http://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=std SRA-Toolkit]
+
|[http://pb-falcon.readthedocs.io/en/latest/index.html FALCON]
|2.8.2-1
+
|1.8.8-IGB-gcc-4.9.4-Python-2.7.13
|The NCBI SRA Toolkit enables reading (dumping) of sequencing files from the SRA database and writing (loading) files into the .sra format  - Homepage: http://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=std
+
|FALCON is a diploid aware genome assembler designed for Pacific Biosciences long read data.
 
|-
 
|-
|[https://github.com/alexdobin/STAR STAR]
+
|[http://cgit.freedesktop.org/xorg/util/macros xorg-macros]
|2.5.3a-IGB-gcc-4.9.4<br>2.6.0c-IGB-gcc-4.9.4<br>2.6.1b-IGB-gcc-4.9.4
+
|.1.19.0-IGB-gcc-4.9.4
|STAR aligns RNA-seq reads to a reference genome using uncompressed suffix arrays.
+
|X.org macros utilities.
 
|-
 
|-
|[http://computation.llnl.gov/projects/sundials SUNDIALS]
+
|[https://github.com/nanoporetech/scrappie scrappie]
|2.6.2-IGB-gcc-4.9.4
+
|1.3.0-IGB-gcc-4.9.4
|SUNDIALS: SUite of Nonlinear and DIfferential/ALgebraic Equation Solvers
+
|Scrappie is a technology demonstrator for the Oxford Nanopore Research Algorithms group.
 
|-
 
|-
|[http://www.swig.org/ SWIG]
+
|[https://github.com/seqan/flexbar flexbar]
|2.0.12-IGB-gcc-4.9.4-Python-2.7.13<br>3.0.12-IGB-gcc-4.9.4-Python-2.7.13<br>3.0.12-IGB-gcc-4.9.4-Python-2.7.13-Perl-5.24.1
+
|3.0.3-IGB-gcc-4.9.4
|SWIG is a software development tool that connects programs written in C and C++ with a variety of high-level programming languages. - Homepage: http://www.swig.org/
+
|The program Flexbar preprocesses high-throughput sequencing data efficiently. It demultiplexes barcoded runs and removes adapter sequences. Moreover, trimming and filtering features are provided.  
 
|-
 
|-
|[https://github.com/COMBINE-lab/salmon Salmon]
+
|[http://www.imagemagick.org/ ImageMagick]
|0.11.3-IGB-gcc-4.9.4<br>0.8.2-IGB-gcc-4.9.4-Python-2.7.13<br>0.9.1-IGB-gcc-4.9.4
+
|7.0.5-5-IGB-gcc-4.9.4
|Salmon is a wicked-fast program to produce a highly-accurate, transcript-level quantification estimates from RNA-seq data.
+
|ImageMagick is a software suite to create, edit, compose, or convert bitmap images - Homepage: http://www.imagemagick.org/
 
|-
 
|-
|[http://www.netlib.org/scalapack/ ScaLAPACK]
+
|[https://www.nextflow.io/ nextflow]
|.2.0.2-gompi-4.9.4-OpenBLAS-0.2.19-LAPACK-3.7.0
+
|0.25.7-Java-1.8.0_121<br>0.26.3-Java-1.8.0_152
|The ScaLAPACK (or Scalable LAPACK) library includes a subset of LAPACK routines redesigned for distributed memory MIMD parallel computers. - Homepage: http://www.netlib.org/scalapack/
+
|Nextflow enables scalable and reproducible scientific workflows using software containers. It allows the adaptation of pipelines written in the most common scripting languages.  
 
|-
 
|-
|[https://www.pmgenomics.ca/hoffmanlab/proj/segway/ Segway]
+
|[http://vfsmspineagent.fsm.northwestern.edu/ AGEnt]
|2.0.1-IGB-gcc-4.9.4-Python-2.7.13
+
|0.2.1-IGB-gcc-4.9.4
|Segway is a tool for easy pattern discovery and identification in functional genomics data.
+
|AGEnt performs in silico subtractive hybridization of core genome sequences, such as those produced by Spine, against a query genomic sequence to identify accessory genomic sequences (AGEs) in the query genome. Sequences are aligned using Nucmer, outputting sequences and sequence characteristics of those regions in the query genome that are not found in the core genome. If gene coordinate information is provided, a list of accessory genes in the query genome will also be output.
 
|-
 
|-
|[https://github.com/bioinf/Sibelia Sibelia]
+
|[http://bowtie-bio.sourceforge.net/bowtie2/index.shtml Bowtie2]
|3.0.7-IGB-gcc-4.9.4
+
|2.1.0-IGB-gcc-4.9.4<br>2.3.1-IGB-gcc-4.9.4<br>2.3.2-IGB-gcc-4.9.4
|Sibelia is a tool for finding synteny blocks in closely related genomes, like different strains of the same bacterial species.
+
|Bowtie 2 is an ultrafast and memory-efficient tool for aligning sequencing reads  to long reference sequences. It is particularly good at aligning reads of about 50 up to 100s or 1,000s  of characters, and particularly good at aligning to relatively long (e.g. mammalian) genomes.  Bowtie 2 indexes the genome with an FM Index to keep its memory footprint small: for the human genome,  its memory footprint is typically around 3.2 GB. Bowtie 2 supports gapped, local, and paired-end alignment modes. - Homepage: http://bowtie-bio.sourceforge.net/bowtie2/index.shtml
 
|-
 
|-
|[http://www.cbs.dtu.dk/cgi-bin/nph-sw_request?signalp SignalP]
+
|[http://genome.ucsc.edu/FAQ/FAQblat.html BLAT]
|4.1
+
|3.5-IGB-gcc-4.9.4
|Signal peptide and cleavage sites in gram+, gram- and eukaryotic amino acid sequences
+
|BLAT on DNA is designed to quickly find sequences of 95% and greater similarity of length 25 bases or more.
 
|-
 
|-
|[http://http://sox.sourceforge.net/ SoX]
+
|[https://github.com/DRL/blobtools blobtools]
|14.4.2-IGB-gcc-4.9.4
+
|0.9.19.6-IGB-gcc-4.9.4-Python-2.7.13
|Sound eXchange, the Swiss Army knife of audio manipulation
+
|Application for the visualisation of (draft) genome assemblies using TAGC (Taxon-annotated Gc-Coverage) plots - Homepage: https://github.com/DRL/blobtools
 
|-
 
|-
|[http://vfsmspineagent.fsm.northwestern.edu/ Spine]
+
|[https://github.com/mateidavid/fast5 fast5]
|0.2.1-IGB-gcc-4.9.4
+
|0.6.2-IGB-gcc-4.9.4<br>0.6.3-IGB-gcc-4.9.4<br>0.6.5-IGB-gcc-4.9.4
|Spine identifies a core genome from input genomic sequences. Sequences are aligned using Nucmer and regions found to be in common between all or a user-defined subset of genomes will be returned.
+
|A lightweight C++ library for accessing Oxford Nanopore Technologies sequencing data.
 
|-
 
|-
|[http://creskolab.uoregon.edu/stacks/ Stacks]
+
|[https://github.com/nanoporetech/medaka medaka]
|1.47-IGB-gcc-4.9.4
+
|0.1.0-IGB-gcc-4.9.4-Python-3.6.1
|Stacks is a software pipeline for building loci from short-read sequences, such as those generated on the Illumina platform. Stacks was developed to work with restriction enzyme-based data, such as RAD-seq, for the purpose of building genetic maps and conducting population genomics and phylogeography.
+
|Medaka demonstrates a framework for error correcting sequencing data, particularly aimed at nanopore sequencing. Tools are provided for both training and inference. The code exploits the keras deep learning library.
 
|-
 
|-
|[http://ccb.jhu.edu/software/stringtie/ StringTie]
+
|[http://www.open-mpi.org/ OpenMPI]
|1.3.3-IGB-gcc-4.9.4
+
|2.1.0-GCC-4.9.4-2.28
|StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts. - Homepage: http://ccb.jhu.edu/software/stringtie/
+
|The Open MPI Project is an open source MPI-2 implementation.
 
|-
 
|-
|[http://subread.sourceforge.net/ Subread]
+
|[http://www.gnu.org/software/automake/automake.html Automake]
|1.5.2-IGB-gcc-4.9.4
+
|.1.15<br>.1.15-IGB-gcc-4.9.4
|High performance read alignment, quantification and mutation discovery - Homepage: http://subread.sourceforge.net/
+
|Automake: GNU Standards-compliant Makefile generator
 
|-
 
|-
|[https://support.10xgenomics.com/de-novo-assembly/software/overview/latest/welcome Supernova]
+
|[http://www.bioinformatics.babraham.ac.uk/projects/bismark/ Bismark]
|1.1.5<br>1.2.0<br>1.2.1<br>2.0.0<br>2.0.1<br>2.1.0<br>2.1.1
+
|0.17.0-IGB-gcc-4.9.4-Perl-5.24.1<br>0.18.1-IGB-gcc-4.9.4-Perl-5.24.1
|Supernova is a software package for de novo assembly from Chromium Linked-Reads that are made from a single whole-genome library from an individual DNA source. A key feature of Supernova is that it creates diploid assemblies, thus separately representing maternal and paternal chromosomes over very long distances.
+
|A tool to map bisulfite converted sequence reads and determine cytosine methylation states - Homepage: http://www.bioinformatics.babraham.ac.uk/projects/bismark/
 
|-
 
|-
|[http://www.hdfgroup.org/doc_resource/SZIP/ Szip]
+
|[http://hannonlab.cshl.edu/fastx_toolkit/ FASTX-Toolkit]
|.2.1.1-IGB-gcc-4.9.4
+
|0.0.14-IGB-gcc-4.9.4
|Szip compression software, providing lossless compression of scientific data - Homepage: http://www.hdfgroup.org/doc_resource/SZIP/
+
|The FASTX-Toolkit is a collection of command line tools for  Short-Reads FASTA/FASTQ files preprocessing. - Homepage: http://hannonlab.cshl.edu/fastx_toolkit/
 
|-
 
|-
|[http://www.maizegenetics.net/tassel TASSEL]
+
|[http://www.canonware.com/jemalloc jemalloc]
|5.2.28-Java-1.8.0_121
+
|5.0.1-IGB-gcc-4.9.4
|While TASSEL has changed considerably since its initial public release in 2001, its primary function continues to be providing tools to investigate the relationship between phenotypes and genotypes
+
|jemalloc is a general purpose malloc(3) implementation that emphasizes fragmentation avoidance and scalable concurrency support.
|-
 
|[http://www.cbs.dtu.dk/cgi-bin/nph-sw_request?tmhmm TMHMM]
 
|2.0c-IGB-gcc-4.9.4
 
|Transmembrane helices in proteins
 
|-
 
|[https://github.com/Generade-nl/TULIP TULIP]
 
|20170513-IGB-gcc-4.9.4-Perl-5.24.1
 
|Tulipseed takes as input alignments files of long reads to sparse short seeds, and outputs a graph and scaffold structures. Tulipbulb adds long read sequencing data to these.
 
|-
 
|[http://www.tcl.tk/ Tcl]
 
|8.6.6-IGB-gcc-4.9.4
 
|Tcl (Tool Command Language) is a very powerful but easy to learn dynamic programming language,suitable for a very wide range of uses, including web and desktop applications, networking, administration,testing and many more. - Homepage: http://www.tcl.tk/
 
 
|-
 
|-
 
|[https://github.com/tensorflow/models TensorFlowModels]
 
|[https://github.com/tensorflow/models TensorFlowModels]
Line 981: Line 973:
 
|This repository contains a number of different models implemented in TensorFlow:
 
|This repository contains a number of different models implemented in TensorFlow:
 
|-
 
|-
|[https://www.tensorflow.org/ Tensorflow]
+
|[http://www.hdfgroup.org/HDF5/ HDF5]
|1.2.1-IGB-gcc-4.9.4-Python-2.7.13
+
|1.8.18-IGB-gcc-4.9.4
|An open-source software library for Machine Intelligence
+
|HDF5 is a unique technology suite that makes possible the management of extremely large and complex data collections.
 
|-
 
|-
|[https://www.tensorflow.org/ Tensorflow-GPU]
+
|[http://xmlsoft.org/ libxml2]
|1.2.1-IGB-gcc-4.9.4-Python-3.6.1<br>1.5.1-IGB-gcc-4.9.4-Python-3.6.1
+
|2.9.4-IGB-gcc-4.9.4
|An open-source software library for Machine Intelligence
+
|Libxml2 is the XML C parser and toolchain developed for the Gnome project (but usable outside of the Gnome platform). - Homepage: http://xmlsoft.org/
 
|-
 
|-
|[http://deeplearning.net/software/theano Theano]
+
|[https://developer.gnome.org/gtk+/stable/ GTK+]
|0.9.0-IGB-gcc-4.9.4-Python-2.7.13
+
|2.24.31-IGB-gcc-4.9.4-Python-2.7.13<br>2.24.31-IGB-gcc-4.9.4-Python-3.6.1
|Theano is a Python library that allows you to define, optimize,and evaluate mathematical expressions involving multi-dimensional arrays efficiently. - Homepage: http://deeplearning.net/software/theano
+
|The GTK+ 2 package contains libraries used for creating graphical user interfaces for applications.
 
|-
 
|-
|[http://www.tcl.tk/ Tk]
+
|[http://libevent.org/ libevent]
|.8.6.6-IGB-gcc-4.9.4
+
|.2.1.8-IGB-gcc-4.9.4
|Tk is an open source, cross-platform widget toolchain that provides a library of basic elements for building a graphical user interface (GUI) in many different programming languages. - Homepage: http://www.tcl.tk/
+
|The libevent API provides a mechanism to execute a callback function when a specific event occurs on a file descriptor or after a timeout has been reached. Furthermore, libevent also support callbacks due to signals or regular timeouts. - Homepage: http://libevent.org/
 
|-
 
|-
|[http://ccb.jhu.edu/software/tophat/index.shtml TopHat]
+
|[https://github.com/gpertea/cdbfasta cdbfasta]
|1.4.1<br>2.1.1-IGB-gcc-4.9.4
+
|20170316-IGB-gcc-4.9.4
|TopHat is a fast splice junction mapper for RNA-Seq reads. It aligns RNA-Seq reads to mammalian-sized genomes using the ultra high-throughput short read aligner Bowtie, and then analyzes the mapping results to identify splice junctions between exons.
+
|CDB (Constant DataBase) indexing and retrieval tools for FASTA files
 
|-
 
|-
|[https://github.com/torch/distro Torch]
+
|[https://github.com/isovic/racon racon]
|20171018-IGB-gcc-4.9.4-Python-3.6.1
+
|0.5.0-IGB-gcc-4.9.4-Python-2.7.13<br>0.5.0-IGB-gcc-4.9.4-Python-3.6.1
|Torch is a scientific computing framework with wide support for machine learning algorithms that puts GPUs first. It is easy to use and efficient, thanks to an easy and fast scripting language, LuaJIT, and an underlying C/CUDA implementation.
+
|Racon is intended as a standalone consensus module to correct raw contigs generated by rapid assembly methods which do not include a consensus step, such as Miniasm.The goal of Racon is to generate genomic consensus which is of similar or better quality compared to the output generated by assembly methods which employ both error correction and consensus steps, while providing a speedup of several times compared to those methods.
 
|-
 
|-
|[https://github.com/TransDecoder/TransDecoder/wiki TransDecoder]
+
|[http://sourceforge.net/projects/snpeff/ snpEff]
|5.1.0-IGB-gcc-4.9.4-Perl-5.24.1
+
|4.3o-Java-1.8.0_121
|TransDecoder identifies candidate coding regions within transcript sequences, such as those generated by de novo RNA-Seq transcript assembly using Trinity, or constructed based on RNA-Seq alignments to the genome using Tophat and Cufflinks.
+
|SnpEff is a variant annotation and effect prediction tool.  It annotates and predicts the effects of genetic variants (such as amino acid changes).
 
|-
 
|-
|[http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/ Trim_Galore]
+
|[https://developer.nvidia.com/cudnn cuDNN]
|0.4.4-IGB-gcc-4.9.4
+
|5.1-IGB-gcc-4.9.4-CUDA-8.0.61<br>6.0-IGB-gcc-4.9.4-CUDA-8.0.61<br>7.0.5-IGB-gcc-4.9.4-CUDA-9.0.176<br>7.1.4-IGB-gcc-4.9.4-CUDA-9.0.176
|A wrapper tool around Cutadapt and FastQC to consistently apply  quality and adapter trimming to FastQ files, with some extra functionality for  MspI-digested RRBS-type (Reduced Representation Bisufite-Seq) libraries. - Homepage: http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/
+
|The NVIDIA CUDA Deep Neural Network library (cuDNN) is a GPU-accelerated library of primitives for    deep neural networks.
 
|-
 
|-
|[http://www.usadellab.org/cms/?page=trimmomatic Trimmomatic]
+
|IGB-gcc
|0.36-Java-1.8.0_121<br>0.36-Java-1.8.0_152<br>0.38-Java-1.8.0_152
+
|.4.9.4
|Trimmomatic performs a variety of useful trimming tasks for illumina paired-end and single ended data.The selection of trimming steps and their associated parameters are supplied on the command line.  
+
|GNU Compiler Collection (GCC) based compiler toolchain, including OpenMPI for MPI support, OpenBLAS (BLAS and LAPACK support), FFTW and ScaLAPACK.
 
|-
 
|-
|[http://trinityrnaseq.github.io/ Trinity]
+
|[https://faculty.washington.edu/browning/beagle/beagle.html beagle]
|2.4.0-IGB-gcc-4.9.4<br>2.5.0-IGB-gcc-4.9.4<br>2.6.5-IGB-gcc-4.9.4
+
|03Jul18.40b-Java-1.8.0_152
|Trinity represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-Seq data. Trinity combines three independent software modules: Inchworm, Chrysalis, and Butterfly, applied sequentially to process large volumes of RNA-Seq reads. - Homepage: http://trinityrnaseq.github.io/
+
|Beagle is a software package for phasing genotypes and for imputing ungenotyped markers. Version 5.0 has new, fast algorithms for genotype phasing and imputation.  
 
|-
 
|-
|[https://trinotate.github.io/ Trinotate]
+
|[https://github.com/tseemann/prokka prokka]
|3.1.1-IGB-gcc-4.9.4-Perl-5.24.1
+
|1.12-IGB-gcc-4.9.4-Perl-5.24.1<br>1.13-IGB-gcc-4.9.4-Perl-5.24.1
|Trinotate is a comprehensive annotation suite designed for automatic functional annotation of transcriptomes, particularly de novo assembled transcriptomes, from model or non-model organisms. Trinotate makes use of a number of different well referenced methods for functional annotation including homology search to known sequence data (BLAST+/SwissProt), protein domain identification (HMMER/PFAM), protein signal peptide and transmembrane domain prediction (signalP/tmHMM), and leveraging various annotation databases (eggNOG/GO/Kegg databases). All functional annotation data derived from the analysis of transcripts is integrated into a SQLite database which allows fast efficient searching for terms with specific qualities related to a desired scientific hypothesis or a means to create a whole annotation report for a transcriptome.
+
|Whole genome annotation is the process of identifying features of interest in a set of genomic DNA sequences, and labelling them with useful information. Prokka is a software tool to annotate bacterial, archaeal and viral genomes quickly and produce standards-compliant output files.
 
|-
 
|-
|[http://www.drive5.com/usearch/index.html USEARCH]
+
|[http://libgd.bitbucket.org/ libgd]
|6.1.544<br>7.0.1090<br>9.2.64
+
|.2.2.4-IGB-gcc-4.9.4
|USEARCH is a unique sequence analysis tool which offers search and clustering algorithms that are often orders of magnitude faster than BLAST.
+
|GD is an open source code library for the dynamic creation of images by programmers. - Homepage: http://libgd.bitbucket.org/
 
|-
 
|-
|[https://github.com/rrwick/Unicycler Unicycler]
+
|[http://easybuilders.github.com/easybuild/ EasyBuild]
|0.4.3-IGB-gcc-4.9.4-Python-3.6.1<br>0.4.4-IGB-gcc-4.9.4-Python-3.6.1
+
|3.5.3<br>3.6.0<br>3.6.2
|Unicycler is an assembly pipeline for bacterial genomes. It can assemble Illumina-only read sets where it functions as a SPAdes-optimiser. It can also assembly long-read-only sets (PacBio or Nanopore) where it runs a miniasm+Racon pipeline. For the best possible assemblies, give it both Illumina reads and long reads, and it will conduct a hybrid assembly.
+
|EasyBuild is a software build and installation frameworkwritten in Python that allows you to install software in a structured,repeatable and robust way.
 
|-
 
|-
|[https://vcftools.github.io VCFtools]
+
|[https://www.gnu.org/software/parallel/ parallel]
|0.1.15-IGB-gcc-4.9.4-Perl-5.24.1
+
|20170622-IGB-gcc-4.9.4
|The aim of VCFtools is to provide  easily accessible methods for working with complex  genetic variation data in the form of VCF files. - Homepage: https://vcftools.github.io
+
|parallel: GNU parallel is a shell tool for executing jobs in parallel using one or more computers.  
 
|-
 
|-
|[https://github.com/Ensembl/ensembl-vep VEP]
+
|[https://github.com/PacificBiosciences/GenomicConsensus GenomicConsensus]
|92.4-IGB-gcc-4.9.4-Perl-5.24.1
+
|3.0.2-IGB-gcc-4.9.4-Python-2.7.13
|VEP (Variant Effect Predictor) predicts the functional effects of genomic variants.
+
|The GenomicConsensus package provides the variantCaller tool, which allows you to apply the Quiver or Arrow algorithm to mapped PacBio reads to get consensus and variant calls.
 
|-
 
|-
|VICSIN
+
|[https://github.com/DReichLab/AdmixTools AdmixTools]
|0.5-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13<br>0.5.1-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13<br>0.5.2-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
+
|1.0.1-IGB-gcc-4.9.4
|VICSIN = Viral, Integrative, and Conjugative Sequence Identification and Networking
+
|The ADMIXTOOLS package implements 5 methods described in Patterson et al. (2012) Ancient Admixture in Human History. Details of the methods and algorithm can be found in this paper.
 
|-
 
|-
|[https://github.com/torognes/vsearch VSEARCH]
+
|efidb
|2.4.3-IGB-gcc-4.9.4
+
|ip62<br>ip63<br>ip64<br>ip65<br>ip66<br>ip66_private<br>ip67<br>ip68<br>ip69
|VSEARCH stands for vectorized search, as the tool takes advantage of parallelism in the form of SIMD vectorization as well as multiple threads to perform accurate alignments at high speed. - Homepage: https://github.com/torognes/vsearch
+
|
 
|-
 
|-
|[https://www.tbi.univie.ac.at/RNA/ ViennaRNA]
+
|[http://www.r-project.org/ R]
|2.4.2-IGB-gcc-4.9.4
+
|2.15.3-IGB-gcc-4.9.4<br>3.1.2-IGB-gcc-4.9.4<br>3.2.5-IGB-gcc-4.9.4<br>3.3.3-IGB-gcc-4.9.4<br>3.4.1-IGB-gcc-4.9.4<br>3.4.2-IGB-gcc-4.9.4<br>3.5.0-IGB-gcc-4.9.4
|The ViennaRNA Package consists of a C code library and several stand-alone programs for the prediction and comparison of RNA secondary structures.  
+
|R is a free software environment for statistical computing and graphics.
 
|-
 
|-
|[https://github.com/simroux/VirSorter VirSorter]
+
|[http://www.mothur.org/ Mothur]
|20170215-IGB-gcc-4.9.4-Perl-5.24.1
+
|1.38.1.1<br>1.39.5<br>1.39.5-IGB-gcc-4.9.4
|VirSorter: mining viral signal from microbial genomic data.
+
|Mothur is a single piece of open-source, expandable software to fill the bioinformatics needs of the microbial ecology community.
 
|-
 
|-
|[http://tukaani.org/xz/ XZ]
+
|[http://code.google.com/p/openpgm/ OpenPGM]
|.5.2.3-IGB-gcc-4.9.4
+
|5.2.122-IGB-gcc-4.9.4
|xz: XZ utilities
+
|OpenPGM is an open source implementation of the Pragmatic General Multicast (PGM) specification in RFC 3208 available at www.ietf.org. PGM is a reliable and scalable multicast protocol that enables receivers to detect loss, request retransmission of lost data, or notify an application of unrecoverable loss. PGM is a receiver-reliable protocol, which means the receiver is responsible for ensuring all data is received, absolving the sender of reception responsibility.
 
|-
 
|-
|[Complete rewrite of the NASM assembler with BSD license - Homepage: http://www.tortall.net/projects/yasm/ Yasm]
+
|[http://curl.haxx.se cURL]
|.1.3.0-IGB-gcc-4.9.4<br>1.3.0-IGB-gcc-4.9.4
+
|.7.53.1-IGB-gcc-4.9.4
|Yasm: Complete rewrite of the NASM assembler with BSD license - Homepage: http://www.tortall.net/projects/yasm/
+
|libcurl is a free and easy-to-use client-side URL transfer library, supporting DICT, FILE, FTP, FTPS, Gopher, HTTP, HTTPS, IMAP, IMAPS, LDAP, LDAPS, POP3, POP3S, RTMP, RTSP, SCP, SFTP, SMTP, SMTPS, Telnet and TFTP. libcurl supports SSL certificates, HTTP POST, HTTP PUT, FTP uploading, HTTP form based upload, proxies, cookies, user+password authentication (Basic, Digest, NTLM, Negotiate, Kerberos), file transfer resume, http proxy tunneling and more. - Homepage: http://curl.haxx.se
 
|-
 
|-
|[http://www.zeromq.org/ ZeroMQ]
+
|[http://www.littlecms.com/ LittleCMS]
|4.2.2-IGB-gcc-4.9.4
+
|.2.8-IGB-gcc-4.9.4<br>2.8-IGB-gcc-4.9.4
|ZeroMQ looks like an embeddable networking library but acts like a concurrency framework. It gives you sockets that carry atomic messages across various transports like in-process, inter-process, TCP, and multicast. You can connect sockets N-to-N with patterns like fanout, pub-sub, task distribution, and request-reply. It is fast enough to be the fabric for clustered products. Its asynchronous I/O model gives you scalable multicore applications, built as asynchronous message-processing tasks. It has a score of language APIs and runs on most operating systems.
+
|Little CMS intends to be an OPEN SOURCE small-footprint color management engine, with special focus on accuracy and performance. - Homepage: http://www.littlecms.com/
 
|-
 
|-
|[http://www-inf.enst.fr/~demaille/a2ps/ a2ps]
+
|[http://www.scons.org/ SCons]
|4.14-IGB-gcc-4.9.4
+
|3.0.1-IGB-gcc-4.9.4-Python-2.7.13<br>3.0.1-IGB-gcc-4.9.4-Python-3.6.1
|a2ps-4.14: Formats an ascii file for printing on a postscript printer
+
|SCons is a software construction tool.
 
|-
 
|-
|[http://www.genetics.ucla.edu/software/admixture/index.html admixture]
+
|[http://valgrind.org/downloads/ valgrind]
|1.3.0
+
|3.13.0-IGB-gcc-4.9.4
|ADMIXTURE is a software tool for maximum likelihood estimation of individual ancestries from multilocus SNP genotype datasets. It uses the same statistical model as STRUCTURE but calculates estimates much more rapidly using a fast numerical optimization algorithm.  
+
|Valgrind is an instrumentation framework for building dynamic analysis tools. There are Valgrind tools that can automatically detect many memory management and threading bugs, and profile your programs in detail. You can also use Valgrind to build new tools.
 
|-
 
|-
|[https://nanoporetech.com/ albacore]
+
|[http://www.broadinstitute.org/gatk/ GATK]
|2.0.2-IGB-gcc-4.9.4-Python-3.6.1<br>2.1.10-IGB-gcc-4.9.4-Python-3.6.1<br>2.3.1-IGB-gcc-4.9.4-Python-3.6.1
+
|3.7-Java-1.8.0_121<br>3.8-0-Java-1.8.0_152<br>3.8-1-0-Java-1.8.0_152<br>4.0.4.0-IGB-gcc-4.9.4-Java-1.8.0_152-Python-3.6.1
|Local basecalling for MinKNOW
+
|The Genome Analysis Toolkit or GATK is a software package developed at the Broad Institute to analyse next-generation resequencing data. The toolkit offers a wide variety of tools, with a primary focus on variant discovery and genotyping as well as strong emphasis on data quality assurance. Its robust architecture, powerful processing engine and high-performance computing features make it capable of taking on projects of any size.
 
|-
 
|-
|[http://ant.apache.org/ ant]
+
|[http://opensource.scilifelab.se/projects/cutadapt/ cutadapt]
|1.10.1-Java-1.8.0_121
+
|1.14-IGB-gcc-4.9.4-Python-2.7.13<br>1.17-IGB-gcc-4.9.4-Python-3.6.1
|Apache Ant is a Java library and command-line tool whose mission is to drive processes described in build files as targets and extension points dependent upon each other. The main known usage of Ant is the build of Java applications. - Homepage: http://ant.apache.org/
+
|Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads.  
 
|-
 
|-
|[http://argtable.sourceforge.net/ argtable]
+
|[http://www.gnu.org/software/libtool libtool]
|.2.13-IGB-gcc-4.9.4
+
|.2.4.6<br>.2.4.6-IGB-gcc-4.9.4
|Argtable is an ANSI C library for parsing GNU style command line options with a minimum of fuss. - Homepage: http://argtable.sourceforge.net/
+
|GNU libtool is a generic library support script. Libtool hides the complexity of using shared libraries behind a consistent, portable interface. - Homepage: http://www.gnu.org/software/libtool
 
|-
 
|-
|[http://asperasoft.com/ aspera]
+
|[http://cran.r-project.org/web/packages/ncdf4 ncdf4]
|3.7.6
+
|1.16-IGB-gcc-4.9.4-R-3.3.3
|Aspera’s unwavering mission is to create the next-generation software technologies that move the world’s data at maximum speed, regardless of file size, transfer distance and network conditions.
+
|This package provides a high-level R interface to data files written using Unidatas netCDF library (version 4 or earlier), which are binary data files that are portable across platforms and include metadata information in addition to the data sets.
 
|-
 
|-
|[http://atactk.readthedocs.io/ atactk]
+
|[https://www.mdc-berlin.de/8551903/en/ mirdeep]
|0.1.6-IGB-gcc-4.9.4-Python-2.7.13
+
|2.0.0.8-IGB-gcc-4.9.4
|a toolkit for ATAC-seq data
+
|miRDeep2 is a completely overhauled tool which discovers microRNA genes by analyzing sequenced RNAs.
 
|-
 
|-
|[http://bioinf.uni-greifswald.de/augustus/ augustus]
+
|[http://picrust.github.io/picrust/ PICRUSt]
|3.2.3-IGB-gcc-4.9.4
+
|1.1.1-IGB-gcc-4.9.4-Python-2.7.13<br>1.1.3-IGB-gcc-4.9.4-Python-2.7.13
|AUGUSTUS is a program that predicts genes in eukaryotic genomic sequences. - Homepage: http://bioinf.uni-greifswald.de/augustus/
+
|PICRUSt (pronounced pie crust) is a bioinformatics software package designed to predict metagenome functional content from marker gene (e.g., 16S rRNA) surveys and full genomes.
 
|-
 
|-
|[http://dna.ku.dk/%7Esapfo/bammds.html bammds]
+
|[http://cab.spbu.ru/software/spades/ SPAdes]
|20140602-IGB-gcc-4.9.4
+
|3.10.1-IGB-gcc-4.9.4-Python-2.7.13<br>3.11.0-IGB-gcc-4.9.4-Python-2.7.13<br>3.11.0-IGB-gcc-4.9.4-Python-3.6.1<br>3.11.1-IGB-gcc-4.9.4-Python-3.6.1
|Software that allows to create a multidimensional scaling (MDS) plot of populations for genetic data.
+
|SPAdes . St. Petersburg genome assembler . is intended for both standard isolates and single-cell MDA bacteria assemblies.
 
|-
 
|-
|[https://github.com/PacificBiosciences/bax2bam bax2bam]
+
|[http://samtools.sourceforge.net tabix]
|20171114-IGB-gcc-4.9.4
+
|0.2.6-IGB-gcc-4.9.4
|bax2bam converts the legacy PacBio basecall format (bax.h5) into the BAMbasecall format.
+
|Generic indexer for TAB-delimited genome position files
 
|-
 
|-
|[http://bazel.io/ bazel]
+
|[https://www.realtimegenomics.com/products/rtg-tools rtg-tools]
|0.6.0-Java-1.8.0_121
+
|3.8.4
|Bazel is a build tool that builds code quickly and reliably. It is used to build the majority of Googles software.
+
|RTG Tools contains utilities to easily manipulate and accurately compare multiple VCF files, as well as utilities for processing other common NGS data formats.
 
|-
 
|-
|[https://faculty.washington.edu/browning/beagle/beagle.html beagle]
+
|[https://github.com/ncbi/ngs NGS]
|03Jul18.40b-Java-1.8.0_152
+
|1.3.0-IGB-gcc-4.9.4
|Beagle is a software package for phasing genotypes and for imputing ungenotyped markers. Version 5.0 has new, fast algorithms for genotype phasing and imputation.  
+
|NGS is a new, domain-specific API for accessing reads, alignments and pileups produced from Next Generation Sequencing. - Homepage: https://github.com/ncbi/ngs
 
|-
 
|-
|[https://bedops.readthedocs.io/en/latest/ bedops]
+
|[http://nco.sourceforge.net NCO]
|2.4.30
+
|4.7.2-IGB-gcc-4.9.4
|BEDOPS is an open-source command-line toolkit that performs highly efficient and scalable Boolean and other set operations, statistical calculations, archiving, conversion and other management of genomic data of arbitrary scale.
+
|manipulates and analyzes data stored in netCDF-accessible formats, including DAP, HDF4, and HDF5
 
|-
 
|-
|[GNU binary utilities - Homepage: http://directory.fsf.org/project/binutils/ binutils]
+
|[http://github.com/wolever/nose-parameterized nose-parameterized]
|.2.28<br>.2.28-GCCcore-4.9.4
+
|0.6.0-IGB-gcc-4.9.4-Python-2.7.13
|binutils: GNU binary utilities - Homepage: http://directory.fsf.org/project/binutils/
+
|Parameterized testing with any Python test framework.
 
|-
 
|-
|[https://github.com/IGBIllinois/biodatabase/ biodatabase]
+
|[http://ab.inf.uni-tuebingen.de/software/megan6/ MEGAN]
|1.0-IGB-gcc-4.9.4
+
|6.12.2-Java-1.8.0_152
|Scripts to create databases on the biodatabase machine.
+
|MEGAN6 is a comprehensive toolbox for interactively analyzing microbiome data. All the interactive tools you need in one application.
 
|-
 
|-
|[http://biom-format.org/ biom-format]
+
|[http://busco.ezlab.org/ BUSCO]
|2.1.6-IGB-gcc-4.9.4-Python-2.7.13<br>2.1.6-IGB-gcc-4.9.4-Python-3.6.1
+
|3.0.1-IGB-gcc-4.9.4-Python-2.7.13
|The BIOM file format (canonically pronounced biome) is designed to be a general-use format for representing biological sample by observation contingency tables.
+
|BUSCO v3 provides quantitative measures for the assessment of genome assembly, gene set, and transcriptome completeness, based on evolutionarily-informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB v9.
 
|-
 
|-
|[https://github.com/DRL/blobtools blobtools]
+
|[http://www.ece.uvic.ca/~frodo/jasper/ JasPer]
|0.9.19.6-IGB-gcc-4.9.4-Python-2.7.13
+
|1.900.1-IGB-gcc-4.9.4<br>2.0.10-IGB-gcc-4.9.4
|Application for the visualisation of (draft) genome assemblies using TAGC (Taxon-annotated Gc-Coverage) plots - Homepage: https://github.com/DRL/blobtools
+
|The JasPer Project is an open-source initiative to provide a free software-based reference implementation of the codec specified in the JPEG-2000 Part-1 standard. - Homepage: http://www.ece.uvic.ca/~frodo/jasper/
 
|-
 
|-
|[https://github.com/barricklab/breseq breseq]
+
|[https://xiph.org/flac/ FLAC]
|0.31.0-IGB-gcc-4.9.4
+
|1.3.1-IGB-gcc-4.9.4
|is a computational pipeline for the analysis of short-read re-sequencing data (e.g. Illumina, 454, IonTorrent, etc.). It uses reference-based alignment approaches to predict mutations in a sample relative to an already sequenced genome.
+
|Programs and libraries for working with Free Lossless Audio Codec (FLAC) files.
 
|-
 
|-
|[http://invisible-island.net/byacc/byacc.html byacc]
+
|[https://github.com/PacificBiosciences/bax2bam bax2bam]
|20170709-IGB-gcc-4.9.4
+
|20171114-IGB-gcc-4.9.4
|Berkeley Yacc (byacc) is generally conceded to be the best yacc variant available.In contrast to bison, it is written to avoid dependencies upon a particular compiler.
+
|bax2bam converts the legacy PacBio basecall format (bax.h5) into the BAMbasecall format.  
 
|-
 
|-
|[http://www.bzip.org/ bzip2]
+
|[http://www-huber.embl.de/users/anders/HTSeq/ HTSeq]
|1.0.6-IGB-gcc-4.9.4
+
|0.9.0-IGB-gcc-4.9.4-Python-2.7.13<br>0.9.1-IGB-gcc-4.9.4-Python-2.7.13
|bzip2 is a freely available, patent free, high-quality data compressor. It typically compresses files to within 10% to 15% of the best available techniques (the PPM family of statistical compressors), whilst being around twice as fast at compression and six times faster at decompression. - Homepage: http://www.bzip.org/
+
|A framework to process and analyze data from high-throughput sequencing (HTS) assays
 
|-
 
|-
|[http://curl.haxx.se cURL]
+
|[http://www.sanger.ac.uk/science/tools/ssaha2-0 ssaha_pileup]
|.7.53.1-IGB-gcc-4.9.4
+
|0.6-IGB-gcc-4.9.4
|libcurl is a free and easy-to-use client-side URL transfer library, supporting DICT, FILE, FTP, FTPS, Gopher, HTTP, HTTPS, IMAP, IMAPS, LDAP, LDAPS, POP3, POP3S, RTMP, RTSP, SCP, SFTP, SMTP, SMTPS, Telnet and TFTP. libcurl supports SSL certificates, HTTP POST, HTTP PUT, FTP uploading, HTTP form based upload, proxies, cookies, user+password authentication (Basic, Digest, NTLM, Negotiate, Kerberos), file transfer resume, http proxy tunneling and more. - Homepage: http://curl.haxx.se
+
|SSAHA2: Sequence Search and Alignment by Hashing Algorithm
 
|-
 
|-
|[https://github.com/ComparativeGenomicsToolkit/cactus cactus]
+
|[http://search.cpan.org/~lds/GD/ GD]
|20180705-IGB-gcc-4.9.4-Python-2.7.13
+
|2.66-IGB-gcc-4.9.4-Perl-5.24.1
|Cactus is a reference-free whole-genome multiple alignment program.
+
|GD.pm - Interface to Gd Graphics Library
 
|-
 
|-
|[http://cairographics.org cairo]
+
|[https://ccb.jhu.edu/software/hisat2/index.shtml HISAT2]
|1.14.8-IGB-gcc-4.9.4
+
|2.0.5-IGB-gcc-4.9.4
|Cairo is a 2D graphics library with support for multiple output devices. Currently supported output targets include the X Window System (via both Xlib and XCB), Quartz, Win32, image buffers, PostScript, PDF, and SVG file output. Experimental backends include OpenGL, BeOS, OS/2, and DirectFB - Homepage: http://cairographics.org
+
|HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) against the general human population (as well as against a single reference genome). - Homepage: https://ccb.jhu.edu/software/hisat2/index.shtml
 
|-
 
|-
|[https://github.com/gpertea/cdbfasta cdbfasta]
+
|[http://www.gnu.org/software/gettext/ gettext]
|20170316-IGB-gcc-4.9.4
+
|.0.19.8<br>.0.19.8-IGB-gcc-4.9.4
|CDB (Constant DataBase) indexing and retrieval tools for FASTA files
+
|GNU gettext is an important step for the GNU Translation Project, as it is an asset on which we maybuild many other steps. This package offers to programmers, translators, and even users, a well integrated set of toolsand documentation
 
|-
 
|-
|[https://support.10xgenomics.com/single-cell-gene-expression/software/pipelines/latest/what-is-cell-ranger cellranger]
+
|[http://orthomcl.org/ OrthoMCL]
|2.1.0<br>2.1.1
+
|2.0.9-IGB-gcc-4.9.4-Perl-5.24.1
|Cell Ranger is a set of analysis pipelines that process Chromium single cell 3 RNA-seq output to align reads, generate gene-cell matrices and perform clustering and gene expression analysis.
+
|OrthoMCL is a genome-scale algorithm for grouping orthologous protein sequences. - Homepage: http://orthomcl.org/
 
|-
 
|-
|[https://ccb.jhu.edu/software/centrifuge/ centrifuge]
+
|[http://www.videolan.org/developers/x264.html x264]
|1.0.3-beta-IGB-gcc-4.9.4<br>1.0.4-beta-IGB-gcc-4.9.4
+
|.20170604-IGB-gcc-4.9.4
|Centrifuge is a very rapid and memory-efficient system for the classification of DNA sequences from microbial samples, with better sensitivity than and comparable accuracy to other leading systems.
+
|x264 is a free software library and application for encoding video streams into the H.264/MPEG-4 AVC compression format, and is released under the terms of the GNU GPL. - Homepage: http://www.videolan.org/developers/x264.html
 
|-
 
|-
|[http://www.biostat.jhsph.edu/~hji/cisgenome/ cisgenome]
+
|[http://www.genome.umd.edu/masurca.html MaSuRCA]
|2.0-IGB-gcc-4.9.4
+
|3.2.3-IGB-gcc-4.9.4
|An integrated tool for tiling array, ChIP-seq, genome and cis-regulatory element analysis
+
|MaSuRCA is whole genome assembly software. It combines the efficiency of the de Bruijn graph  and Overlap-Layout-Consensus (OLC) approaches. MaSuRCA can assemble data sets containing  only short reads from Illumina sequencing or a mixture of short reads and long reads  (Sanger, 454, Pacbio and Nanopore).
 
|-
 
|-
|[http://clusterflow.io/ clusterflow]
+
|[https://github.com/kundajelab/idr IDR]
|0.5-IGB-gcc-4.9.4-Perl-5.25.1
+
|2.0.4-IGB-gcc-4.9.4-Python-3.6.1
|Cluster Flow is workflow manager designed to run bioinformatics pipelines. It is operated through a single command cf, which can be used to launch, configure, monitor and cancel pipelines.
+
|The IDR (Irreproducible Discovery Rate) framework is a unified approach to measure the reproducibility of findings identified from replicate experiments and provide highly stable thresholds based on reproducibility. Unlike the usual scalar measures of reproducibility, the IDR approach creates a curve, which quantitatively assesses when the findings are no longer consistent across replicates. In laymans terms, the IDR method compares a pair of ranked lists of identifications (such as ChIP-seq peaks).
 
|-
 
|-
|[http://www.gnu.org/software/coreutils/coreutils.html coreutils]
+
|[https://github.com/PacificBiosciences/unanimity/ unanimity]
|8.28-IGB-gcc-4.9.4
+
|20180307-IGB-gcc-4.9.4
|The GNU Core Utilities are the basic file, shell and text manipulation utilities of the GNU operating system.These are the core utilities which are expected to exist on every operating system.
+
|C++ library and its applications to generate and process accurate consensus sequences
 
|-
 
|-
|[https://developer.nvidia.com/cudnn cuDNN]
+
|shortbred/devlocal
|5.1-IGB-gcc-4.9.4-CUDA-8.0.61<br>6.0-IGB-gcc-4.9.4-CUDA-8.0.61<br>7.0.5-IGB-gcc-4.9.4-CUDA-9.0.176<br>7.1.4-IGB-gcc-4.9.4-CUDA-9.0.176
+
|devlocal
|The NVIDIA CUDA Deep Neural Network library (cuDNN) is a GPU-accelerated library of primitives for    deep neural networks.
+
|
 
|-
 
|-
|[http://opensource.scilifelab.se/projects/cutadapt/ cutadapt]
+
|[http://www.gnu.org/software/bison Bison]
|1.14-IGB-gcc-4.9.4-Python-2.7.13<br>1.17-IGB-gcc-4.9.4-Python-3.6.1
+
|.3.0.4<br>.3.0.4-GCCcore-4.9.4
|Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads.  
+
|Bison is a general-purpose parser generator that converts an annotated context-free grammarinto a deterministic LR or generalized LR (GLR) parser employing LALR(1) parser tables. - Homepage: http://www.gnu.org/software/bison
 
|-
 
|-
|[https://github.com/fidelram/deepTools deepTools]
+
|[http://atactk.readthedocs.io/ atactk]
|2.5.3-IGB-gcc-4.9.4-Python-2.7.13<br>3.0.1-IGB-gcc-4.9.4-Python-2.7.13
+
|0.1.6-IGB-gcc-4.9.4-Python-2.7.13
|deepTools addresses the challenge of handling the large amounts of data that are now routinely generated from DNA sequencing centers. deepTools contains useful modules to process the mapped reads data for multiple quality checks, creating normalized coverage files in standard bedGraph and bigWig file formats, that allow comparison between different files (for example, treatment and control). Finally, using such normalized and standardized files, deepTools can create many publication-ready visualizations to identify enrichments and for functional annotations of the genome.
+
|a toolkit for ATAC-seq data
 
|-
 
|-
|[https://github.com/spragunr/deep_q_rl deep_q_rl]
+
|[https://www.mathworks.com/help/matlab/matlab-engine-for-python.html MATLAB-python]
|20160603-IGB-gcc-4.9.4-Python-2.7.13
+
|2017b-IGB-gcc-4.9.4-Python-3.6.1
|This package provides a Lasagne/Theano-based implementation of the deep Q-learning algorithm described in:Playing Atari with Deep Reinforcement Learning Volodymyr Mnih, Koray Kavukcuoglu, David Silver, Alex Graves, Ioannis Antonoglou, Daan Wierstra, Martin RiedmillerandMnih, Volodymyr, et al. "Human-level control through deep reinforcement learning." Nature 518.7540 (2015): 529-533.
+
|The MATLAB Engine API for Python provides a package for Python to call MATLAB as a computational engine. The engine supports the reference implementation (CPython) for Python versions 2.7, 3.5, and 3.6.
 
|-
 
|-
|[https://github.com/shenlab-sinai/diffreps diffReps]
+
|[http://www.hdfgroup.org/doc_resource/SZIP/ Szip]
|1.55.6-IGB-gcc-4.9.4-Perl-5.24.1
+
|.2.1.1-IGB-gcc-4.9.4
|ChIP-seq is now widely used to profile the protein DNA interactions on a genome. It is of high interest to compare the differential enrichment of a histone mark or transcription factor between two contrasting conditions, such as disease vs. control. diffReps is developed to serve this purpose. It scans the whole genome using a sliding window, performing millions of statistical tests and report the significant hits. - Homepage: https://github.com/shenlab-sinai/diffreps
+
|Szip compression software, providing lossless compression of scientific data - Homepage: http://www.hdfgroup.org/doc_resource/SZIP/
 
|-
 
|-
|[http://expressionanalysis.github.io/ea-utils/ ea-utils]
+
|[https://github.com/Generade-nl/TULIP TULIP]
|1.04.807-IGB-gcc-4.9.4
+
|20170513-IGB-gcc-4.9.4-Perl-5.24.1
|Command-line tools for processing biological sequencing data. Barcode demultiplexing, adapter trimming, etc. Primarily written to support an Illumina based pipeline - but should work with any FASTQs.
+
|Tulipseed takes as input alignments files of long reads to sparse short seeds, and outputs a graph and scaffold structures. Tulipbulb adds long read sequencing data to these.
 
|-
 
|-
|[https://github.com/DReichLab/EIG eigensoft]
+
|[http://autotools.io Autotools]
|7.2.1-IGB-gcc-4.9.4
+
|.20150215<br>.20150215-IGB-gcc-4.9.4
|The EIGENSOFT package combines functionality from our population genetics methods (Patterson et al. 2006) and our EIGENSTRAT stratification correction method (Price et al. 2006).
+
|This bundle collect the standard GNU build tools: Autoconf, Automake and libtool
 
|-
 
|-
|[https://github.com/biocore-ntnu/epic epic]
+
|[http://llvm.org/ LLVM]
|0.2.9-IGB-gcc-4.9.4-Python-2.7.13
+
|4.0.1-IGB-gcc-4.9.4<br>6.0.0-IGB-gcc-4.9.4
|epic is a software package for finding medium to diffusely enriched domains in chip-seq data. It is a fast, parallel and memory-efficient implementation of the incredibly popular SICER algorithm.  
+
|The LLVM Core libraries provide a modern source- and target-independent optimizer, along with code generation support for many popular CPUs (as well as some less common ones!) These libraries are built around a well specified code representation known as the LLVM intermediate representation ("LLVM IR"). The LLVM Core libraries are well documented, and it is particularly easy to invent your own language (or port an existing compiler) to use LLVM as an optimizer and code generator.
 
|-
 
|-
|[https://www.ebi.ac.uk/about/vertebrate-genomics/software/exonerate exonerate]
+
|[https://nanoporetech.com/ albacore]
|2.2.0-IGB-gcc-4.9.4
+
|2.0.2-IGB-gcc-4.9.4-Python-3.6.1<br>2.1.10-IGB-gcc-4.9.4-Python-3.6.1<br>2.3.1-IGB-gcc-4.9.4-Python-3.6.1
|Exonerate is a generic tool for pairwise sequence comparison. It allows you to align sequences using a many alignment models, either exhaustive dynamic programming or a variety of heuristics.
+
|Local basecalling for MinKNOW
 
|-
 
|-
|[http://expat.sourceforge.net/ expat]
+
|[http://ccb.jhu.edu/software/stringtie/ StringTie]
|2.2.0-IGB-gcc-4.9.4
+
|1.3.3-IGB-gcc-4.9.4
|Expat is an XML parser library written in C. It is a stream-oriented parser in which an application registers handlers for things the parser might find in the XML document (like start tags) - Homepage: http://expat.sourceforge.net/
+
|StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts. - Homepage: http://ccb.jhu.edu/software/stringtie/
 
|-
 
|-
|[https://github.com/mateidavid/fast5 fast5]
+
|[http://weizhong-lab.ucsd.edu/cd-hit/ CD-HIT]
|0.6.2-IGB-gcc-4.9.4<br>0.6.3-IGB-gcc-4.9.4<br>0.6.5-IGB-gcc-4.9.4
+
|4.6.6-IGB-gcc-4.9.4
|A lightweight C++ library for accessing Oxford Nanopore Technologies sequencing data.
+
|CD-HIT is a very widely used program for clustering and  comparing protein or nucleotide sequences. - Homepage: http://weizhong-lab.ucsd.edu/cd-hit/
 
|-
 
|-
|[https://github.com/adrianlopezroche/fdupes fdupes]
+
|[https://mathgen.stats.ox.ac.uk/impute/impute_v2.html impute2]
|1.6.1-IGB-gcc-4.9.4
+
|2.3.2
|FDUPES is a program for identifying duplicate files residingwithin specified directories.
+
|IMPUTE2 is freely available for academic use. To see rules for non-academic use, please read the LICENCE file, which is included with each software download.  
 
|-
 
|-
|[http://www.darwinsys.com/file/ file]
+
|[https://support.10xgenomics.com/single-cell-gene-expression/software/pipelines/latest/what-is-cell-ranger cellranger]
|.5.30-IGB-gcc-4.9.4
+
|2.1.0<br>2.1.1
|The file command is a file type guesser, that is, a command-line tool that tells you in words what kind of data a file contains.
+
|Cell Ranger is a set of analysis pipelines that process Chromium single cell 3 RNA-seq output to align reads, generate gene-cell matrices and perform clustering and gene expression analysis.
 
|-
 
|-
|[http://flex.sourceforge.net/ flex]
+
|[http://blast.ncbi.nlm.nih.gov/ BLAST+]
|.2.6.3<br>.2.6.3-GCCcore-4.9.4
+
|2.6.0-IGB-gcc-4.9.4<br>2.7.1-IGB-gcc-4.9.4<br>2.8.0-IGB-gcc-4.9.4-alpha
|Flex (Fast Lexical Analyzer) is a tool for generating scanners. A scanner, sometimes called a tokenizer, is a program which recognizes lexical patterns in text. - Homepage: http://flex.sourceforge.net/
+
|Basic Local Alignment Search Tool, or BLAST, is an algorithm for comparing primary biological sequence information, such as the amino-acid sequences of different proteins or the nucleotides of DNA sequences.
 
|-
 
|-
|[https://github.com/seqan/flexbar flexbar]
+
|[http://emboss.sourceforge.net/ EMBOSS]
|3.0.3-IGB-gcc-4.9.4
+
|6.6.0-IGB-gcc-4.9.4-Java-1.8.0_121
|The program Flexbar preprocesses high-throughput sequencing data efficiently. It demultiplexes barcoded runs and removes adapter sequences. Moreover, trimming and filtering features are provided.  
+
|EMBOSS, The European Molecular Biology Open Software Suite. EMBOSS is a free Open Source software analysis package specially developed for the needs of the molecular biology (e.g. EMBnet) user community.
 
|-
 
|-
|[http://www.freedesktop.org/software/fontconfig fontconfig]
+
|[http://pachterlab.github.io/kallisto/ kallisto]
|2.12.1-IGB-gcc-4.9.4
+
|0.43.1-IGB-gcc-4.9.4<br>0.44.0-IGB-gcc-4.9.4
|Fontconfig is a library designed to provide system-wide font configuration, customization andapplication access. - Homepage: http://www.freedesktop.org/software/fontconfig
+
|kallisto is a program for quantifying abundances of transcripts from RNA-Seq data, or more generally of target sequences using high-throughput sequencing reads.
 
|-
 
|-
|[http://freetype.org freetype]
+
|[http://genometools.org/ genometools]
|2.7.1-IGB-gcc-4.9.4
+
|1.5.10-IGB-gcc-4.9.4
|FreeType 2 is a software font engine that is designed to be small, efficient, highly customizable, and portable while capable of producing high-quality output (glyph images). It can be used in graphics libraries, display servers, font conversion tools, text image generation tools, and many other products as well. - Homepage: http://freetype.org
+
|The GenomeTools genome analysis system is a free collection of bioinformatics tools (in the realm of genome informatics) combined into a single binary named gt. It is based on a C library named “libgenometools” which consists of several modules.
 
|-
 
|-
|[http://www.gnu.org/software/gdb/gdb.html gdb]
+
|[https://github.com/dstreett/FLASH2 FLASH2]
|8.0.1-IGB-gcc-4.9.4-Python-2.7.13
+
|2.2.00-IGB-gcc-4.9.4
|The GNU Project Debugger
+
|FLASH (Fast Length Adjustment of SHort reads) is an accurate and fast toolto merge paired-end reads that were generated from DNA fragments whoselengths are shorter than twice the length of reads. Merged read pairs resultin unpaired longer reads, which are generally more desired in genomeassembly and genome analysis processes.
 
|-
 
|-
|[https://gdc.cancer.gov/access-data/gdc-data-transfer-tool gdc-client]
+
|[http://creskolab.uoregon.edu/stacks/ Stacks]
|1.3.0-IGB-gcc-4.9.4-Python-2.7.13
+
|1.47-IGB-gcc-4.9.4
|The GDC Data Transfer Tool Client provides a command-line interface supporting both GDC data downloads and submissions.
+
|Stacks is a software pipeline for building loci from short-read sequences, such as those generated on the Illumina platform. Stacks was developed to work with restriction enzyme-based data, such as RAD-seq, for the purpose of building genetic maps and conducting population genomics and phylogeography.
 
|-
 
|-
|[http://www1.montpellier.inra.fr/CBGP/software/GeneClass/ geneclass]
+
|[http://sanger-pathogens.github.io/circlator/ Circlator]
|2.0
+
|1.5.1-IGB-gcc-4.9.4-Python-3.6.1
|GeneClass2 is a program employing multilocus genotypes to select or exclude populations as origins of individuals (Assignment and Migrants Detection). This is a completely rewritten new version that includes pop100gene features.
+
|A tool to circularize genome assemblies.  
 
|-
 
|-
|[https://www.gnu.org/software/gengetopt/gengetopt.html gengetopt]
+
|[http://www.pcre.org/ PCRE]
|.2.22.6-IGB-gcc-4.9.4
+
|.8.40-IGB-gcc-4.9.4
|Gengetopt is a tool to write command line option parsing code for C programs. - Homepage: https://www.gnu.org/software/gengetopt/gengetopt.html
+
|The PCRE library is a set of functions that implement regular expression pattern matching using the same syntax and semantics as Perl 5. - Homepage: http://www.pcre.org/
 
|-
 
|-
|[http://genometools.org/ genometools]
+
|[https://github.com/LynchLab/MAPGD MAPGD]
|1.5.10-IGB-gcc-4.9.4
+
|0.4.26-IGB-gcc-4.9.4
|The GenomeTools genome analysis system is a free collection of bioinformatics tools (in the realm of genome informatics) combined into a single binary named gt. It is based on a C library named “libgenometools” which consists of several modules.
+
|MAPGD is a series of related programs that estimate allele frequency, heterozygosity, Hardy-Weinberg disequilibrium, linkage disequilibrium and identity-by-descent (IBD) coefficients from population genomic data using a statistically rigorous maximum likelihood approach.
 
|-
 
|-
|[http://www.gnu.org/software/gettext/ gettext]
+
|[http://gcc.gnu.org/ GCC]
|.0.19.8<br>.0.19.8-IGB-gcc-4.9.4
+
|.4.9.4-2.28
|GNU gettext is an important step for the GNU Translation Project, as it is an asset on which we maybuild many other steps. This package offers to programmers, translators, and even users, a well integrated set of toolsand documentation
+
|The GNU Compiler Collection includes front ends for C, C++, Objective-C, Fortran, Java, and Ada, as well as libraries for these languages (libstdc++, libgcj,...). - Homepage: http://gcc.gnu.org/
 
|-
 
|-
|[http://ccb.jhu.edu/software/stringtie/gff.shtml gffread]
+
|[http://pandoc.org pandoc]
|ba7535f-IGB-gcc-4.9.4
+
|2.2.3.2
|The program gffread can be used to validate, filter, convert and perform various other operations on GFF files
+
|If you need to convert files from one markup format into another, pandoc is your swiss-army knife
 
|-
 
|-
|[http://git-scm.com/ git]
+
|[http://computation.llnl.gov/projects/sundials SUNDIALS]
|2.9.5-IGB-gcc-4.9.4
+
|2.6.2-IGB-gcc-4.9.4
|Git is a free and open source distributed version control system designedto handle everything from small to very large projects with speed and efficiency.
+
|SUNDIALS: SUite of Nonlinear and DIfferential/ALgebraic Equation Solvers
 
|-
 
|-
|[https://git-lfs.github.com/ git-lfs]
+
|[https://ccb.jhu.edu/software/centrifuge/ centrifuge]
|2.2.1-IGB-gcc-4.9.4
+
|1.0.3-beta-IGB-gcc-4.9.4<br>1.0.4-beta-IGB-gcc-4.9.4
|Git Large File Storage (LFS) replaces large files such as audio samples, videos,  datasets, and graphics with text pointers inside Git, while storing the file contents on a remote server  like GitHub.com or GitHub Enterprise.
+
|Centrifuge is a very rapid and memory-efficient system for the classification of DNA sequences from microbial samples, with better sensitivity than and comparable accuracy to other leading systems.
 
|-
 
|-
 
|[http://www.freedesktop.org/wiki/Software/xlibs glproto]
 
|[http://www.freedesktop.org/wiki/Software/xlibs glproto]
Line 1,293: Line 1,285:
 
|X protocol and ancillary headers
 
|X protocol and ancillary headers
 
|-
 
|-
|[http://gnuplot.sourceforge.net/ gnuplot]
+
|[http://tandem.bu.edu/trf/trf.html trf]
|4.6.7-IGB-gcc-4.9.4<br>5.0.6-IGB-gcc-4.9.4
+
|4.0.9
|Portable interactive, function plotting utility - Homepage: http://gnuplot.sourceforge.net/
+
|Tandem Repeats Finder is a program to locate and display tandem repeats in DNA sequences.  
 
|-
 
|-
|[(none) gompi]
+
|[https://www.gnu.org/software/gengetopt/gengetopt.html gengetopt]
|.4.9.4
+
|.2.22.6-IGB-gcc-4.9.4
|GNU Compiler Collection (GCC) based compiler toolchain, including OpenMPI for MPI support. - Homepage: (none)
+
|Gengetopt is a tool to write command line option parsing code for C programs. - Homepage: https://www.gnu.org/software/gengetopt/gengetopt.html
 
|-
 
|-
|[https://github.com/data61/gossamer gossamer]
+
|[https://github.com/PacificBiosciences/minorseq/blob/54ac795d7c119d21a4611d91ac458cd3e2e2b30a/doc/INSTALL.md minorseq]
|20170105-IGB-gcc-4.9.4
+
|20180314-IGB-gcc-4.9.4
|The gossamer bioinformatics suite contains goss, gossple, xenome, and electus
+
|Minor Variant Calling and Phasing Tools
 
|-
 
|-
|[https://www.gnu.org/software/gperf/ gperf]
+
|[http://tensorly.org/stable/home.html tensorly]
|3.1-IGB-gcc-4.9.4
+
|0.4.2-IGB-gcc-4.9.4-Python-3.6.1
|GNU gperf is a perfect hash function generator. For a given list of strings, it produces a hash function and hash table, in form of C or C++ code, for looking up a value depending on the input string. The hash function is perfect, which means that the hash table has no collisions, and the hash table lookup needs a single string comparison only.
+
|Simple and Fast Tensor Learning in Python
 
|-
 
|-
|[https://bitbucket.org/nsegata/graphlan/ graphlan]
+
|[http://www.bcgsc.ca/platform/bioinfo/software/links LINKS]
|6ca8735-IGB-gcc-4.9.4-Python-2.7.13
+
|1.8.5-IGB-gcc-4.9.4-Perl-5.24.1
|GraPhlAn is a software tool for producing high-quality circular representations of taxonomic and phylogenetic trees. It focuses on concise, integrative, informative, and publication-ready representations of phylogenetically- and taxonomically-driven investigation.
+
|LINKS is a scalable genomics application for scaffolding or re-scaffolding genome assembly drafts with long reads, such as those produced by Oxford Nanopore Technologies Ltd and Pacific Biosciences. It provides a generic alignment-free framework for scaffolding and can work on any sequences. It is versatile and supports not only long sequences as a source of long-range information, but also MPET pairs and linked-reads, such as those from the 10X Genomics GemCode and Chromium platform, via ARCS (http://www.bcgsc.ca/platform/bioinfo/software/arcs). Fill gaps in LINKS-derived scaffolds using Sealer (http://www.bcgsc.ca/platform/bioinfo/software/sealer).
 
|-
 
|-
|[https://github.com/DecodeGenetics/graphtyper graphtyper]
+
|[https://ninja-build.org/ ninja]
|1.3-IGB-gcc-4.9.4
+
|1.8.2-IGB-gcc-4.9.4
|Graphtyper is a highly scalable genotyping software. It represents a reference genome and known variants of a genomic region using an acyclic mathematical graph structure (a "pangenome reference"), which high-throughput sequence reads are re-aligned to for the purpose of discovering and genotyping SNPs and small indels.
+
|Ninja is a small build system with a focus on speed. It differs from other build systems in two major respects: it is designed to have its input files generated by a higher-level build system, and it is designed to run builds as fast as possible.
 
|-
 
|-
|[http://www.graphviz.org/ graphviz]
+
|[https://github.com/torch/distro Torch]
|2.40.1-IGB-gcc-4.9.4<br>2.40.1-IGB-gcc-4.9.4-Python-2.7.13
+
|20171018-IGB-gcc-4.9.4-Python-3.6.1
|Graphviz is open source graph visualization software. Graph visualization is a way of representing structural information as diagrams of abstract graphs and networks. It has important applications in networking, bioinformatics,  software engineering, database and web design, machine learning, and in visual interfaces for other technical domains.
+
|Torch is a scientific computing framework with wide support for machine learning algorithms that puts GPUs first. It is easy to use and efficient, thanks to an easy and fast scripting language, LuaJIT, and an underlying C/CUDA implementation.
 
|-
 
|-
|[https://github.com/google/googletest gtest]
+
|[http://ccb.jhu.edu/software/tophat/index.shtml TopHat]
|1.8.0-IGB-gcc-4.9.4
+
|1.4.1<br>2.1.1-IGB-gcc-4.9.4
|Googles C++ test framework
+
|TopHat is a fast splice junction mapper for RNA-Seq reads. It aligns RNA-Seq reads to mammalian-sized genomes using the ultra high-throughput short read aligner Bowtie, and then analyzes the mapping results to identify splice junctions between exons.
 
|-
 
|-
|[http://www.well.ox.ac.uk/~cfreeman/software/gwas/gtool.html gtool]
+
|[http://icorn.sourceforge.net/documentation.html icorn]
|0.7.5
+
|0.97-IGB-gcc-4.9.4
|GTOOL is a program for transforming sets of genotype data for use with the programs SNPTEST and IMPUTE.
+
|Inputs: Reference Sequence (FASTA) & reads (FASTQ) & information of short reads
 
|-
 
|-
|[https://cran.r-project.org/web/packages/h2o/index.html h2o]
+
|[https://symas.com/lmdb LMDB]
|3.14.0.3-IGB-gcc-4.9.4-R-3.3.3
+
|0.9.22-IGB-gcc-4.9.4
|R scripting functionality for H2O, the open source math engine for big data that computes parallel distributed machine learning algorithms such as generalized linear models, gradient boosting machines, random forests, and neural networks (deep learning) within various cluster environments.
+
|LMDB is a fast, memory-efficient database. With memory-mapped files, it has the read performance of a pure in-memory database while retaining the persistence of standard disk-based databases.
 
|-
 
|-
|[https://github.com/arq5x/poretools h5py]
+
|[http://www1.montpellier.inra.fr/CBGP/diyabc/index.php DIYABC]
|.2.7.0-IGB-gcc-4.9.4-Python-2.7.13<br>2.7.0-IGB-gcc-4.9.4-Python-2.7.13
+
|2.1.0
|a toolkit for working with nanopore sequencing data from Oxford Nanopore. - Homepage: https://github.com/arq5x/poretools
+
|a user-friendly approach to Approximate Bayesian Computation for inference on population history using molecular markers
 
|-
 
|-
|[https://www.gnu.org/software/help2man/ help2man]
+
|[http://www.primer3.org primer3]
|.1.47.4<br>.1.47.4-GCCcore-4.9.4<br>.1.47.4-GCCcore-7.3.0
+
|2.4.0-IGB-gcc-4.9.4
|help2man produces simple manual pages from the --help and --version output of other commands.
+
|Primer3 is a widely used program for designing PCR primers (PCR = "Polymerase Chain Reaction"). PCR is an essential and ubiquitous tool in genetics and molecular biology. Primer3 can also design hybridization probes and sequencing primers.  
 
|-
 
|-
|[http://www.open-mpi.org/projects/hwloc/ hwloc]
+
|[http://ccb.jhu.edu/software/stringtie/gff.shtml gffread]
|.1.11.6-GCC-4.9.4-2.28
+
|ba7535f-IGB-gcc-4.9.4
|The Portable Hardware Locality (hwloc) software package provides a portable abstraction(across OS, versions, architectures, ...) of the hierarchical topology of modern architectures, includingNUMA memory nodes, sockets, shared caches, cores and simultaneous multithreading. It also gathers varioussystem attributes such as cache and memory information as well as the locality of I/O devices such asnetwork interfaces, InfiniBand HCAs or GPUs. It primarily aims at helping applications with gatheringinformation about modern computing hardware so as to exploit it accordingly and efficiently. - Homepage: http://www.open-mpi.org/projects/hwloc/
+
|The program gffread can be used to validate, filter, convert and perform various other operations on GFF files
 
|-
 
|-
|[http://icorn.sourceforge.net/documentation.html icorn]
+
|[http://rseqc.sourceforge.net/ RSeQC]
|0.97-IGB-gcc-4.9.4
+
|2.6.4-IGB-gcc-4.9.4-Python-2.7.13
|Inputs: Reference Sequence (FASTA) & reads (FASTQ) & information of short reads  
+
|RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. Some basic modules quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while RNA-seq specific modules evaluate sequencing saturation, mapped reads distribution, coverage uniformity, strand specificity, transcript level RNA integrity etc.
 
|-
 
|-
|[http://software.broadinstitute.org/software/igv/ igv]
+
|[https://github.com/ruanjue/smartdenovo SMARTdenovo]
|2.4.4-Java-1.8.0_152
+
|20170916-IGB-gcc-4.9.4-Perl-5.24.1
|The Integrative Genomics Viewer (IGV) is a high-performance visualization tool for interactive exploration of large, integrated genomic datasets. It supports a wide variety of data types, including array-based and next-generation sequence data, and genomic annotations.
+
|SMARTdenovo is a de novo assembler for PacBio and Oxford Nanopore (ONT) data. It produces an assembly from all-vs-all raw read alignments without an error correction stage. It also provides tools to generate accurate consensus sequences, though a platform dependent consensus polish tools (e.g. Quiver for PacBio or Nanopolish for ONT) are still required for higher accuracy.
 
|-
 
|-
|[https://mathgen.stats.ox.ac.uk/impute/impute_v2.html impute2]
+
|[http://fenderglass.github.io/Ragout/ Ragout]
|2.3.2
+
|2.0-IGB-gcc-4.9.4
|IMPUTE2 is freely available for academic use. To see rules for non-academic use, please read the LICENCE file, which is included with each software download.  
+
|Ragout (Reference-Assisted Genome Ordering UTility) is a tool for chromosome assembly using multiple references.
 +
|-
 +
|[https://www.pmgenomics.ca/hoffmanlab/proj/segway/ Segway]
 +
|2.0.1-IGB-gcc-4.9.4-Python-2.7.13
 +
|Segway is a tool for easy pattern discovery and identification in functional genomics data.
 +
|-
 +
|[http://jupyter.org/ jupyterlab]
 +
|0.34.10-IGB-gcc-4.9.4-Python-3.6.1
 +
|Project Jupyter exists to develop open-source software, open-standards, and services for interactive computing across dozens of programming languages.
 +
|-
 +
|[https://sourceforge.net/projects/phispy PhiSpy]
 +
|2.3-IGB-gcc-4.9.4-Python-2.7.13
 +
|A novel algorithm for finding prophages in microbial genomes that combines similarity-based and composition-based strategies
 
|-
 
|-
|[https://github.com/LLNL/ior ior]
+
|[http://www.gnu.org/software/ncurses/ ncurses]
|3.0.1-IGB-gcc-4.9.4
+
|.5.9-IGB-gcc-4.9.4<br>.6.0<br>.6.0-IGB-gcc-4.9.4
|Parallel filesystem I/O benchmark
+
|The Ncurses (new curses) library is a free software emulation of curses in System V Release 4.0, and more. It uses Terminfo format, supports pads and color and multiple highlights and forms characters and function-key mapping, and has all the other SYSV-curses enhancements over BSD Curses.
 
|-
 
|-
 
|[http://www.digip.org/jansson/ jansson]
 
|[http://www.digip.org/jansson/ jansson]
Line 1,365: Line 1,369:
 
|Jansson is a C library for encoding, decoding and manipulating JSON data.  
 
|Jansson is a C library for encoding, decoding and manipulating JSON data.  
 
|-
 
|-
|[http://www.canonware.com/jemalloc jemalloc]
+
|[http://bazel.io/ bazel]
|5.0.1-IGB-gcc-4.9.4
+
|0.6.0-Java-1.8.0_121
|jemalloc is a general purpose malloc(3) implementation that emphasizes fragmentation avoidance and scalable concurrency support.
+
|Bazel is a build tool that builds code quickly and reliably. It is used to build the majority of Googles software.
 
|-
 
|-
|[http://jupyter.org/ jupyter]
+
|[http://www.antlr2.org/ ANTLR]
|1.0.0-IGB-gcc-4.9.4-Python-3.6.1
+
|.2.7.7-IGB-gcc-4.9.4
|Project Jupyter exists to develop open-source software, open-standards, and services for interactive computing across dozens of programming languages.
+
|ANTLR, ANother Tool for Language Recognition, (formerly PCCTS) is a language tool that provides a framework for constructing recognizers, compilers, and translators from grammatical descriptions containing Java, C#, C++, or Python actions.
|-
 
|[http://jupyter.org/ jupyterlab]
 
|0.34.10-IGB-gcc-4.9.4-Python-3.6.1
 
|Project Jupyter exists to develop open-source software, open-standards, and services for interactive computing across dozens of programming languages.
 
 
|-
 
|-
|[http://pachterlab.github.io/kallisto/ kallisto]
+
|[http://www.htslib.org/ SAMtools]
|0.43.1-IGB-gcc-4.9.4<br>0.44.0-IGB-gcc-4.9.4
+
|0.1.20-IGB-gcc-4.9.4<br>1.4-IGB-gcc-4.9.4<br>1.4.1-IGB-gcc-4.9.4<br>1.5-IGB-gcc-4.9.4<br>1.7-IGB-gcc-4.9.4
|kallisto is a program for quantifying abundances of transcripts from RNA-Seq data, or more generally of target sequences using high-throughput sequencing reads.
+
|SAM Tools provide various utilities for manipulating alignments in the SAM format,  including sorting, merging, indexing and generating alignments in a per-position format.
 
|-
 
|-
|[http://genome.cse.ucsc.edu kentUtils]
+
|[https://github.com/Ensembl/ensembl-vep VEP]
|353-IGB-gcc-4.9.4
+
|92.4-IGB-gcc-4.9.4-Perl-5.24.1
|UCSC genome browser kent bioinformatic utilities
+
|VEP (Variant Effect Predictor) predicts the functional effects of genomic variants.
 
|-
 
|-
|[https://github.com/matthiasplappert/keras-rl keras-rl]
+
|[http://drive5.com/muscle/ MUSCLE]
|0.3.0-IGB-gcc-4.9.4-Python-2.7.13
+
|3.8.31-IGB-gcc-4.9.4
|keras-rl implements some state-of-the art deep reinforcement learning algorithms in Python and seamlessly integrates with the deep learning library Keras.  
+
|MUSCLE is one of the best-performing multiple alignment programs  according to published benchmark tests, with accuracy and speed that are consistently  better than CLUSTALW. MUSCLE can align hundreds of sequences in seconds. Most users  learn everything they need to know about MUSCLE in a few minutes—only a handful of  command-line options are needed to perform common alignment tasks. - Homepage: http://drive5.com/muscle/
 
|-
 
|-
|[https://github.com/alticelabs/kyoto kyoto]
+
|[https://github.com/TransDecoder/TransDecoder/wiki TransDecoder]
|.20170410-IGB-gcc-4.9.4<br>20170410-IGB-gcc-4.9.4
+
|5.1.0-IGB-gcc-4.9.4-Perl-5.24.1
|Kyoto Tycoon is a lightweight network server on top of the Kyoto Cabinet key-value database, built for high-performance and concurrency. Some of its features include:
+
|TransDecoder identifies candidate coding regions within transcript sequences, such as those generated by de novo RNA-Seq transcript assembly using Trinity, or constructed based on RNA-Seq alignments to the genome using Tophat and Cufflinks.
 
|-
 
|-
|[http://lbzip2.org/ lbzip2]
+
|[http://abacus.gene.ucl.ac.uk/software/paml.html PAML]
|2.5-IGB-gcc-4.9.4
+
|4.9e-IGB-gcc-4.9.4
|lbzip2 is a free, multi-threaded compression utility with support for bzip2 compressed file format.
+
|PAML is a package of programs for phylogenetic  analyses of DNA or protein sequences using maximum likelihood. - Homepage: http://abacus.gene.ucl.ac.uk/software/paml.html
 
|-
 
|-
|[https://lftp.yar.ru/ lftp]
+
|[http://www.cbs.dtu.dk/cgi-bin/sw_request?rnammer RNAmmer]
|4.8.3
+
|1.2-IGB-gcc-4.9.4-Perl-5.24.1
|FTP is a sophisticated file transfer program supporting a number of network protocols (ftp, http, sftp, fish, torrent).
+
|Ribosomal RNA sub units
 
|-
 
|-
|[http://apps.jcns.fz-juelich.de/doku/sc/libcerf libcerf]
+
|[http://ocaml.org/ OCaml]
|1.5-IGB-gcc-4.9.4
+
|4.05.0-IGB-gcc-4.9.4
|libcerf is a self-contained numeric library that provides an efficient and accurate implementation of complex error functions, along with Dawson, Faddeeva, and Voigt functions. - Homepage: http://apps.jcns.fz-juelich.de/doku/sc/libcerf
+
|OCaml is a general purpose industrial-strength programming language with an emphasis on expressiveness and safety. Developed for more than 20 years at Inria it benefits from one of the most advanced type systems and supports functional, imperative and object-oriented styles of programming.
 
|-
 
|-
|[http://opendap.org/download/libdap libdap]
+
|[http://eigen.tuxfamily.org/index.php?title=Main_Page Eigen]
|.3.19.1-IGB-gcc-4.9.4
+
|.3.3.3-IGB-gcc-4.9.4
|A C++ SDK which contains an implementation of DAP 2.0 and the development versions of DAP3, up to 3.4. This includes both Client- and Server-side support classes.
+
|Eigen is a C++ template library for linear algebra: matrices, vectors, numerical solvers, and related algorithms. - Homepage: http://eigen.tuxfamily.org/index.php?title=Main_Page
 
|-
 
|-
|[http://dri.freedesktop.org libdrm]
+
|[https://github.com/fchollet/keras Keras]
|.2.4.76-IGB-gcc-4.9.4
+
|2.0.6-IGB-gcc-4.9.4-Python-2.7.13<br>2.0.8-IGB-gcc-4.9.4-Python-3.6.1<br>2.1.2-IGB-gcc-4.9.4-Python-3.6.1<br>2.1.5-IGB-gcc-4.9.4-Python-3.6.1<br>2.2.0-IGB-gcc-4.9.4-Python-3.6.1
|Direct Rendering Manager runtime library.
+
|Keras is a high-level neural networks API, written in Python and capable of running on top of TensorFlow, CNTK, or Theano.  
 
|-
 
|-
|[http://libevent.org/ libevent]
+
|[https://pygraphviz.github.io/ pygraphviz]
|.2.1.8-IGB-gcc-4.9.4
+
|1.3.1-IGB-gcc-4.9.4-Python-3.6.1
|The libevent API provides a mechanism to execute a callback function when a specific event occurs on a file descriptor or after a timeout has been reached. Furthermore, libevent also support callbacks due to signals or regular timeouts. - Homepage: http://libevent.org/
+
|PyGraphviz is a Python interface to the Graphviz graph layout and visualization package. With PyGraphviz you can create, edit, read, write, and draw graphs using Python to access the Graphviz graph data structure and layout algorithms.
 
|-
 
|-
|[http://sourceware.org/libffi/ libffi]
+
|[https://github.com/nanoporetech/pomoxis pomoxis]
|.3.2.1-IGB-gcc-4.9.4
+
|0.1.0-IGB-gcc-4.9.4-Python-3.6.1
|The libffi library provides a portable, high level programming interface to various callingconventions. This allows a programmer to call any function specified by a call interface description at run-time. - Homepage: http://sourceware.org/libffi/
+
|Pomoxis contains a set of services to perform analysis of squiggles as they are produced in real-time along with fast pipelines for generating draft assemblies.
 
|-
 
|-
|[http://libgd.bitbucket.org/ libgd]
+
|[http://www.sanger.ac.uk/science/tools/reapr REAPR]
|.2.2.4-IGB-gcc-4.9.4
+
|1.0.18-IGB-gcc-4.9.4
|GD is an open source code library for the dynamic creation of images by programmers. - Homepage: http://libgd.bitbucket.org/
+
|REAPR is a tool that evaluates the accuracy of a genome assembly using mapped paired end reads, without the use of a reference genome for comparison. It can be used in any stage of an assembly pipeline to automatically break incorrect scaffolds and flag other errors in an assembly for manual inspection. It reports mis-assemblies and other warnings, and produces a new broken assembly based on the error calls. - Homepage: http://www.sanger.ac.uk/science/tools/reapr
 
|-
 
|-
|[http://deeplearning.net/software/libgpuarray/ libgpuarray]
+
|[https://github.com/pezmaster31/bamtools BamTools]
|0.6.5-IGB-gcc-4.9.4
+
|2.4.1-IGB-gcc-4.9.4
|Make a common GPU ndarray(n dimensions array) that can be reused by all projects that is as future proof as possible, while keeping it easy to use for simple need/quick test. - Homepage: http://deeplearning.net/software/libgpuarray/
+
|BamTools provides both a programmers API and an end-users toolkit for handling BAM files.
 
|-
 
|-
|[http://hannonlab.cshl.edu/fastx_toolkit/ libgtextutils]
+
|[https://ccl.northwestern.edu/netlogo/ NetLogo]
|.0.7-IGB-gcc-4.9.4
+
|5.2.1<br>6.0.3
|ligtextutils is a dependency of fastx-toolkit and is provided via the same upstream - Homepage: http://hannonlab.cshl.edu/fastx_toolkit/
+
|NetLogo is a multi-agent programmable modeling environment. It is used by many tens of thousands of students, teachers and researchers worldwide.
 
|-
 
|-
|[http://libharu.org/ libharu]
+
|[https://github.com/lilydjwg/pssh pssh]
|2.3.0-IGB-gcc-4.9.4
+
|2.3.1-IGB-gcc-4.9.4-Python-2.7.13
|libHaru is a free, cross platform, open source library for generating PDF files. - Homepage: http://libharu.org/
+
|PSSH provides parallel versions of OpenSSH and related tools, including pssh, pscp, prsync, pnuke and pslurp. This project includes psshlib which can be used within custom applications.
 
|-
 
|-
|[http://sourceforge.net/projects/libjpeg-turbo/ libjpeg-turbo]
+
|[https://github.com/alticelabs/kyoto kyoto]
|.1.5.1-IGB-gcc-4.9.4
+
|.20170410-IGB-gcc-4.9.4<br>20170410-IGB-gcc-4.9.4
|libjpeg-turbo is a fork of the original IJG libjpeg which uses SIMD to accelerate baseline JPEGcompression and decompression. libjpeg is a library that implements JPEG image encoding, decoding and transcoding. - Homepage: http://sourceforge.net/projects/libjpeg-turbo/
+
|Kyoto Tycoon is a lightweight network server on top of the Kyoto Cabinet key-value database, built for high-performance and concurrency. Some of its features include:
 
|-
 
|-
|[http://cgit.freedesktop.org/xorg/lib/libpciaccess/ libpciaccess]
+
|[https://github.com/nservant/HiC-Pro HiC-Pro]
|.0.13.4-IGB-gcc-4.9.4
+
|2.9.0-IGB-gcc-4.9.4-Python-2.7.13
|Generic PCI access library.
+
|HiC-Pro was designed to process Hi-C data, from raw fastq files (paired-end Illumina data) to the normalized contact maps. Since version 2.7.0, HiC-Pro supports the main Hi-C protocols, including digestion protocols as well as protocols that do not require restriction enzyme such as DNase Hi-C.
 
|-
 
|-
|[http://www.libpng.org/pub/png/libpng.html libpng]
+
|[https://github.com/DReichLab/EIG eigensoft]
|.1.6.29-IGB-gcc-4.9.4
+
|7.2.1-IGB-gcc-4.9.4
|libpng is the official PNG reference library - Homepage: http://www.libpng.org/pub/png/libpng.html
+
|The EIGENSOFT package combines functionality from our population genetics methods (Patterson et al. 2006) and our EIGENSTRAT stratification correction method (Price et al. 2006).  
 
|-
 
|-
|[http://xcb.freedesktop.org/ libpthread-stubs]
+
|[https://bitbucket.org/nygcresearch/treemix treemix]
|.0.3-IGB-gcc-4.9.4
+
|1.13-IGB-gcc-4.9.4
|The X protocol C-language Binding (XCB) is a replacement for Xlib featuring a small footprint,latency hiding, direct access to the protocol, improved threading support, and extensibility.
+
|TreeMix is a method for inferring the patterns of population splits and mixtures in the history of a set of populations. In the underlying model, the modern-day populations in a species are related to a common ancestor via a graph of ancestral populations. We use the allele frequencies in the modern populations to infer the structure of this graph.
 
|-
 
|-
|[http://cnswww.cns.cwru.edu/php/chet/readline/rltop.html libreadline]
+
|[http://www.bioperl.org/ BioPerl]
|.6.3-IGB-gcc-4.9.4
+
|1.7.1-IGB-gcc-4.9.4-Perl-5.24.1<br>1.7.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
|The GNU Readline library provides a set of functions for use by applications that allow users to edit command lines as they are typed in. Both Emacs and vi editing modes are available. The Readline library includes additional functions to maintain a list of previously-entered command lines, to recall and perhaps reedit those lines, and perform csh-like history expansion on previous commands. - Homepage: http://cnswww.cns.cwru.edu/php/chet/readline/rltop.html
+
|Bioperl is the product of a community effort to produce Perl code which is useful in biology. Examples include Sequence objects, Alignment objects and database searching objects.
 
|-
 
|-
|[http://doc.libsodium.org/ libsodium]
+
|[http://bio-bwa.sourceforge.net/ BWA]
|1.0.13-IGB-gcc-4.9.4
+
|0.5.9-IGB-gcc-4.9.4<br>0.6.2-IGB-gcc-4.9.4<br>0.7.15-IGB-gcc-4.9.4<br>0.7.17-IGB-gcc-4.9.4
|Sodium is a modern, easy-to-use software library for encryption, decryption, signatures, password hashing and more.
+
|Burrows-Wheeler Aligner (BWA) is an efficient program that aligns relatively short nucleotide sequences against a long reference sequence such as the human genome. - Homepage: http://bio-bwa.sourceforge.net/
 
|-
 
|-
|[http://www.gnu.org/software/libtool libtool]
+
|[http://ecogenomics.github.io/CheckM CheckM]
|.2.4.6<br>.2.4.6-IGB-gcc-4.9.4
+
|1.0.7-IGB-gcc-4.9.4-Python-2.7.13
|GNU libtool is a generic library support script. Libtool hides the complexity of using shared libraries behind a consistent, portable interface. - Homepage: http://www.gnu.org/software/libtool
+
|CheckM provides a set of tools for assessing the quality of genomes recovered from isolates, single cells, or metagenomes.
 
|-
 
|-
|[http://xmlsoft.org/ libxml2]
+
|[https://cran.r-project.org/web/packages/Rmpi/index.html Rmpi]
|2.9.4-IGB-gcc-4.9.4
+
|0.6-6-IGB-gcc-4.9.4-R-3.4.2
|Libxml2 is the XML C parser and toolchain developed for the Gnome project (but usable outside of the Gnome platform). - Homepage: http://xmlsoft.org/
+
|An interface (wrapper) to MPI APIs. It also provides interactive R manager and worker environment.
 
|-
 
|-
|[http://xmlsoft.org/ libxslt]
+
|[https://www.tug.org/texlive/ texlive]
|1.1.29-IGB-gcc-4.9.4
+
|20170520-IGB-gcc-4.9.4
|Libxslt is the XSLT C library developed for the GNOME project (but usable outside of the Gnome platform).
+
|TeX Live is an easy way to get up and running with the TeX document production system. It provides a comprehensive TeX system with binaries for most flavors of Unix, including GNU/Linux, and also Windows. It includes all the major TeX-related programs, macro packages, and fonts that are free software, including support for many languages around the world.  
 
|-
 
|-
|[http://support.10xgenomics.com/genome-exome/software/pipelines/latest/what-is-long-ranger longranger]
+
|[http://biom-format.org/ biom-format]
|2.1.3<br>2.1.6<br>2.2.2
+
|2.1.6-IGB-gcc-4.9.4-Python-2.7.13<br>2.1.6-IGB-gcc-4.9.4-Python-3.6.1
|Long Ranger is a set of analysis pipelines that processes Chromium sequencing output to align reads and call and phase SNPs, indels, and structural variants. There are five main pipelines, each triggered by a longranger command
+
|The BIOM file format (canonically pronounced biome) is designed to be a general-use format for representing biological sample by observation contingency tables.
 
|-
 
|-
|[https://support.10xgenomics.com/genome-exome/software/visualization/latest/what-is-loupe loupe]
+
|[http://www.graphviz.org/ graphviz]
|2.1.1
+
|2.40.1-IGB-gcc-4.9.4<br>2.40.1-IGB-gcc-4.9.4-Python-2.7.13
|Loupe is a genome browser designed to visualize the Linked-Read data produced by the 10x Chromium Platform. Loupe is named for a jewelers loupe, which is used to inspect gems.
+
|Graphviz is open source graph visualization software. Graph visualization is a way of representing structural information as diagrams of abstract graphs and networks. It has important applications in networking, bioinformatics,  software engineering, database and web design, machine learning, and in visual interfaces for other technical domains.
 
|-
 
|-
|[http://www.oberhumer.com/opensource/lzo/ lzo]
+
|[https://github.com/IGBIllinois/biodatabase/ biodatabase]
|.2.10-IGB-gcc-4.9.4
+
|1.0-IGB-gcc-4.9.4
|Portable lossless data compression library
+
|Scripts to create databases on the biodatabase machine.
 
|-
 
|-
|[https://github.com/DpeerLab/magic magic]
+
|[https://github.com/pjeraldo/imtornado2 IM-TORNADO]
|0.1-IGB-gcc-4.9.4-Python-3.6.1
+
|2.0.3.3-IGB-gcc-4.9.4-Python-2.7.13
|A diffusion-based imputation method reveals gene-gene interactions in single-cell RNA-sequencing data
+
|A pipeline for 16S reads from paired-end libraries
 
|-
 
|-
|[https://github.com/ginolhac/mapDamage mapDamage]
+
|[https://www.ncbi.nlm.nih.gov/genbank/tbl2asn2/ tbl2asn]
|2.0.5-IGB-gcc-4.9.4-Python-2.7.13
+
|20180516
|mapDamage2 is a computational framework written in Python and R, which tracks and quantifies DNA damage patterns among ancient DNA sequencing reads generated by Next-Generation Sequencing platforms.
+
|Tbl2asn is a command-line program that automates the creation of sequence records for submission to GenBank
 
|-
 
|-
|[https://github.com/nanoporetech/medaka medaka]
+
|[http://www.darwinsys.com/file/ file]
|0.1.0-IGB-gcc-4.9.4-Python-3.6.1
+
|.5.30-IGB-gcc-4.9.4
|Medaka demonstrates a framework for error correcting sequencing data, particularly aimed at nanopore sequencing. Tools are provided for both training and inference. The code exploits the keras deep learning library.
+
|The file command is a file type guesser, that is, a command-line tool that tells you in words what kind of data a file contains.
 
|-
 
|-
|[https://github.com/IGBIllinois/memprof memprof]
+
|[http://ant.apache.org/ ant]
|1.0
+
|1.10.1-Java-1.8.0_121
|HPC Cluster Memory Profiling
+
|Apache Ant is a Java library and command-line tool whose mission is to drive processes described in build files as targets and extension points dependent upon each other. The main known usage of Ant is the build of Java applications. - Homepage: http://ant.apache.org/
 
|-
 
|-
|[https://bitbucket.org/biobakery/metaphlan2 metaphlan2]
+
|[http://eddylab.org/software.html squid]
|2.6.0-IGB-gcc-4.9.4-Python-3.6.1<br>2.7.6-IGB-gcc-4.9.4-Python-2.7.13
+
|1.9g-IGB-gcc-4.9.4
|MetaPhlAn is a computational tool for profiling the composition of microbial communities (Bacteria, Archaea, Eukaryotes and Viruses) from metagenomic shotgun sequencing data (i.e. not 16S) with species-level. With the newly added StrainPhlAn module, it is now possible to perform accurate strain-level microbial profiling.
+
|A C library that is bundled with much of the above software. C function library for sequence analysis.
 
|-
 
|-
|[https://github.com/LangilleLab/microbiome_helper microbiome_helper]
+
|[https://github.com/lh3/minimap minimap]
|20171114-IGB-gcc-4.9.4
+
|0.2-IGB-gcc-4.9.4<br>2.11-IGB-gcc-4.9.4<br>2.3-IGB-gcc-4.9.4<br>2.8-IGB-gcc-4.9.4
|An assortment of scripts to help process and automate various microbiome and metagenomic bioinformatic tools. We provide workflows, tutorials and a virtual box image to help researchers process microbial data.
+
|Minimap is an experimental tool to efficiently find multiple approximate mapping positions between two sets of long sequences, such as between reads and reference genomes, between genomes and between long noisy reads.  
 
|-
 
|-
|[http://microbiomeutil.sourceforge.net/ microbiomeutil]
+
|[https://melodi.ee.washington.edu/gmtk/ GMTK]
|20110519-IGB-gcc-4.9.4
+
|1.4.4-IGB-gcc-4.9.4
|Contains ChimeraSlayer, WigeoN, and NAST-iEr
+
|The Graphical Models Toolkit (GMTK) is an open source, publicly available toolkit for rapidly prototyping statistical models using dynamic graphical models (DGMs) and dynamic Bayesian networks (DBNs). GMTK can be used for applications and research in speech and language processing, bioinformatics, activity recognition, and any time series application. GMTK has many features, including exact and approximate inference; a large variety of built-in factors including dense, sparse, and deterministic conditional probability tables, native support for ARPA backoff-based factors and factored language models, parameter sharing, gamma and beta distributions, dense and sparse Gaussian factors, heterogeneous mixtures, deep neural network factors, and time-inhomogeneous trellis factors; arbitrary order embedded Markov chains; a GUI-based graph viewer; flexible feature-file support and processing tools (supporting pfiles, HTK files, ASCII/binary, and HDF5 files); and both offline and streaming online inference methods that can be used for both parameter learning and prediction. More information is available in the documentation. All in all, GMTK offers a flexible, concise, and expressive probabilistic modeling framework with which one may rapidly specify a vast collection of temporal statistical models.
 
|-
 
|-
|[https://github.com/lh3/miniasm miniasm]
+
|[http://python.org/ Python]
|0.2-IGB-gcc-4.9.4
+
|2.7.13-IGB-gcc-4.9.4<br>3.6.1-IGB-gcc-4.9.4
|Miniasm is a very fast OLC-based de novo assembler for noisy long reads. It takes all-vs-all read self-mappings (typically by minimap) as input and outputs an assembly graph in the GFA format. Different from mainstream assemblers, miniasm does not have a consensus step. It simply concatenates pieces of read sequences to generate the final unitig sequences. Thus the per-base error rate is similar to the raw input reads.
+
|Python is a programming language that lets you work more quickly and integrate your systems more effectively.
 
|-
 
|-
|[https://github.com/lh3/minimap minimap]
+
|[http://lowelab.ucsc.edu/tRNAscan-SE/ tRNAscan-SE]
|0.2-IGB-gcc-4.9.4<br>2.11-IGB-gcc-4.9.4<br>2.3-IGB-gcc-4.9.4<br>2.8-IGB-gcc-4.9.4
+
|1.3.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
|Minimap is an experimental tool to efficiently find multiple approximate mapping positions between two sets of long sequences, such as between reads and reference genomes, between genomes and between long noisy reads.
+
|tRNAscan-SE: a tool for finding transfer RNAs
 
|-
 
|-
|[https://github.com/PacificBiosciences/minorseq/blob/54ac795d7c119d21a4611d91ac458cd3e2e2b30a/doc/INSTALL.md minorseq]
+
|[http://www.biopython.org Biopython]
|20180314-IGB-gcc-4.9.4
+
|1.68-IGB-gcc-4.9.4-Python-2.7.13<br>1.68-IGB-gcc-4.9.4-Python-3.6.1
|Minor Variant Calling and Phasing Tools
+
|Biopython is a set of freely available tools for biological computation writtenin Python by an international team of developers. It is a distributed collaborative effort todevelop Python libraries and applications which address the needs of current and future work inbioinformatics.  - Homepage: http://www.biopython.org
 
|-
 
|-
|[https://www.mdc-berlin.de/8551903/en/ mirdeep]
+
|[https://mathema.tician.de/software/pycuda/ PyCUDA]
|2.0.0.8-IGB-gcc-4.9.4
+
|2017.1-IGB-gcc-4.9.4-Python-2.7.13
|miRDeep2 is a completely overhauled tool which discovers microRNA genes by analyzing sequenced RNAs.  
+
|PyCUDA lets you access Nvidia‘s CUDA parallel computation API from Python. - Homepage: https://mathema.tician.de/software/pycuda/
 
|-
 
|-
|[https://github.com/jts/nanopolish nanopolish]
+
|[http://libharu.org/ libharu]
|0.10.1-IGB-gcc-4.9.4<br>0.6.0-IGB-gcc-4.9.4<br>0.7.1-IGB-gcc-4.9.4<br>0.7.1-IGB-gcc-4.9.4-159d92b<br>0.8.3-IGB-gcc-4.9.4<br>0.8.5-IGB-gcc-4.9.4<br>0.9.0-IGB-gcc-4.9.4
+
|2.3.0-IGB-gcc-4.9.4
|Software package for signal-level analysis of Oxford Nanopore sequencing data.
+
|libHaru is a free, cross platform, open source library for generating PDF files. - Homepage: http://libharu.org/
 
|-
 
|-
|[https://github.com/ncbi/ncbi-vdb ncbi-vdb]
+
|[https://github.com/bioinf/Sibelia Sibelia]
|2.8.2-IGB-gcc-4.9.4
+
|3.0.7-IGB-gcc-4.9.4
|The SRA Toolkit and SDK from NCBI is a collection of tools and libraries for using data in the INSDC Sequence Read Archives. - Homepage: https://github.com/ncbi/ncbi-vdb
+
|Sibelia is a tool for finding synteny blocks in closely related genomes, like different strains of the same bacterial species.
 
|-
 
|-
|[http://cran.r-project.org/web/packages/ncdf4 ncdf4]
+
|shortbred/diamond
|1.16-IGB-gcc-4.9.4-R-3.3.3
+
|diamond/beta<br>diamond/devlocal
|This package provides a high-level R interface to data files written using Unidatas netCDF library (version 4 or earlier), which are binary data files that are portable across platforms and include metadata information in addition to the data sets.
+
|
 
|-
 
|-
|[http://www.gnu.org/software/ncurses/ ncurses]
+
|[https://www.continuum.io/anaconda-overview Anaconda3]
|.5.9-IGB-gcc-4.9.4<br>.6.0<br>.6.0-IGB-gcc-4.9.4
+
|5.0.1<br>5.1.0
|The Ncurses (new curses) library is a free software emulation of curses in System V Release 4.0, and more. It uses Terminfo format, supports pads and color and multiple highlights and forms characters and function-key mapping, and has all the other SYSV-curses enhancements over BSD Curses.
+
|Built to complement the rich, open source Python community,the Anaconda platform provides an enterprise-ready data analytics platform that empowers companies to adopt a modern open data science analytics architecture.
 
|-
 
|-
|[http://www.unidata.ucar.edu/software/netcdf/ netCDF]
+
|[http://www.lua.org/ Lua]
|.4.4.1.1-IGB-gcc-4.9.4<br>4.4.1.1-IGB-gcc-4.9.4
+
|5.1.5-IGB-gcc-4.9.4<br>5.3.4-IGB-gcc-4.9.4
|NetCDF (network Common Data Form) is a set of software libraries  and machine-independent data formats that support the creation, access, and sharing of array-oriented  scientific data. - Homepage: http://www.unidata.ucar.edu/software/netcdf/
+
|Lua is a powerful, fast, lightweight, embeddable scripting language. Lua combines simple procedural syntax with powerful data description constructs based on associative arrays and extensible semantics. Lua is dynamically typed, runs by interpreting bytecode for a register-based virtual machine, and has automatic memory management with incremental garbage collection, making it ideal for configuration, scripting, and rapid prototyping.
 
|-
 
|-
|[http://www.unidata.ucar.edu/software/netcdf/ netCDF-Fortran]
+
|[http://snver.sourceforge.net/ SNVer]
|.4.4.1-IGB-gcc-4.9.4<br>4.4.1-IGB-gcc-4.9.4
+
|0.5.3-Java-1.8.0_121
|NetCDF (network Common Data Form) is a set of software libraries and machine-independent data formats that support the creation, access, and sharing of array-oriented scientific data.
+
|SNVer is a statistical tool for calling common and rare variants in analysis of pool or individual next-generation sequencing data. It reports one single overall p-value for evaluating the significance of a candidate locus being a variant, based on which multiplicity control can be obtained.  
 
|-
 
|-
|[http://www.lysator.liu.se/~nisse/nettle/ nettle]
+
|[https://www.ruby-lang.org Ruby]
|3.3-IGB-gcc-4.9.4
+
|2.4.2-IGB-gcc-4.9.4
|Nettle is a cryptographic library that is designed to fit easily in more or less any context: In crypto toolkits for object-oriented languages (C++, Python, Pike, ...), in applications like LSH or GNUPG, or even in kernel space.
+
|Ruby is a dynamic, open source programming language with  a focus on simplicity and productivity. It has an elegant syntax that is natural to read and easy to write.
 
|-
 
|-
|[https://www.nextflow.io/ nextflow]
+
|[https://web.stanford.edu/group/pritchardlab/structure.html structure]
|0.25.7-Java-1.8.0_121<br>0.26.3-Java-1.8.0_152
+
|2.3.4-IGB-gcc-4.9.4
|Nextflow enables scalable and reproducible scientific workflows using software containers. It allows the adaptation of pipelines written in the most common scripting languages.  
+
|The program structure is a free software package for using multi-locus genotype data to investigate population structure.
 
|-
 
|-
|[https://ninja-build.org/ ninja]
+
|[http://metagene.nig.ac.jp/ MetaGeneAnnotator]
|1.8.2-IGB-gcc-4.9.4
+
|20080819-x86-64
|Ninja is a small build system with a focus on speed. It differs from other build systems in two major respects: it is designed to have its input files generated by a higher-level build system, and it is designed to run builds as fast as possible.
+
|MetaGeneAnnotator is a gene-finding program for prokaryote and phage.
 
|-
 
|-
|[http://nodejs.org nodejs]
+
|[https://github.com/lh3/miniasm miniasm]
|9.9.0-IGB-gcc-4.9.4
+
|0.2-IGB-gcc-4.9.4
|Node.js is a platform built on Chromes JavaScript runtime  for easily building fast, scalable network applications. Node.js uses an  event-driven, non-blocking I/O model that makes it lightweight and efficient, perfect for data-intensive real-time applications that run across distributed devices.
+
|Miniasm is a very fast OLC-based de novo assembler for noisy long reads. It takes all-vs-all read self-mappings (typically by minimap) as input and outputs an assembly graph in the GFA format. Different from mainstream assemblers, miniasm does not have a consensus step. It simply concatenates pieces of read sequences to generate the final unitig sequences. Thus the per-base error rate is similar to the raw input reads.
 
|-
 
|-
|[http://github.com/wolever/nose-parameterized nose-parameterized]
+
|[https://sourceforge.net/projects/rdp-classifier RDPClassifier]
|0.6.0-IGB-gcc-4.9.4-Python-2.7.13
+
|2.12-Java-1.8.0_152<br>2.2-Java-1.8.0_152
|Parameterized testing with any Python test framework.
+
|The RDP Classifier is a naive Bayesian classifier which was developed to provide rapid taxonomic placement based on rRNA sequence data. The RDP Classifier can rapidly and accurately classify bacterial and archaeal 16s rRNA sequences, and Fungal LSU sequences. It provides taxonomic assignments from domain to genus, with confidence estimates for each assignment.
 
|-
 
|-
|[http://www.novocraft.com/ novocraft]
+
|[http://454.com/products/analysis-software/index.asp 454]
|3.08.00
+
|2.8
|Powerful tool designed for mapping of short reads onto a reference genome from Illumina, Ion Torrent, and 454 NGS platforms.
+
|The GS Data Analysis Software package includes the tools to investigate complex genomic variation in samples including de novo assembly, reference guided alignment and variant calling, and low abundance variant identification and quantification. - Homepage:  http://454.com/products/analysis-software/index.asp
 
|-
 
|-
|[http://oss.sgi.com/projects/libnuma/ numactl]
+
|[https://github.com/IGBIllinois/memprof memprof]
|.2.0.11-GCC-4.9.4-2.28
+
|1.0
|The numactl program allows you to run your application program on specific cpus and memory nodes.It does this by supplying a NUMA memory policy to the operating system before running your program.The libnuma library provides convenient ways for you to add NUMA memory policies into your own program. - Homepage: http://oss.sgi.com/projects/libnuma/
+
|HPC Cluster Memory Profiling
 
|-
 
|-
|[http://numba.pydata.org/ numba]
+
|[http://qualimap.bioinfo.cipf.es/ qualimap]
|0.34.0-IGB-gcc-4.9.4-Python-2.7.13<br>0.34.0-IGB-gcc-4.9.4-Python-3.6.1
+
|2.2.1-Java-1.8.0_121
|Numba is an Open Source NumPy-aware optimizing compiler for Python sponsored by Continuum Analytics, Inc. It uses the remarkable LLVM compiler infrastructure to compile Python syntax to machine code.
+
|Qualimap 2 is a platform-independent application written in Java and R that provides both a Graphical User Inteface (GUI) and a command-line interface to facilitate the quality control of alignment sequencing data and its derivatives like feature counts.  
 
|-
 
|-
|[http://www.numpy.org numpy]
+
|[http://www.yandell-lab.org/software/maker.html MAKER]
|1.14.1-IGB-gcc-4.9.4-Python-3.6.1
+
|2.31.9-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded<br>3.00.0-beta-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded<br>3.01.1-beta-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
|NumPy is the fundamental package for scientific computing with Python. It contains among other things: a powerful N-dimensional array object, sophisticated (broadcasting) functions, tools for integrating C/C++ and Fortran code, useful linear algebra, Fourier transform, and random number capabilities. Besides its obvious scientific uses, NumPy can also be used as an efficient multi-dimensional container of generic data. Arbitrary data-types can be defined. This allows NumPy to seamlessly and speedily integrate with a wide variety of databases.
+
|MAKER is a portable and easily configurable genome annotation pipeline. Its purpose is to allow smaller eukaryotic and prokaryotic genome projects to independently annotate their genomes and to create genome databases. MAKER identifies repeats, aligns ESTs and proteins to a genome, produces ab-initio gene predictions and automatically synthesizes these data into gene annotations having evidence-based quality values. MAKER is also easily trainable: outputs of preliminary runs can be used to automatically retrain its gene prediction algorithm, producing higher quality gene-models on seusequent runs. MAKERs inputs are minimal and its ouputs can be directly loaded into a GMOD database. They can also be viewed in the Apollo genome browser; this feature of MAKER provides an easy means to annotate, view and edit individual contigs and BACs without the overhead of a database. MAKER should prove especially useful for emerging model organism projects with minimal bioinformatics expertise and computer resources.
 
|-
 
|-
|[http://www.bork.embl.de/pal2nal/ pal2nal]
+
|[https://github.com/DpeerLab/magic magic]
|14-IGB-gcc-4.9.4
+
|0.1-IGB-gcc-4.9.4-Python-3.6.1
|PAL2NAL is a program that converts a multiple sequence alignment of proteins and the corresponding DNA (or mRNA) sequences into a codon alignment.
+
|A diffusion-based imputation method reveals gene-gene interactions in single-cell RNA-sequencing data
 
|-
 
|-
|[http://pandoc.org pandoc]
+
|[https://github.com/alexdobin/STAR STAR]
|2.2.3.2
+
|2.5.3a-IGB-gcc-4.9.4<br>2.6.0c-IGB-gcc-4.9.4<br>2.6.1b-IGB-gcc-4.9.4
|If you need to convert files from one markup format into another, pandoc is your swiss-army knife
+
|STAR aligns RNA-seq reads to a reference genome using uncompressed suffix arrays.
 
|-
 
|-
|[https://www.gnu.org/software/parallel/ parallel]
+
|[http://nucleoatac.readthedocs.io/en/latest/ NucleoATAC]
|20170622-IGB-gcc-4.9.4
+
|0.3.4-IGB-gcc-4.9.4-Python-2.7.13
|parallel: GNU parallel is a shell tool for executing jobs in parallel using one or more computers.  
+
|NucleoATAC is a python package for calling nucleosome positions and occupancy using ATAC-Seq data. Functions for calling nucleosomes are included in the nucleoatac command-line function. NucleoATAC also includes other utlities for working with ATAC-seq data under the pyatac function.
 
|-
 
|-
|[http://compression.ca/pbzip2/ pbzip2]
+
|[https://git-lfs.github.com/ git-lfs]
|1.1.13-IGB-gcc-4.9.4
+
|2.2.1-IGB-gcc-4.9.4
|PBZIP2 is a parallel implementation of the bzip2 block-sorting file compressor that uses pthreads and achieves near-linear speedup on SMP machines.
+
|Git Large File Storage (LFS) replaces large files such as audio samples, videos,  datasets, and graphics with text pointers inside Git, while storing the file contents on a remote server  like GitHub.com or GitHub Enterprise.
 
|-
 
|-
|[http://perfsuite.ncsa.illinois.edu/ perfsuite]
+
|[https://cran.r-project.org/web/packages/h2o/index.html h2o]
|1.1.4-IGB-gcc-4.9.4
+
|3.14.0.3-IGB-gcc-4.9.4-R-3.3.3
|PerfSuite is a collection of tools, utilities, and libraries for software performance analysis where the primary design goals are ease of use, comprehensibility, interoperability, and simplicity. This software can provide a good "entry point" for more detailed performance analysis and can help point the way towards selecting other tools and/or techniques using more specialized software if necessary (for example, tools/libraries from academic research groups or third-party commercial software).  
+
|R scripting functionality for H2O, the open source math engine for big data that computes parallel distributed machine learning algorithms such as generalized linear models, gradient boosting machines, random forests, and neural networks (deep learning) within various cluster environments.
 
|-
 
|-
|[ftp://ftp.ebi.ac.uk/pub/databases/Pfam/Tools/README pfamscan]
+
|[https://github.com/data61/gossamer gossamer]
|1.6-IGB-gcc-4.9.4-Perl-5.24.1
+
|20170105-IGB-gcc-4.9.4
|This readme should help you get started with "pfam_scan.pl", which is for usewith the HMMER3 version of HMMER.
+
|The gossamer bioinformatics suite contains goss, gossple, xenome, and electus
 
|-
 
|-
|[https://github.com/pgmpy/pgmpy pgmpy]
+
|[https://support.10xgenomics.com/de-novo-assembly/software/overview/latest/welcome Supernova]
|20180320-IGB-gcc-4.9.4-Python-3.6.1
+
|1.1.5<br>1.2.0<br>1.2.1<br>2.0.0<br>2.0.1<br>2.1.0<br>2.1.1
|pgmpy is a python library for working with Probabilistic Graphical Models.
+
|Supernova is a software package for de novo assembly from Chromium Linked-Reads that are made from a single whole-genome library from an individual DNA source. A key feature of Supernova is that it creates diploid assemblies, thus separately representing maternal and paternal chromosomes over very long distances.
 
|-
 
|-
|[http://broadinstitute.github.io/picard/ picard]
+
|[(none) gompi]
|2.10.1-Java-1.8.0_121<br>2.10.1-Java-1.8.0_152<br>2.9.0-Java-1.8.0_121<br>2.9.4-Java-1.8.0_121
+
|.4.9.4
|A set of tools (in Java) for working with next generation sequencing data in the BAM  (http://samtools.github.io/hts-specs) format.
+
|GNU Compiler Collection (GCC) based compiler toolchain, including OpenMPI for MPI support. - Homepage: (none)
 
|-
 
|-
|[http://zlib.net/pigz/ pigz]
+
|[http://gcc.gnu.org/ GCCcore]
|2.3.4-IGB-gcc-4.9.4
+
|.4.9.4<br>.7.3.0
|pigz, which stands for parallel implementation of gzip, is a fully  functional replacement for gzip that exploits multiple processors and multiple cores  to the hilt when compressing data. pigz was written by Mark Adler, and uses the zlib  and pthread libraries.  - Homepage: http://zlib.net/pigz/
+
|The GNU Compiler Collection includes front ends for C, C++, Objective-C, Fortran, Java, and Ada, as well as libraries for these languages (libstdc++, libgcj,...). - Homepage: http://gcc.gnu.org/
|-
 
|[https://github.com/broadinstitute/pilon pilon]
 
|1.22-Java-1.8.0_121
 
|Pilon is a software tool which can be used to:- Automatically improve draft assemblies- Find variation among strains, including large event detection
 
|-
 
|[http://www.pixman.org/ pixman]
 
|0.34.0-IGB-gcc-4.9.4
 
|Pixman is a low-level software library for pixel manipulation, providing features such as imagecompositing and trapezoid rasterization. Important users of pixman are the cairo graphics library and the X server. - Homepage: http://www.pixman.org/
 
|-
 
|[http://www.freedesktop.org/wiki/Software/pkg-config/ pkg-config]
 
|.0.29.2-IGB-gcc-4.9.4
 
|pkg-config is a helper tool used when compiling applications and libraries. It helps you insert the correct compiler options on the command line so an application can use  gcc -o test test.c `pkg-config --libs --cflags glib-2.0` for instance, rather than hard-coding values on where to find glib (or other libraries). - Homepage: http://www.freedesktop.org/wiki/Software/pkg-config/
 
 
|-
 
|-
 
|[https://www.cog-genomics.org/plink2 plink]
 
|[https://www.cog-genomics.org/plink2 plink]
Line 1,641: Line 1,629:
 
|This is a comprehensive update to Shaun Purcells PLINK command-line program, developed by Christopher Chang with support from the NIH-NIDDKs Laboratory of Biological Modeling, the Purcell Lab at Mount Sinai School of Medicine, and others.  
 
|This is a comprehensive update to Shaun Purcells PLINK command-line program, developed by Christopher Chang with support from the NIH-NIDDKs Laboratory of Biological Modeling, the Purcell Lab at Mount Sinai School of Medicine, and others.  
 
|-
 
|-
|[https://github.com/nanoporetech/pomoxis pomoxis]
+
|[http://www.mpich.org/ MPICH]
|0.1.0-IGB-gcc-4.9.4-Python-3.6.1
+
|3.0.4-GCC-4.9.4-2.28
|Pomoxis contains a set of services to perform analysis of squiggles as they are produced in real-time along with fast pipelines for generating draft assemblies.
+
|MPICH v3.x is an open source high-performance MPI 3.0 implementation.It does not support InfiniBand (use MVAPICH2 with InfiniBand devices).
 
|-
 
|-
|[https://github.com/arq5x/poretools poretools]
+
|[https://github.com/BSSeeker/BSseeker2 BS-Seeker]
|0.6.0-IGB-gcc-4.9.4-Python-2.7.13
+
|2.1.2-IGB-gcc-4.9.4-Python-2.7.13
|a toolkit for working with nanopore sequencing data from Oxford Nanopore. - Homepage: https://github.com/arq5x/poretools
+
|BS Seeker 2 is a seamless and versatile pipeline for accurately and fast mapping the bisulfite-treated short reads. - Homepage: https://github.com/BSSeeker/BSseeker2
 
|-
 
|-
|[http://matsen.fhcrc.org/pplacer/ pplacer]
+
|[http://www.unidata.ucar.edu/software/netcdf/ netCDF]
|1.1.alpha19
+
|.4.4.1.1-IGB-gcc-4.9.4<br>4.4.1.1-IGB-gcc-4.9.4
|Pplacer places query sequences on a fixed reference phylogenetic tree to maximize phylogenetic likelihood or posterior probability according to a reference alignment. Pplacer is designed to be fast, to give useful information about uncertainty, and to offer advanced visualization and downstream analysis.
+
|NetCDF (network Common Data Form) is a set of software libraries  and machine-independent data formats that support the creation, access, and sharing of array-oriented  scientific data. - Homepage: http://www.unidata.ucar.edu/software/netcdf/
 
|-
 
|-
|[http://www.primer3.org primer3]
+
|[http://xmlsoft.org/ libxslt]
|2.4.0-IGB-gcc-4.9.4
+
|1.1.29-IGB-gcc-4.9.4
|Primer3 is a widely used program for designing PCR primers (PCR = "Polymerase Chain Reaction"). PCR is an essential and ubiquitous tool in genetics and molecular biology. Primer3 can also design hybridization probes and sequencing primers.  
+
|Libxslt is the XSLT C library developed for the GNOME project (but usable outside of the Gnome platform).
 
|-
 
|-
|[https://github.com/tseemann/prokka prokka]
+
|[https://github.com/ComparativeGenomicsToolkit/cactus cactus]
|1.12-IGB-gcc-4.9.4-Perl-5.24.1<br>1.13-IGB-gcc-4.9.4-Perl-5.24.1
+
|20180705-IGB-gcc-4.9.4-Python-2.7.13
|Whole genome annotation is the process of identifying features of interest in a set of genomic DNA sequences, and labelling them with useful information. Prokka is a software tool to annotate bacterial, archaeal and viral genomes quickly and produce standards-compliant output files.
+
|Cactus is a reference-free whole-genome multiple alignment program.
 
|-
 
|-
|[https://github.com/google/protobuf protobuf]
+
|[https://github.com/COMBINE-lab/salmon Salmon]
|2.6.1-IGB-gcc-4.9.4<br>3.5.0-IGB-gcc-4.9.4
+
|0.11.3-IGB-gcc-4.9.4<br>0.8.2-IGB-gcc-4.9.4-Python-2.7.13<br>0.9.1-IGB-gcc-4.9.4
|Protocol Buffers (a.k.a., protobuf) are Googles language-neutral, platform-neutral, extensible mechanism for serializing structured data.
+
|Salmon is a wicked-fast program to produce a highly-accurate, transcript-level quantification estimates from RNA-seq data.
 
|-
 
|-
|[https://github.com/lilydjwg/pssh pssh]
+
|[http://www.bx.psu.edu/~rsharris/lastz/ LASTZ]
|2.3.1-IGB-gcc-4.9.4-Python-2.7.13
+
|1.04.00-IGB-gcc-4.9.4
|PSSH provides parallel versions of OpenSSH and related tools, including pssh, pscp, prsync, pnuke and pslurp. This project includes psshlib which can be used within custom applications.
+
|LASTZ is a program for aligning DNA sequences, a pairwise aligner. Originally designed to handle sequences the size of human chromosomes and from different species, it is also useful for sequences produced by NGS  sequencing technologies such as Roche 454. - Homepage: http://www.bx.psu.edu/~rsharris/lastz/
 
|-
 
|-
|[https://daler.github.io/pybedtools/main.html pybedtools]
+
|[http://www.drive5.com/usearch/index.html USEARCH]
|0.7.10-IGB-gcc-4.9.4-Python-3.6.1
+
|6.1.544<br>7.0.1090<br>9.2.64
|pybedtools is a Python package that wraps BEDTools, so you will need both installed.
+
|USEARCH is a unique sequence analysis tool which offers search and clustering algorithms that are often orders of magnitude faster than BLAST.
 
|-
 
|-
|[http://deeplearning.net/software/libgpuarray pygpu]
+
|[http://www.mathworks.com/products/matlab MATLAB]
|0.6.5-IGB-gcc-4.9.4-Python-2.7.13
+
|2017a<br>2017b
|Python bindings for libgpuarray - Homepage: http://deeplearning.net/software/libgpuarray
+
|MATLAB is a high-level language and interactive environment that enables you to perform computationally intensive tasks faster than with traditional programming languages such as C, C++, and Fortran.
 
|-
 
|-
|[https://pygraphviz.github.io/ pygraphviz]
+
|[https://github.com/DecodeGenetics/graphtyper graphtyper]
|1.3.1-IGB-gcc-4.9.4-Python-3.6.1
+
|1.3-IGB-gcc-4.9.4
|PyGraphviz is a Python interface to the Graphviz graph layout and visualization package. With PyGraphviz you can create, edit, read, write, and draw graphs using Python to access the Graphviz graph data structure and layout algorithms.
+
|Graphtyper is a highly scalable genotyping software. It represents a reference genome and known variants of a genomic region using an acyclic mathematical graph structure (a "pangenome reference"), which high-throughput sequence reads are re-aligned to for the purpose of discovering and genotyping SNPs and small indels.
 
|-
 
|-
|[https://github.com/lisa-lab/pylearn2 pylearn2]
+
|[http://www.sanger.ac.uk/science/tools/ssaha2-0 ssaha2]
|20170525-IGB-gcc-4.9.4-Python-2.7.13
+
|2.5.5-IGB-gcc-4.9.4
|Pylearn2 is a library designed to make machine learning research easy. - Homepage: https://github.com/lisa-lab/pylearn2
+
|SSAHA2 (Sequence Search and Alignment by Hashing Algorithm) is a pairwise sequence alignment program designed for the efficient mapping of sequencing reads onto genomic reference sequences.
 
|-
 
|-
|[http://qualimap.bioinfo.cipf.es/ qualimap]
+
|[https://github.com/magnusmanske/snpomatic snpomatic]
|2.2.1-Java-1.8.0_121
+
|1.0-IGB-gcc-4.9.4
|Qualimap 2 is a platform-independent application written in Java and R that provides both a Graphical User Inteface (GUI) and a command-line interface to facilitate the quality control of alignment sequencing data and its derivatives like feature counts.  
+
|SNP-o-matic is a fast, stringent short-read mapping software. It supports a multitude of output types and formats, for uses in filtering reads, alignments, sequence-based genotyping calls, assisted reassembly of contigs etc.
 
|-
 
|-
|[https://sourceforge.net/projects/quast/ quast]
+
|[http://www.nwchem-sw.org NWChem]
 +
|6.6.revision27746-IGB-gcc-4.9.4-Python-2.7.13
 +
|NWChem aims to provide its users with computational chemistry tools that are scalable both in their ability to treat large scientific computational chemistry problems efficiently, and in their use of available parallel computing resources from high-performance parallel supercomputers to conventional workstation clusters. NWChem software can handle: biomolecules, nanostructures, and solid-state; from quantum to classical, and all combinations; Gaussian basis functions or plane-waves; scaling from one to thousands of processors; properties and relativity.
 +
|-
 +
|[https://sourceforge.net/projects/quast/ quast]
 
|4.6.1-IGB-gcc-4.9.4-Python-2.7.13<br>5.0.0-IGB-gcc-4.9.4-Python-3.6.1
 
|4.6.1-IGB-gcc-4.9.4-Python-2.7.13<br>5.0.0-IGB-gcc-4.9.4-Python-3.6.1
 
|QUAST performs fast and convenient quality evaluation and comparison of genome assemblies.  
 
|QUAST performs fast and convenient quality evaluation and comparison of genome assemblies.  
 
|-
 
|-
|[https://github.com/mahulchak/quickmerge quickmerge]
+
|[http://support.10xgenomics.com/genome-exome/software/pipelines/latest/what-is-long-ranger longranger]
|0.2-IGB-gcc-4.9.4-Python-2.7.13
+
|2.1.3<br>2.1.6<br>2.2.2
|quickmerge uses a simple concept to improve contiguity of genome assemblies based on long molecule sequences, often with dramatic outcomes. The program uses information from assemblies made with illumina short reads and PacBio long reads to improve contiguities of an assembly generated with PacBio long reads alone. This is counterintuitive because illumina short reads are not typically considered to cover genomic regions which PacBio long reads cannot. Although we have not evaluated this program for assemblies generated with Oxford nanopore sequences, the program should work with ONP-assemblies too.
+
|Long Ranger is a set of analysis pipelines that processes Chromium sequencing output to align reads and call and phase SNPs, indels, and structural variants. There are five main pipelines, each triggered by a longranger command
 
|-
 
|-
|[http://rnaseq-mats.sourceforge.net/ rMATS]
+
|[http://sourceforge.net/projects/libuuid/ LibUUID]
|3.2.5-IGB-gcc-4.9.4-Python-2.7.13
+
|1.0.3-IGB-gcc-4.9.4
|MATS is a computational tool to detect differential alternative splicing events from RNA-Seq data. The statistical model of MATS calculates the P-value and false discovery rate that the difference in the isoform ratio of a gene between two conditions exceeds a given user-defined threshold. From the RNA-Seq data, MATS can automatically detect and analyze alternative splicing events corresponding to all major types of alternative splicing patterns. MATS handles replicate RNA-Seq data from both paired and unpaired study design.
+
|Portable uuid C library
 
|-
 
|-
|[https://github.com/isovic/racon racon]
+
|[http://qiime.org/ QIIME]
|0.5.0-IGB-gcc-4.9.4-Python-2.7.13<br>0.5.0-IGB-gcc-4.9.4-Python-3.6.1
+
|1.9.1
|Racon is intended as a standalone consensus module to correct raw contigs generated by rapid assembly methods which do not include a consensus step, such as Miniasm.The goal of Racon is to generate genomic consensus which is of similar or better quality compared to the output generated by assembly methods which employ both error correction and consensus steps, while providing a speedup of several times compared to those methods.
+
|QIIME is an open-source bioinformatics pipeline for performing microbiome analysis from raw DNA sequencing data.
 
|-
 
|-
|[http://bioinformatics.psb.ugent.be/supplementary_data/erbon/nov2003/ randfold]
+
|efignt
|2.0.1-IGB-gcc-4.9.4
+
|beta<br>beta_private<br>devel<br>devlocal<br>prod<br>prod_private
|Minimum free energy of folding randomization test software
+
|
 
|-
 
|-
|[https://rclone.org/ rclone]
+
|[http://blast.ncbi.nlm.nih.gov/ BLAST]
|1.41
+
|2.2.26-Linux_x86_64
|Rclone is a command line program to sync files and directories to and from different cloud storage
+
|Basic Local Alignment Search Tool, or BLAST, is an algorithm for comparing primary biological sequence information, such as the amino-acid sequences of different proteins or the nucleotides of DNA sequences.
 
|-
 
|-
|[https://www.rosettacommons.org/ rosetta]
+
|[https://github.com/smirarab/sepp SEPP]
|2017.52-IGB-gcc-4.9.4
+
|20180223-IGB-gcc-4.9.4-Python-2.7.13
|The Rosetta software suite includes algorithms for computational modeling and analysis of protein structures.  
+
|SEPP stands for "SATe-enabled Phylogenetic Placement", and addresses the problem of phylogenetic placement of short reads into reference alignments and trees.
 
|-
 
|-
|[http://rpy.sourceforge.net/ rpy]
+
|[http://www.zeromq.org/bindings:python PyZMQ]
|1.0.3-IGB-gcc-4.9.4-Python-2.7.13-R-2.15.3
+
|16.0.2-IGB-gcc-4.9.4-Python-3.6.1
|RPy is a very simple, yet robust, Python interface to the R Programming Language. Itcan manage all kinds of R objects and can execute arbitrary R functionsincluding the graphic functions.
+
|Python bindings for ZeroMQ
 
|-
 
|-
|[http://rpy.sourceforge.net/ rpy2]
+
|[https://github.com/bbuchfink/diamond DIAMOND]
|2.8.6-IGB-gcc-4.9.4-Python-2.7.13-R-3.3.3<br>2.9.0-IGB-gcc-4.9.4-Python-3.6.1-R-3.3.3
+
|0.8.38-IGB-gcc-4.9.4<br>0.9.10-IGB-gcc-4.9.4<br>0.9.16-IGB-gcc-4.9.4<br>0.9.9-IGB-gcc-4.9.4
|rpy2 is a redesign and rewrite of rpy. It is providing a low-level interface to R from Python, a proposed high-level interface, including wrappers to graphical libraries, as well as R-like structures and functions.
+
|Accelerated BLAST compatible local sequence aligner
 
|-
 
|-
|[https://www.realtimegenomics.com/products/rtg-tools rtg-tools]
+
|[http://www.doxygen.org Doxygen]
|3.8.4
+
|.1.8.13-IGB-gcc-4.9.4<br>1.8.13-IGB-gcc-4.9.4
|RTG Tools contains utilities to easily manipulate and accurately compare multiple VCF files, as well as utilities for processing other common NGS data formats.
+
|Doxygen is a documentation system for C++, C, Java, Objective-C, Python,  IDL (Corba and Microsoft flavors), Fortran, VHDL, PHP, C#, and to some extent D. - Homepage: http://www.doxygen.org
 
|-
 
|-
|[https://github.com/najoshi/sabre sabre]
+
|[http://assemblytics.com/ Assemblytics]
|20171114-IGB-gcc-4.9.4
+
|3f570cd-IGB-gcc-4.9.4<br>df5361f-IGB-gcc-4.9.4
|Next-generation sequencing can currently produce hundreds of millions of reads per lane of sample and that number increases at a dizzying rate. Barcoding individual sequences for multiple lines or multiple species is a cost-efficient method to sequence and analyze a broad range of data.
+
|Analyze your assembly by comparing it to a reference genome
 +
|-
 +
|[https://github.com/rrwick/Porechop Porechop]
 +
|0.2.3-IGB-gcc-4.9.4-Python-3.6.1
 +
|Porechop is a tool for finding and removing adapters from Oxford Nanopore reads.
 +
|-
 +
|[http://dna.ku.dk/%7Esapfo/bammds.html bammds]
 +
|20140602-IGB-gcc-4.9.4
 +
|Software that allows to create a multidimensional scaling (MDS) plot of populations for genetic data.
 +
|-
 +
|[http://www.sqlite.org/ SQLite]
 +
|3.17.0-IGB-gcc-4.9.4
 +
|SQLite: SQL Database Engine in a C Library
 
|-
 
|-
 
|[http://lomereiter.github.io/sambamba/ sambamba]
 
|[http://lomereiter.github.io/sambamba/ sambamba]
Line 1,737: Line 1,741:
 
|sambamba view allows to efficiently filter SAM/BAM/CRAM files for alignments satisfying various conditions, as well as access its SAM header and information about reference sequences.
 
|sambamba view allows to efficiently filter SAM/BAM/CRAM files for alignments satisfying various conditions, as well as access its SAM header and information about reference sequences.
 
|-
 
|-
|[https://github.com/GregoryFaust/samblaster samblaster]
+
|[http://www.freedesktop.org/wiki/Software/HarfBuzz HarfBuzz]
|0.1.24-IGB-gcc-4.9.4
+
|.1.4.6-IGB-gcc-4.9.4
|ummary samblaster is a fast and flexible program for marking duplicates in read-id grouped1 paired-end SAM files. It can also optionally output discordant read pairs and/or split read mappings to separate SAM files, and/or unmapped/clipped reads to a separate FASTQ file. When marking duplicates, samblaster will require approximately 20MB of memory per 1M read pairs.
+
|HarfBuzz is an OpenType text shaping engine. - Homepage: http://www.freedesktop.org/wiki/Software/HarfBuzz
 
|-
 
|-
|[https://github.com/lebedov/scikit-cuda scikit-cuda]
+
|[http://trinityrnaseq.github.io/ Trinity]
|0.5.1-IGB-gcc-4.9.4-Python-2.7.13
+
|2.4.0-IGB-gcc-4.9.4<br>2.5.0-IGB-gcc-4.9.4<br>2.6.5-IGB-gcc-4.9.4
|scikit-cuda provides Python interfaces to many of the functions in the CUDA device/runtime, CUBLAS, CUFFT, and CUSOLVER libraries distributed as part of NVIDIAs CUDA Programming Toolkit, as well as interfaces to select functions in the free and standard versions of the CULA Dense Toolkit. Both low-level wrapper functions similar to their C counterparts and high-level functions comparable to those in NumPy and Scipy are provided.
+
|Trinity represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-Seq data. Trinity combines three independent software modules: Inchworm, Chrysalis, and Butterfly, applied sequentially to process large volumes of RNA-Seq reads. - Homepage: http://trinityrnaseq.github.io/
 
|-
 
|-
|[https://github.com/nanoporetech/scrappie scrappie]
+
|[http://www.libpng.org/pub/png/libpng.html libpng]
|1.3.0-IGB-gcc-4.9.4
+
|.1.6.29-IGB-gcc-4.9.4
|Scrappie is a technology demonstrator for the Oxford Nanopore Research Algorithms group.
+
|libpng is the official PNG reference library - Homepage: http://www.libpng.org/pub/png/libpng.html
 
|-
 
|-
|[https://www.seqan.de/ seqan]
+
|[http://perfsuite.ncsa.illinois.edu/ perfsuite]
|2.3.2-IGB-gcc-4.9.4
+
|1.1.4-IGB-gcc-4.9.4
|SeqAn is an open source C++ library of efficient algorithms and data structures for the analysis of sequences with the focus on biological data
+
|PerfSuite is a collection of tools, utilities, and libraries for software performance analysis where the primary design goals are ease of use, comprehensibility, interoperability, and simplicity. This software can provide a good "entry point" for more detailed performance analysis and can help point the way towards selecting other tools and/or techniques using more specialized software if necessary (for example, tools/libraries from academic research groups or third-party commercial software).
 
|-
 
|-
|[https://github.com/lh3/seqtk/ seqtk]
+
|[http://ghostscript.com GhostScript]
|1.2-IGB-gcc-4.9.4
+
|9.21-IGB-gcc-4.9.4
|Seqtk is a fast and lightweight tool for processing sequences in the FASTA or FASTQ format. It seamlessly parses both FASTA and FASTQ files which can also be optionally compressed by gzip. - Homepage: https://github.com/lh3/seqtk/
+
|Ghostscript is a versatile processor for PostScript data with the ability to render PostScript to different targets. It used to be part of the cups printing stack, but is no longer used for that. - Homepage: http://ghostscript.com
 
|-
 
|-
|[https://mathgen.stats.ox.ac.uk/genetics_software/shapeit/shapeit.html shapeit]
+
|[http://cnswww.cns.cwru.edu/php/chet/readline/rltop.html libreadline]
|2.20
+
|.6.3-IGB-gcc-4.9.4
|SHAPEIT is a fast and accurate method for estimation of haplotypes (aka phasing) from genotype or sequencing data.
+
|The GNU Readline library provides a set of functions for use by applications that allow users to edit command lines as they are typed in. Both Emacs and vi editing modes are available. The Readline library includes additional functions to maintain a list of previously-entered command lines, to recall and perhaps reedit those lines, and perform csh-like history expansion on previous commands. - Homepage: http://cnswww.cns.cwru.edu/php/chet/readline/rltop.html
 
|-
 
|-
|[https://www.gnu.org/software/sharutils/ sharutils]
+
|[http://www.circos.ca/ Circos]
|4.15.2-IGB-gcc-4.9.4
+
|0.69-4-IGB-gcc-4.9.4-Perl-5.24.1
|GNU shar makes so-called shell archives out of many files, preparing them for transmission by electronic mail services, while unshar helps unpacking shell archives after reception.
+
|Circos is a software package for visualizing data and information. It visualizes data in a circular layout - this makes Circos ideal for exploring relationships between objects or positions. - Homepage: http://www.circos.ca/
 
|-
 
|-
|[http://lowelab.ucsc.edu/snoscan/ snoscan]
+
|[http://www.gnu.org/software/gsl/ GSL]
|0.9.1-IGB-gcc-4.9.4-Perl-5.24.1<br>0.9.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
+
|2.3-IGB-gcc-4.9.4
|Search for C/D box methylation guide snoRNA genes in a genomic sequence
+
|The GNU Scientific Library (GSL) is a numerical library for C and C++ programmers. The library provides a wide range of mathematical routines such as random number generators, special functions and least-squares fitting. - Homepage: http://www.gnu.org/software/gsl/
 
|-
 
|-
|[http://sourceforge.net/projects/snpeff/ snpEff]
+
|[http://www.unidata.ucar.edu/software/udunits/ udunits]
|4.3o-Java-1.8.0_121
+
|2.2.26-IGB-gcc-4.9.4
|SnpEff is a variant annotation and effect prediction tool.  It annotates and predicts the effects of genetic variants (such as amino acid changes).
+
|UDUNITS supports conversion of unit specifications between formatted and binary forms, arithmetic manipulation of units, and conversion of values between compatible scales of measurement.
 
|-
 
|-
|[https://github.com/magnusmanske/snpomatic snpomatic]
+
|[http://pillow.readthedocs.org/ Pillow]
|1.0-IGB-gcc-4.9.4
+
|5.1.0-IGB-gcc-4.9.4-Python-2.7.13<br>5.1.0-IGB-gcc-4.9.4-Python-3.6.1
|SNP-o-matic is a fast, stringent short-read mapping software. It supports a multitude of output types and formats, for uses in filtering reads, alignments, sequence-based genotyping calls, assisted reassembly of contigs etc.
+
|Pillow is the friendly PIL fork by Alex Clark and Contributors. PIL is the Python Imaging Library by Fredrik Lundh and Contributors.
 
|-
 
|-
|[https://github.com/sparsehash/sparsehash sparsehash]
+
|[http://www.tcl.tk/ Tcl]
|2.0.3-IGB-gcc-4.9.4
+
|8.6.6-IGB-gcc-4.9.4
|This directory contains several hash-map implementations, similar inAPI to SGIs hash_map class, but with different performance characteristics.
+
|Tcl (Tool Command Language) is a very powerful but easy to learn dynamic programming language,suitable for a very wide range of uses, including web and desktop applications, networking, administration,testing and many more. - Homepage: http://www.tcl.tk/
 
|-
 
|-
|[http://eddylab.org/software.html squid]
+
|[http://www.repeatmasker.org/ RepeatMasker]
|1.9g-IGB-gcc-4.9.4
+
|4.0.7-IGB-gcc-4.9.4-Perl-5.24.1<br>4.0.7-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
|A C library that is bundled with much of the above software. C function library for sequence analysis.
+
|RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences.  
 
|-
 
|-
|[http://www.sanger.ac.uk/science/tools/ssaha2-0 ssaha2]
+
|[http://ipython.org/index.html IPython]
|2.5.5-IGB-gcc-4.9.4
+
|5.3.0-IGB-gcc-4.9.4-Python-3.6.1
|SSAHA2 (Sequence Search and Alignment by Hashing Algorithm) is a pairwise sequence alignment program designed for the efficient mapping of sequencing reads onto genomic reference sequences.
+
|IPython provides a rich architecture for interactive computing with: Powerful interactive shells (terminal and Qt-based). A browser-based notebook with support for code, text, mathematical expressions, inline plots and other rich media. Support for interactive data visualization and use of GUI toolkits. Flexible, embeddable interpreters to load into your own projects. Easy to use, high performance tools for parallel computing.
 
|-
 
|-
|[http://www.sanger.ac.uk/science/tools/ssaha2-0 ssaha_pileup]
+
|[http://xcb.freedesktop.org/ libpthread-stubs]
|0.6-IGB-gcc-4.9.4
+
|.0.3-IGB-gcc-4.9.4
|SSAHA2: Sequence Search and Alignment by Hashing Algorithm
+
|The X protocol C-language Binding (XCB) is a replacement for Xlib featuring a small footprint,latency hiding, direct access to the protocol, improved threading support, and extensibility.
 
|-
 
|-
|[https://web.stanford.edu/group/pritchardlab/structure.html structure]
+
|[https://github.com/laurikari/tre tre]
|2.3.4-IGB-gcc-4.9.4
+
|20161208-IGB-gcc-4.9.4
|The program structure is a free software package for using multi-locus genotype data to investigate population structure.
+
|TRE is a lightweight, robust, and efficient POSIX compliant regexp matching library with some exciting features such as approximate (fuzzy) matching.The matching algorithm used in TRE uses linear worst-case time in the length of the text being searched, and quadratic worst-case time in the length of the used regular expression.In other words, the time complexity of the algorithm is O(M^2N), where M is the length of the regular expression and N is the length of the text. The used space is also quadratic on the length of the regex, but does not depend on the searched string. This quadratic behaviour occurs only on pathological cases which are probably very rare in practice.
 
|-
 
|-
|[http://swift-lang.org/Swift-T/ swift-t]
+
|[https://github.com/google/googletest gtest]
|1.3-IGB-gcc-4.9.4
+
|1.8.0-IGB-gcc-4.9.4
|Swift/T is a completely new implementation of the Swift language for high-performance computing. In this implementation, the Swift script is translated into an MPI program that uses the Turbine (hence, /T) and ADLB runtime libraries for highly scalable dataflow processing over MPI, without single-node bottlenecks.
+
|Googles C++ test framework
 
|-
 
|-
|[http://lowelab.ucsc.edu/tRNAscan-SE/ tRNAscan-SE]
+
|[http://research-pub.gene.com/gmap/ GMAP-GSNAP]
|1.3.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
+
|2017-11-15-IGB-gcc-4.9.4
|tRNAscan-SE: a tool for finding transfer RNAs
+
|GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences GSNAP: Genomic Short-read Nucleotide Alignment Program
 
|-
 
|-
|[http://samtools.sourceforge.net tabix]
+
|[http://mummer.sourceforge.net/ MUMmer]
|0.2.6-IGB-gcc-4.9.4
+
|3.23-IGB-gcc-4.9.4<br>4.0.0beta2-IGB-gcc-4.9.4
|Generic indexer for TAB-delimited genome position files
+
|MUMmer is a system for rapidly aligning entire genomes, whether in complete or draft form. AMOS makes use of it.
 
|-
 
|-
|[https://github.com/lvclark/tagdigger tagdigger]
+
|[http://broadinstitute.github.io/picard/ picard]
|1.1-IGB-gcc-4.9.4-Python-3.6.1
+
|2.10.1-Java-1.8.0_121<br>2.10.1-Java-1.8.0_152<br>2.9.0-Java-1.8.0_121<br>2.9.4-Java-1.8.0_121
|TagDigger is a program for processing FASTQ files from genotyping-by-sequencing (GBS) or restriction site-associated DNA sequencing (RAD-seq) experiments.  
+
|A set of tools (in Java) for working with next generation sequencing data in the BAM  (http://samtools.github.io/hts-specs) format.
 
|-
 
|-
|[http://software.intel.com/en-us/articles/intel-tbb/ tbb]
+
|[http://www.gdal.org/ GDAL]
|.2017_U5-IGB-gcc-4.9.4
+
|2.3.1-IGB-gcc-4.9.4
|Intel Threading Building Blocks 4.0 (Intel TBB) is a widely used, award-winning C++ template library for creating reliable, portable, and scalable parallel applications. Use Intel TBB for a simple and rapid way of developing robust task-based parallel applications that scale to available processor cores, are compatible with multiple environments, and are easier to maintain. Intel TBB is the most proficient way to implement future-proof parallel applications that tap into the power and performance of multicore and manycore hardware platforms. - Homepage: http://software.intel.com/en-us/articles/intel-tbb/
+
|GDAL is a translator library for raster geospatial data formats that is released under an X/MIT style Open Source license by the Open Source Geospatial Foundation. As a library, it presents a single abstract data model to the calling application for all supported formats. It also comes with a variety of useful commandline utilities for data translation and processing.
 
|-
 
|-
|[https://www.ncbi.nlm.nih.gov/genbank/tbl2asn2/ tbl2asn]
+
|[http://swift-lang.org/Swift-T/ swift-t]
|20180516
+
|1.3-IGB-gcc-4.9.4
|Tbl2asn is a command-line program that automates the creation of sequence records for submission to GenBank
+
|Swift/T is a completely new implementation of the Swift language for high-performance computing. In this implementation, the Swift script is translated into an MPI program that uses the Turbine (hence, /T) and ADLB runtime libraries for highly scalable dataflow processing over MPI, without single-node bottlenecks.
 
|-
 
|-
|[http://tensorly.org/stable/home.html tensorly]
+
|[https://www.ffmpeg.org/ FFmpeg]
|0.4.2-IGB-gcc-4.9.4-Python-3.6.1
+
|3.3-IGB-gcc-4.9.4
|Simple and Fast Tensor Learning in Python
+
|A complete, cross-platform solution to record, convert and stream audio and video. - Homepage: https://www.ffmpeg.org/
 
|-
 
|-
|[https://www.tug.org/texlive/ texlive]
+
|[https://www.ebi.ac.uk/about/vertebrate-genomics/software/exonerate exonerate]
|20170520-IGB-gcc-4.9.4
+
|2.2.0-IGB-gcc-4.9.4
|TeX Live is an easy way to get up and running with the TeX document production system. It provides a comprehensive TeX system with binaries for most flavors of Unix, including GNU/Linux, and also Windows. It includes all the major TeX-related programs, macro packages, and fonts that are free software, including support for many languages around the world.  
+
|Exonerate is a generic tool for pairwise sequence comparison. It allows you to align sequences using a many alignment models, either exhaustive dynamic programming or a variety of heuristics.
 
|-
 
|-
|[http://hibberdlab.com/transrate/ transrate]
+
|[https://trinotate.github.io/ Trinotate]
|1.0.3
+
|3.1.1-IGB-gcc-4.9.4-Perl-5.24.1
|Transrate is software for de-novo transcriptome assembly quality analysis. It examines your assembly in detail and compares it to experimental evidence such as the sequencing reads, reporting quality scores for contigs and assemblies.
+
|Trinotate is a comprehensive annotation suite designed for automatic functional annotation of transcriptomes, particularly de novo assembled transcriptomes, from model or non-model organisms. Trinotate makes use of a number of different well referenced methods for functional annotation including homology search to known sequence data (BLAST+/SwissProt), protein domain identification (HMMER/PFAM), protein signal peptide and transmembrane domain prediction (signalP/tmHMM), and leveraging various annotation databases (eggNOG/GO/Kegg databases). All functional annotation data derived from the analysis of transcripts is integrated into a SQLite database which allows fast efficient searching for terms with specific qualities related to a desired scientific hypothesis or a means to create a whole annotation report for a transcriptome.
 
|-
 
|-
|[https://github.com/laurikari/tre tre]
+
|[http://clusterflow.io/ clusterflow]
|20161208-IGB-gcc-4.9.4
+
|0.5-IGB-gcc-4.9.4-Perl-5.25.1
|TRE is a lightweight, robust, and efficient POSIX compliant regexp matching library with some exciting features such as approximate (fuzzy) matching.The matching algorithm used in TRE uses linear worst-case time in the length of the text being searched, and quadratic worst-case time in the length of the used regular expression.In other words, the time complexity of the algorithm is O(M^2N), where M is the length of the regular expression and N is the length of the text. The used space is also quadratic on the length of the regex, but does not depend on the searched string. This quadratic behaviour occurs only on pathological cases which are probably very rare in practice.
+
|Cluster Flow is workflow manager designed to run bioinformatics pipelines. It is operated through a single command cf, which can be used to launch, configure, monitor and cancel pipelines.
 
|-
 
|-
|[https://bitbucket.org/nygcresearch/treemix treemix]
+
|[https://github.com/uoregon-postlethwait/prost Prost]
|1.13-IGB-gcc-4.9.4
+
|0.7.45-IGB-gcc-4.9.4-Python-2.7.13
|TreeMix is a method for inferring the patterns of population splits and mixtures in the history of a set of populations. In the underlying model, the modern-day populations in a species are related to a common ancestor via a graph of ancestral populations. We use the allele frequencies in the modern populations to infer the structure of this graph.
+
|Prost (PRocessing Of Small Transcripts) is a python application that quantifies and annotates microRNA (miRNA) expression in metazoans with assembled genomes. Prost works by counting short transcripts within a user-specifiable length range. These counted transcripts are aligned to a user specifiable genome allowing for post-transcriptional modification (e.g. untemplated additions, editing, alternative cutting) and then "binned" together based on genomic location. Each bin is then annotated with databases of mature miRNAs, hairpins, and other types of RNAs (the databases may be derived from miRBase, Ensembls BioMart, other databases, or may be custom built by the user).
 
|-
 
|-
|[http://tandem.bu.edu/trf/trf.html trf]
+
|[http://micans.org/mcl/ MCL]
|4.0.9
+
|14.137-IGB-gcc-4.9.4
|Tandem Repeats Finder is a program to locate and display tandem repeats in DNA sequences.  
+
|The MCL algorithm is short for the Markov Cluster Algorithm, a fastand scalable unsupervised cluster algorithm for graphs (also known as networks) basedon simulation of (stochastic) flow in graphs. - Homepage: http://micans.org/mcl/
 
|-
 
|-
|[http://www.unidata.ucar.edu/software/udunits/ udunits]
+
|[http://www.boost.org/ Boost]
|2.2.26-IGB-gcc-4.9.4
+
|.1.59.0-IGB-gcc-4.9.4<br>.1.63.0-IGB-gcc-4.9.4<br>.1.63.0-IGB-gcc-4.9.4-Python-2.7.13
|UDUNITS supports conversion of unit specifications between formatted and binary forms, arithmetic manipulation of units, and conversion of values between compatible scales of measurement.
+
|Boost provides free peer-reviewed portable C++ source libraries. - Homepage: http://www.boost.org/
 
|-
 
|-
|[https://github.com/PacificBiosciences/unanimity/ unanimity]
+
|[https://github.com/broadinstitute/pilon pilon]
|20180307-IGB-gcc-4.9.4
+
|1.22-Java-1.8.0_121
|C++ library and its applications to generate and process accurate consensus sequences
+
|Pilon is a software tool which can be used to:- Automatically improve draft assemblies- Find variation among strains, including large event detection
 
|-
 
|-
|[http://valgrind.org/downloads/ valgrind]
+
|[https://github.com/arq5x/poretools h5py]
|3.13.0-IGB-gcc-4.9.4
+
|.2.7.0-IGB-gcc-4.9.4-Python-2.7.13<br>2.7.0-IGB-gcc-4.9.4-Python-2.7.13
|Valgrind is an instrumentation framework for building dynamic analysis tools. There are Valgrind tools that can automatically detect many memory management and threading bugs, and profile your programs in detail. You can also use Valgrind to build new tools.
+
|a toolkit for working with nanopore sequencing data from Oxford Nanopore. - Homepage: https://github.com/arq5x/poretools
 
|-
 
|-
|[https://www.ebi.ac.uk/~zerbino/velvet/ velvet]
+
|[https://bedops.readthedocs.io/en/latest/ bedops]
|1.2.10-IGB-gcc-4.9.4-kmer_121
+
|2.4.30
|Velvet is a de novo genomic assembler specially designed for short read sequencing technologies, such as Solexa or 454, developed by Daniel Zerbino and Ewan Birney at the European Bioinformatics Institute (EMBL-EBI), near Cambridge, in the United Kingdom.  
+
|BEDOPS is an open-source command-line toolkit that performs highly efficient and scalable Boolean and other set operations, statistical calculations, archiving, conversion and other management of genomic data of arbitrary scale.  
 
|-
 
|-
|[http://www.videolan.org/developers/x264.html x264]
+
|[http://invisible-island.net/byacc/byacc.html byacc]
|.20170604-IGB-gcc-4.9.4
+
|20170709-IGB-gcc-4.9.4
|x264 is a free software library and application for encoding video streams into the H.264/MPEG-4 AVC compression format, and is released under the terms of the GNU GPL. - Homepage: http://www.videolan.org/developers/x264.html
+
|Berkeley Yacc (byacc) is generally conceded to be the best yacc variant available.In contrast to bison, it is written to avoid dependencies upon a particular compiler.
 
|-
 
|-
|[https://github.com/dmlc/xgboost xgboost]
+
|[http://www.repeatmasker.org/RMBlast.html RMBlast]
|0.80-IGB-gcc-4.9.4-Python-3.6.1
+
|2.6.0-IGB-gcc-4.9.4
|XGBoost is an optimized distributed gradient boosting library designed to be highly efficient, flexible and portable. It implements machine learning algorithms under the Gradient Boosting framework.
+
|RMBlast is a RepeatMasker compatible version of the standard NCBI blastn program. The primary difference between this distribution and the NCBI distribution is the addition of a new program "rmblastn" for use with RepeatMasker and RepeatModeler.
 
|-
 
|-
|[http://cgit.freedesktop.org/xorg/util/macros xorg-macros]
+
|efiest
|.1.19.0-IGB-gcc-4.9.4
+
|beta<br>beta_private<br>devel<br>devlocal<br>prod<br>prod_private
|X.org macros utilities.
+
|
|-
 
|[http://www.zlib.net/ zlib]
 
|.1.2.11<br>.1.2.11-GCCcore-4.9.4<br>.1.2.11-IGB-gcc-4.9.4
 
|zlib is designed to be a free, general-purpose, legally unencumbered -- that is, not covered by any patents -- lossless data-compression library for use on virtually any computer hardware and operating system. - Homepage: http://www.zlib.net/
 
 
|}
 
|}

Revision as of 14:36, 14 September 2018

Application Installed Versions Description
PePr 1.1.21-IGB-gcc-4.9.4-Python-2.7.13 PePr is a ChIP-Seq Peak-calling and Prioritization pipeline that uses a sliding window approach and models read counts across replicates and between groups with a negative binomial distribution.
SDL2 2.0.4-IGB-gcc-4.9.4 SDL: Simple DirectMedia Layer, a cross-platform multimedia library
scikit-cuda 0.5.1-IGB-gcc-4.9.4-Python-2.7.13 scikit-cuda provides Python interfaces to many of the functions in the CUDA device/runtime, CUBLAS, CUFFT, and CUSOLVER libraries distributed as part of NVIDIAs CUDA Programming Toolkit, as well as interfaces to select functions in the free and standard versions of the CULA Dense Toolkit. Both low-level wrapper functions similar to their C counterparts and high-level functions comparable to those in NumPy and Scipy are provided.
NASM .2.12.02-IGB-gcc-4.9.4
2.12.02-IGB-gcc-4.9.4
NASM: General-purpose x86 assembler
Perl 5.24.1-IGB-gcc-4.9.4
5.24.1-IGB-gcc-4.9.4-bare
5.26.1-IGB-gcc-4.9.4-unthreaded
Larry Wall Practical Extraction and Report Language
mapDamage 2.0.5-IGB-gcc-4.9.4-Python-2.7.13 mapDamage2 is a computational framework written in Python and R, which tracks and quantifies DNA damage patterns among ancient DNA sequencing reads generated by Next-Generation Sequencing platforms.
libjpeg-turbo .1.5.1-IGB-gcc-4.9.4 libjpeg-turbo is a fork of the original IJG libjpeg which uses SIMD to accelerate baseline JPEGcompression and decompression. libjpeg is a library that implements JPEG image encoding, decoding and transcoding. - Homepage: http://sourceforge.net/projects/libjpeg-turbo/
VSEARCH 2.4.3-IGB-gcc-4.9.4 VSEARCH stands for vectorized search, as the tool takes advantage of parallelism in the form of SIMD vectorization as well as multiple threads to perform accurate alignments at high speed. - Homepage: https://github.com/torognes/vsearch
transrate 1.0.3 Transrate is software for de-novo transcriptome assembly quality analysis. It examines your assembly in detail and compares it to experimental evidence such as the sequencing reads, reporting quality scores for contigs and assemblies.
MACS2 2.1.1.20160309-IGB-gcc-4.9.4-Python-2.7.13 Model Based Analysis for ChIP-Seq data - Homepage: https://github.com/taoliu/MACS/
Subread 1.5.2-IGB-gcc-4.9.4 High performance read alignment, quantification and mutation discovery - Homepage: http://subread.sourceforge.net/
igv 2.4.4-Java-1.8.0_152 The Integrative Genomics Viewer (IGV) is a high-performance visualization tool for interactive exploration of large, integrated genomic datasets. It supports a wide variety of data types, including array-based and next-generation sequence data, and genomic annotations.
RNAhybrid 2.1.2-IGB-gcc-4.9.4 RNAhybrid is a tool for finding the minimum free energy hybridization of a long and a short RNA. The hybridization is performed in a kind of domain mode, ie. the short sequence is hybridized to the best fitting part of the long one. The tool is primarily meant as a means for microRNA target prediction.
SignalP 4.1 Signal peptide and cleavage sites in gram+, gram- and eukaryotic amino acid sequences
GraphicsMagick 1.3.26-IGB-gcc-4.9.4 GraphicsMagick is the swiss army knife of image processing.
libdrm .2.4.76-IGB-gcc-4.9.4 Direct Rendering Manager runtime library.
SNAP 2013-11-29-IGB-gcc-4.9.4 (Semi-HMM-based Nucleic Acid Parser) gene prediction tool
novocraft 3.08.00 Powerful tool designed for mapping of short reads onto a reference genome from Illumina, Ion Torrent, and 454 NGS platforms.
GMAP 2018-05-30-IGB-gcc-4.9.4 A Genomic Mapping and Alignment Program for mRNA and EST Sequences, andGSNAP: Genomic Short-read Nucleotide Alignment Program
MToolBox 1.0-IGB-gcc-4.9.4 MToolBox is a highly automated bioinformatics pipeline to reconstruct and analyze human mitochondrial DNA from high throughput sequencing data. MToolBox includes an updated computational strategy to assemble mitochondrial genomes from Whole Exome and/or Genome Sequencing (PMID: 22669646) and an improved fragment-classify tool (PMID:22139932) for haplogroup assignment, functional and prioritization analysis of mitochondrial variants. MToolBox provides pathogenicity scores, profiles of genome variability and disease-associations for mitochondrial variants. MToolBox provides also a Variant Call Format file (version 4.0) featuring, for the first time, allele-specific heteroplasmy.
a2ps 4.14-IGB-gcc-4.9.4 a2ps-4.14: Formats an ascii file for printing on a postscript printer
PAGAN 20150723-IGB-gcc-4.9.4 PAGAN is a general-purpose method for the alignment of sequence graphs. PAGAN is based on the phylogeny-aware progressive alignment algorithm and uses graphs to describe the uncertainty in the presence of characters at certain sequence positions. However, graphs also allow describing the uncertainty in input sequences and modelling e.g. homopolymer errors in Roche 454 reads, or representing inferred ancestral sequences against which other sequences can then be aligned. PAGAN is still under development and will hopefully evolve to an easy-to-use, general-purpose method for phylogenetic sequence alignment.
deepTools 2.5.3-IGB-gcc-4.9.4-Python-2.7.13
3.0.1-IGB-gcc-4.9.4-Python-2.7.13
deepTools addresses the challenge of handling the large amounts of data that are now routinely generated from DNA sequencing centers. deepTools contains useful modules to process the mapped reads data for multiple quality checks, creating normalized coverage files in standard bedGraph and bigWig file formats, that allow comparison between different files (for example, treatment and control). Finally, using such normalized and standardized files, deepTools can create many publication-ready visualizations to identify enrichments and for functional annotations of the genome.
rMATS 3.2.5-IGB-gcc-4.9.4-Python-2.7.13 MATS is a computational tool to detect differential alternative splicing events from RNA-Seq data. The statistical model of MATS calculates the P-value and false discovery rate that the difference in the isoform ratio of a gene between two conditions exceeds a given user-defined threshold. From the RNA-Seq data, MATS can automatically detect and analyze alternative splicing events corresponding to all major types of alternative splicing patterns. MATS handles replicate RNA-Seq data from both paired and unpaired study design.
GFOLD 1.1.4-IGB-gcc-4.9.4 GFOLD stands for Generalized FOLD change for ranking differentially expressed genes from RNA-seq data. GFOLD is especially useful when no replicate is available. GFOLD generalizes the fold change by considering the posterior distribution of log fold change, such that each gene is assigned a reliable fold change.
M4 .1.4.17-IGB-gcc-4.9.4
.1.4.18
.1.4.18-GCCcore-4.9.4
.1.4.18-IGB-gcc-4.9.4
GNU M4 is an implementation of the traditional Unix macro processor. It is mostly SVR4 compatible although it has some extensions (for example, handling more than 9 positional parameters to macros). GNU M4 also has built-in functions for including files, running shell commands, doing arithmetic, etc.
Falcon2Fastg 0.3.1-IGB-gcc-4.9.4-Python-2.7.13 This software converts the results of PacBio assembly using FALCON, to a FASTG graph that can be visualized using Bandage.
samblaster 0.1.24-IGB-gcc-4.9.4 ummary samblaster is a fast and flexible program for marking duplicates in read-id grouped1 paired-end SAM files. It can also optionally output discordant read pairs and/or split read mappings to separate SAM files, and/or unmapped/clipped reads to a separate FASTQ file. When marking duplicates, samblaster will require approximately 20MB of memory per 1M read pairs.
snoscan 0.9.1-IGB-gcc-4.9.4-Perl-5.24.1
0.9.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
Search for C/D box methylation guide snoRNA genes in a genomic sequence
tagdigger 1.1-IGB-gcc-4.9.4-Python-3.6.1 TagDigger is a program for processing FASTQ files from genotyping-by-sequencing (GBS) or restriction site-associated DNA sequencing (RAD-seq) experiments.
ea-utils 1.04.807-IGB-gcc-4.9.4 Command-line tools for processing biological sequencing data. Barcode demultiplexing, adapter trimming, etc. Primarily written to support an Illumina based pipeline - but should work with any FASTQs.
PEAR 0.9.8-IGB-gcc-4.9.4 PEAR is an ultrafast, memory-efficient and highly accurate pair-end read merger. It is fully parallelized and can run with as low as just a few kilobytes of memory. - Homepage: http://sco.h-its.org/exelixis/web/software/pear/
HMMER 2.3.2-IGB-gcc-4.9.4
3.1b2-IGB-gcc-4.9.4
3.2.1-IGB-gcc-4.9.4
HMMER is used for searching sequence databases for homologs of protein sequences, and for making protein sequence alignments. It implements methods using probabilistic models called profile hidden Markov models (profile HMMs). Compared to BLAST, FASTA, and other sequence alignment and database search tools based on older scoring methodology, HMMER aims to be significantly more accurate and more able to detect remote homologs because of the strength of its underlying mathematical models. In the past, this strength came at significant computational expense, but in the new HMMER3 project, HMMER is now essentially as fast as BLAST.
rpy2 2.8.6-IGB-gcc-4.9.4-Python-2.7.13-R-3.3.3
2.9.0-IGB-gcc-4.9.4-Python-3.6.1-R-3.3.3
rpy2 is a redesign and rewrite of rpy. It is providing a low-level interface to R from Python, a proposed high-level interface, including wrappers to graphical libraries, as well as R-like structures and functions.
pkg-config .0.29.2-IGB-gcc-4.9.4 pkg-config is a helper tool used when compiling applications and libraries. It helps you insert the correct compiler options on the command line so an application can use gcc -o test test.c `pkg-config --libs --cflags glib-2.0` for instance, rather than hard-coding values on where to find glib (or other libraries). - Homepage: http://www.freedesktop.org/wiki/Software/pkg-config/
Trimmomatic 0.36-Java-1.8.0_121
0.36-Java-1.8.0_152
0.38-Java-1.8.0_152
Trimmomatic performs a variety of useful trimming tasks for illumina paired-end and single ended data.The selection of trimming steps and their associated parameters are supplied on the command line.
LAME 3.99.5-IGB-gcc-4.9.4 LAME is a high quality MPEG Audio Layer III (MP3) encoder licensed under the LGPL.
flex .2.6.3
.2.6.3-GCCcore-4.9.4
Flex (Fast Lexical Analyzer) is a tool for generating scanners. A scanner, sometimes called a tokenizer, is a program which recognizes lexical patterns in text. - Homepage: http://flex.sourceforge.net/
InterProScan 5.27-66.0-IGB-gcc-4.9.4-Java-1.8.0_152
5.28-67.0-IGB-gcc-4.9.4-Java-1.8.0_152
InterProScan is the software package that allows sequences (protein and nucleic) to be scanned against InterPros signatures. Signatures are predictive models, provided by several different databases, that make up the InterPro consortium.
pygpu 0.6.5-IGB-gcc-4.9.4-Python-2.7.13 Python bindings for libgpuarray - Homepage: http://deeplearning.net/software/libgpuarray
Qt 4.8.7-IGB-gcc-4.9.4 Qt is a comprehensive cross-platform C++ application framework.
Gradle 4.7 Complete Gradle install.From mobile apps to microservices, from small startups to big enterprises,Gradle helps teams build, automate and deliver better software, faster.
PyTorch 0.3.0-IGB-gcc-4.9.4-Python-3.6.1
0.4.0-IGB-gcc-4.9.4-Python-3.6.1
Tensors and Dynamic neural networks in Pythonwith strong GPU acceleration.
libgtextutils .0.7-IGB-gcc-4.9.4 ligtextutils is a dependency of fastx-toolkit and is provided via the same upstream - Homepage: http://hannonlab.cshl.edu/fastx_toolkit/
MEGAHIT 1.1.1-IGB-gcc-4.9.4 MEGAHIT is a single node assembler for large and complex metagenomics NGS reads, such as soil. It makes use of succinct de Bruijn graph (SdBG) to achieve low memory assembly. - Homepage: https://github.com/voutcn/megahit
git 2.9.5-IGB-gcc-4.9.4 Git is a free and open source distributed version control system designedto handle everything from small to very large projects with speed and efficiency.
Biopieces 2.0-IGB-gcc-4.9.4-Perl-5.24.1 Biopieces is a bioinformatic framework of tools easily used and easily created.
VCFtools 0.1.15-IGB-gcc-4.9.4-Perl-5.24.1 The aim of VCFtools is to provide easily accessible methods for working with complex genetic variation data in the form of VCF files. - Homepage: https://vcftools.github.io
CUDA 8.0.61-IGB-gcc-4.9.4
9.0.176-IGB-gcc-4.9.4
9.1.85-IGB-gcc-4.9.4
CUDA (formerly Compute Unified Device Architecture) is a parallel computing platform and programming model created by NVIDIA and implemented by the graphics processing units (GPUs) that they produce. CUDA gives developers access to the virtual instruction set and memory of the parallel computational elements in CUDA GPUs. - Homepage: https://developer.nvidia.com/cuda-toolkit
MEME 4.12.0-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
5.0.1-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
The MEME Suite allows you to: * discover motifs using MEME, DREME (DNA only) or GLAM2 on groups of related DNA or protein sequences, * search sequence databases with motifs using MAST, FIMO, MCAST or GLAM2SCAN, * compare a motif to all motifs in a database of motifs, * associate motifs with Gene Ontology terms via their putative target genes, and * analyse motif enrichment using SpaMo or CentriMo.
IllinoisDataBank 1.0-IGB-gcc-4.9.4-Python-2.7.13 The Illinois Data Bank is a public access repository for publishing research data from the University of Illinois at Urbana-Champaign - Homepage: https://databank.illinois.edu/
kentUtils 353-IGB-gcc-4.9.4 UCSC genome browser kent bioinformatic utilities
QIIME2 2017.10
2017.11
2017.12
2017.6
2017.8
2018.2
2018.4
2018.6
QIIME is an open-source bioinformatics pipeline for performing microbiome analysis from raw DNA sequencing data.
argtable .2.13-IGB-gcc-4.9.4 Argtable is an ANSI C library for parsing GNU style command line options with a minimum of fuss. - Homepage: http://argtable.sourceforge.net/
tbb .2017_U5-IGB-gcc-4.9.4 Intel Threading Building Blocks 4.0 (Intel TBB) is a widely used, award-winning C++ template library for creating reliable, portable, and scalable parallel applications. Use Intel TBB for a simple and rapid way of developing robust task-based parallel applications that scale to available processor cores, are compatible with multiple environments, and are easier to maintain. Intel TBB is the most proficient way to implement future-proof parallel applications that tap into the power and performance of multicore and manycore hardware platforms. - Homepage: http://software.intel.com/en-us/articles/intel-tbb/
VirSorter 20170215-IGB-gcc-4.9.4-Perl-5.24.1 VirSorter: mining viral signal from microbial genomic data.
GeneMarkS 4.30-IGB-gcc-4.9.4 GeneMarkS: a self-training method for prediction of gene starts in microbial genomes
gdb 8.0.1-IGB-gcc-4.9.4-Python-2.7.13 The GNU Project Debugger
Pysam 0.13.0-IGB-gcc-4.9.4-Python-2.7.13
0.13.0-IGB-gcc-4.9.4-Python-3.6.1
Pysam is a python module for reading and manipulating Samfiles. Its a lightweight wrapper of the samtools C-API. Pysam also includes an interface for tabix.
sabre 20171114-IGB-gcc-4.9.4 Next-generation sequencing can currently produce hundreds of millions of reads per lane of sample and that number increases at a dizzying rate. Barcoding individual sequences for multiple lines or multiple species is a cost-efficient method to sequence and analyze a broad range of data.
DANPOS 2.2.2-IGB-gcc-4.9.4-Python-2.7.13-R-3.3.3 A toolkit for Dynamic Analysis of Nucleosome and Protein Occupancy by Sequencing, version 2
microbiome_helper 20171114-IGB-gcc-4.9.4 An assortment of scripts to help process and automate various microbiome and metagenomic bioinformatic tools. We provide workflows, tutorials and a virtual box image to help researchers process microbial data.
Infernal 1.1.2-IGB-gcc-4.9.4 Infernal,INFERence of RNA ALignment, is for searching DNA sequence databases for RNA structure and sequence similarities.
MapSplice 2.2.1-IGB-gcc-4.9.4-Python-2.7.13 MapSplice is a software for mapping RNA-seq data to reference genome for splice junction discovery that depends only on reference genome, and not on any further annotations.
OpenCV 3.1.0-IGB-gcc-4.9.4-Python-2.7.13
3.3.0-IGB-gcc-4.9.4-Python-3.6.1
OpenCV (Open Source Computer Vision Library) is an open source computer vision and machine learning software library. OpenCV was built to provide a common infrastructure for computer vision applications and to accelerate the use of machine perception in the commercial products.
ClustalW2 2.1-IGB-gcc-4.9.4 ClustalW2 is a general purpose multiple sequence alignment program for DNA or proteins. - Homepage: http://www.ebi.ac.uk/Tools/msa/clustalw2/
Phantompeaktools 1.2-IGB-gcc-4.9.4-R-3.4.1 Custom SPP for Phantompeaktools
gnuplot 4.6.7-IGB-gcc-4.9.4
5.0.6-IGB-gcc-4.9.4
Portable interactive, function plotting utility - Homepage: http://gnuplot.sourceforge.net/
MultiQC 0.9-IGB-gcc-4.9.4-Python-2.7.13
1.2-IGB-gcc-4.9.4-Python-2.7.13
1.2-IGB-gcc-4.9.4-Python-3.6.1
MultiQC searches a given directory for analysis logs and compiles a HTML report. Its a general use tool, perfect for summarising the output from numerous bioinformatics tools.
ABySS 2.0.2-IGB-gcc-4.9.4 ABySS is a de novo, parallel, paired-end sequence assembler that is designed for short reads. The single-processor version is useful for assembling genomes up to 100 Mbases in size. The parallel version is implemented using MPI and is capable of assembling larger genomes.
hwloc .1.11.6-GCC-4.9.4-2.28 The Portable Hardware Locality (hwloc) software package provides a portable abstraction(across OS, versions, architectures, ...) of the hierarchical topology of modern architectures, includingNUMA memory nodes, sockets, shared caches, cores and simultaneous multithreading. It also gathers varioussystem attributes such as cache and memory information as well as the locality of I/O devices such asnetwork interfaces, InfiniBand HCAs or GPUs. It primarily aims at helping applications with gatheringinformation about modern computing hardware so as to exploit it accordingly and efficiently. - Homepage: http://www.open-mpi.org/projects/hwloc/
protobuf 2.6.1-IGB-gcc-4.9.4
3.5.0-IGB-gcc-4.9.4
Protocol Buffers (a.k.a., protobuf) are Googles language-neutral, platform-neutral, extensible mechanism for serializing structured data.
MACS 1.4.2-1-IGB-gcc-4.9.4-Python-2.7.13 Model-based Analysis of ChIP-Seq (MACS) on short reads sequencers such as Genome Analyzer (Illumina / Solexa). MACS empirically models the length of the sequenced ChIP fragments, which tends to be shorter than sonication or library construction size estimates, and uses it to improve the spatial resolution of predicted binding sites. MACS also uses a dynamic Poisson distribution to effectively capture local biases in the genome sequence, allowing for more sensitive and robust prediction.
nodejs 9.9.0-IGB-gcc-4.9.4 Node.js is a platform built on Chromes JavaScript runtime for easily building fast, scalable network applications. Node.js uses an event-driven, non-blocking I/O model that makes it lightweight and efficient, perfect for data-intensive real-time applications that run across distributed devices.
pgmpy 20180320-IGB-gcc-4.9.4-Python-3.6.1 pgmpy is a python library for working with Probabilistic Graphical Models.
libsodium 1.0.13-IGB-gcc-4.9.4 Sodium is a modern, easy-to-use software library for encryption, decryption, signatures, password hashing and more.
sparsehash 2.0.3-IGB-gcc-4.9.4 This directory contains several hash-map implementations, similar inAPI to SGIs hash_map class, but with different performance characteristics.
CUnit 2.1-3-IGB-gcc-4.9.4 CUnit is a lightweight system for writing, administering, and running unit tests in C. It provides C programmers a basic testing functionality with a flexible variety of user interfaces.
expat 2.2.0-IGB-gcc-4.9.4 Expat is an XML parser library written in C. It is a stream-oriented parser in which an application registers handlers for things the parser might find in the XML document (like start tags) - Homepage: http://expat.sourceforge.net/
Cufflinks 2.2.1
2.2.1-IGB-gcc-4.9.4-b4fa050
Transcript assembly, differential expression, and differential regulation for RNA-Seq
deep_q_rl 20160603-IGB-gcc-4.9.4-Python-2.7.13 This package provides a Lasagne/Theano-based implementation of the deep Q-learning algorithm described in:Playing Atari with Deep Reinforcement Learning Volodymyr Mnih, Koray Kavukcuoglu, David Silver, Alex Graves, Ioannis Antonoglou, Daan Wierstra, Martin RiedmillerandMnih, Volodymyr, et al. "Human-level control through deep reinforcement learning." Nature 518.7540 (2015): 529-533.
rclone 1.41 Rclone is a command line program to sync files and directories to and from different cloud storage
LibTIFF .4.0.7-IGB-gcc-4.9.4 tiff: Library and tools for reading and writing TIFF data files
jupyter 1.0.0-IGB-gcc-4.9.4-Python-3.6.1 Project Jupyter exists to develop open-source software, open-standards, and services for interactive computing across dozens of programming languages.
SRA-Toolkit 2.8.2-1 The NCBI SRA Toolkit enables reading (dumping) of sequencing files from the SRA database and writing (loading) files into the .sra format - Homepage: http://trace.ncbi.nlm.nih.gov/Traces/sra/sra.cgi?view=std
XZ .5.2.3-IGB-gcc-4.9.4 xz: XZ utilities
shapeit 2.20 SHAPEIT is a fast and accurate method for estimation of haplotypes (aka phasing) from genotype or sequencing data.
RSEM 1.3.0-IGB-gcc-4.9.4 RNA-Seq by Expectation-Maximization
GObject-Introspection .1.49.1-IGB-gcc-4.9.4-Python-2.7.13
.1.49.1-IGB-gcc-4.9.4-Python-3.6.1
GObject introspection is a middleware layer between C libraries (using GObject) and language bindings. The C library can be scanned at compile time and generate a metadata file, in addition to the actual native C library. Then at runtime, language bindings can read this metadata and automatically provide bindings to call into the C library.
Cython 0.27.3-IGB-gcc-4.9.4-Python-2.7.13 Cython is an optimising static compiler for both the Python programming language and the extended Cython programming language (based on Pyrex). It makes writing C extensions for Python as easy as Python itself.
xgboost 0.80-IGB-gcc-4.9.4-Python-3.6.1 XGBoost is an optimized distributed gradient boosting library designed to be highly efficient, flexible and portable. It implements machine learning algorithms under the Gradient Boosting framework.
TASSEL 5.2.28-Java-1.8.0_121 While TASSEL has changed considerably since its initial public release in 2001, its primary function continues to be providing tools to investigate the relationship between phenotypes and genotypes
MetaBAT 2.12.1 MetaBAT, an efficient tool for accurately reconstructing single genomes from complex microbial communities
BS-Snper 20170222-IGB-gcc-4.9.4-Perl-5.24.1 BS-SNPer is an ultrafast and memory-efficient package, a program for BS-Seq variation detection from alignments in standard BAM/SAM format using approximate Bayesian modeling.
pbzip2 1.1.13-IGB-gcc-4.9.4 PBZIP2 is a parallel implementation of the bzip2 block-sorting file compressor that uses pthreads and achieves near-linear speedup on SMP machines.
RGT 0.11.3-IGB-gcc-4.9.4-Python-2.7.13 Regulatory Genomics Toolbox (RGT) is an open source python library for analysis of regulatory genomics. RGT is programmed in an oriented object fashion and its core classes provide functionality for handling regulatory genomics data.
KAT 2.4.1-IGB-gcc-4.9.4 KAT is a suite of tools that analyse jellyfish hashes or sequence files (fasta or fastq) using kmer counts.
VICSIN 0.5-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
0.5.1-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
0.5.2-IGB-gcc-4.9.4-Perl-5.24.1-Python-2.7.13
VICSIN = Viral, Integrative, and Conjugative Sequence Identification and Networking
ScaLAPACK .2.0.2-gompi-4.9.4-OpenBLAS-0.2.19-LAPACK-3.7.0 The ScaLAPACK (or Scalable LAPACK) library includes a subset of LAPACK routines redesigned for distributed memory MIMD parallel computers. - Homepage: http://www.netlib.org/scalapack/
Clustal-Omega 1.2.4-IGB-gcc-4.9.4 Clustal Omega is a multiple sequence alignment program for proteins. It produces biologically meaningful multiple sequence alignments of divergent sequences. Evolutionary relationships can be seen via viewing Cladograms or Phylograms - Homepage: http://www.clustal.org/omega/
pylearn2 20170525-IGB-gcc-4.9.4-Python-2.7.13 Pylearn2 is a library designed to make machine learning research easy. - Homepage: https://github.com/lisa-lab/pylearn2
GMP .6.1.2-IGB-gcc-4.9.4 GMP is a free library for arbitrary precision arithmetic, operating on signed integers, rational numbers, and floating point numbers. - Homepage: http://gmplib.org/
FEELnc 20180117-IGB-gcc-4.9.4 This document is intended to give a technical description of the FEELnc pipeline in order to annotate long non-coding RNAs (lncRNAs) based on reconstructed transcripts from RNA-seq data (either with or without a reference genome).
numactl .2.0.11-GCC-4.9.4-2.28 The numactl program allows you to run your application program on specific cpus and memory nodes.It does this by supplying a NUMA memory policy to the operating system before running your program.The libnuma library provides convenient ways for you to add NUMA memory policies into your own program. - Homepage: http://oss.sgi.com/projects/libnuma/
cairo 1.14.8-IGB-gcc-4.9.4 Cairo is a 2D graphics library with support for multiple output devices. Currently supported output targets include the X Window System (via both Xlib and XCB), Quartz, Win32, image buffers, PostScript, PDF, and SVG file output. Experimental backends include OpenGL, BeOS, OS/2, and DirectFB - Homepage: http://cairographics.org
GLib 2.49.5-IGB-gcc-4.9.4 GLib is one of the base libraries of the GTK+ project - Homepage: http://www.gtk.org/
Tk .8.6.6-IGB-gcc-4.9.4 Tk is an open source, cross-platform widget toolchain that provides a library of basic elements for building a graphical user interface (GUI) in many different programming languages. - Homepage: http://www.tcl.tk/
Lasagne 20170606-IGB-gcc-4.9.4-Python-2.7.13 Lasagne is a lightweight library to build and train neural networks in Theano. - Homepage: http://lasagne.readthedocs.io/en/latest/index.html
libgpuarray 0.6.5-IGB-gcc-4.9.4 Make a common GPU ndarray(n dimensions array) that can be reused by all projects that is as future proof as possible, while keeping it easy to use for simple need/quick test. - Homepage: http://deeplearning.net/software/libgpuarray/
Pango .1.40.6-IGB-gcc-4.9.4 Pango is a library for laying out and rendering of text, with an emphasis on internationalization.Pango can be used anywhere that text layout is needed, though most of the work on Pango so far has been done in thecontext of the GTK+ widget toolkit. Pango forms the core of text and font handling for GTK+-2.x. - Homepage: http://www.pango.org/
nettle 3.3-IGB-gcc-4.9.4 Nettle is a cryptographic library that is designed to fit easily in more or less any context: In crypto toolkits for object-oriented languages (C++, Python, Pike, ...), in applications like LSH or GNUPG, or even in kernel space.
ior 3.0.1-IGB-gcc-4.9.4 Parallel filesystem I/O benchmark
RcppGSL 0.3.2-IGB-gcc-4.9.4-R-3.3.3 Rcpp integration for GNU GSL vectors and matrices The GNU Scientific Library (or GSL) is a collection of numerical routines for scientific computing. It is particularly useful for C and C++ programs as it provides a standard C interface to a wide range of mathematical routines. There are over 1000 functions in total with an extensive test suite. The RcppGSL package provides an easy-to-use interface between GSL data structures and R using concepts from Rcpp which is itself a package that eases the interfaces between R and C++. This package also serves as a prime example of how to build a package that uses Rcpp to connect to another third-party library. The autoconf script, inline plugin and example package can all be used as a stanza to write a similar package against another library.
help2man .1.47.4
.1.47.4-GCCcore-4.9.4
.1.47.4-GCCcore-7.3.0
help2man produces simple manual pages from the --help and --version output of other commands.
breseq 0.31.0-IGB-gcc-4.9.4 is a computational pipeline for the analysis of short-read re-sequencing data (e.g. Illumina, 454, IonTorrent, etc.). It uses reference-based alignment approaches to predict mutations in a sample relative to an already sequenced genome.
Tensorflow-GPU 1.2.1-IGB-gcc-4.9.4-Python-3.6.1
1.5.1-IGB-gcc-4.9.4-Python-3.6.1
An open-source software library for Machine Intelligence
rosetta 2017.52-IGB-gcc-4.9.4 The Rosetta software suite includes algorithms for computational modeling and analysis of protein structures.
bzip2 1.0.6-IGB-gcc-4.9.4 bzip2 is a freely available, patent free, high-quality data compressor. It typically compresses files to within 10% to 15% of the best available techniques (the PPM family of statistical compressors), whilst being around twice as fast at compression and six times faster at decompression. - Homepage: http://www.bzip.org/
seqan 2.3.2-IGB-gcc-4.9.4 SeqAn is an open source C++ library of efficient algorithms and data structures for the analysis of sequences with the focus on biological data
GeneMark-ES 4.33-IGB-gcc-4.9.4-Perl-5.24.1
4.33-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
Novel genomes can be analyzed by the program GeneMark-ES utilizing unsupervised training.
numpy 1.14.1-IGB-gcc-4.9.4-Python-3.6.1 NumPy is the fundamental package for scientific computing with Python. It contains among other things: a powerful N-dimensional array object, sophisticated (broadcasting) functions, tools for integrating C/C++ and Fortran code, useful linear algebra, Fourier transform, and random number capabilities. Besides its obvious scientific uses, NumPy can also be used as an efficient multi-dimensional container of generic data. Arbitrary data-types can be defined. This allows NumPy to seamlessly and speedily integrate with a wide variety of databases.
PANDAseq 2.11-IGB-gcc-4.9.4 PANDAseq assembles Illumina Solexa overlapping pair-end reads. - Homepage: https://github.com/neufeld/pandaseq
augustus 3.2.3-IGB-gcc-4.9.4 AUGUSTUS is a program that predicts genes in eukaryotic genomic sequences. - Homepage: http://bioinf.uni-greifswald.de/augustus/
TMHMM 2.0c-IGB-gcc-4.9.4 Transmembrane helices in proteins
pfamscan 1.6-IGB-gcc-4.9.4-Perl-5.24.1 This readme should help you get started with "pfam_scan.pl", which is for usewith the HMMER3 version of HMMER.
loupe 2.1.1 Loupe is a genome browser designed to visualize the Linked-Read data produced by the 10x Chromium Platform. Loupe is named for a jewelers loupe, which is used to inspect gems.
MariaDB 10.1.31-IGB-gcc-4.9.4
5.5.58-IGB-gcc-4.9.4
MariaDB An enhanced, drop-in replacement for MySQL.
geneclass 2.0 GeneClass2 is a program employing multilocus genotypes to select or exclude populations as origins of individuals (Assignment and Migrants Detection). This is a completely rewritten new version that includes pop100gene features.
cisgenome 2.0-IGB-gcc-4.9.4 An integrated tool for tiling array, ChIP-seq, genome and cis-regulatory element analysis
[Complete rewrite of the NASM assembler with BSD license - Homepage: http://www.tortall.net/projects/yasm/ Yasm] .1.3.0-IGB-gcc-4.9.4
1.3.0-IGB-gcc-4.9.4
Yasm: Complete rewrite of the NASM assembler with BSD license - Homepage: http://www.tortall.net/projects/yasm/
BLASR 4.0.0-IGB-gcc-4.9.4 BLASR (Basic Local Alignment with Successive Refinement) rapidly maps reads to genomes by finding the highest scoring local alignment or set of local alignments between the read and the genome. Optimized for PacBios extraordinarily long reads and taking advantage of rich quality values, BLASR maps reads rapidly with high accuracy.
microbiomeutil 20110519-IGB-gcc-4.9.4 Contains ChimeraSlayer, WigeoN, and NAST-iEr
PRANK 170427-IGB-gcc-4.9.4 PRANK is a probabilistic multiple alignment program for DNA, codon and amino-acid sequences. It’s based on a novel algorithm that treats insertions correctly and avoids over-estimation of the number of deletion events. In addition, PRANK borrows ideas from maximum likelihood methods used in phylogenetics and correctly takes into account the evolutionary distances between sequences. Lastly, PRANK allows for defining a potential structure for sequences to be aligned and then, simultaneously with the alignment, predicts the locations of structural units in the sequences.
gdc-client 1.3.0-IGB-gcc-4.9.4-Python-2.7.13 The GDC Data Transfer Tool Client provides a command-line interface supporting both GDC data downloads and submissions.
Phantompeaktools-spp .1.2-IGB-gcc-4.9.4-R-3.4.1 Custom SPP for Phantompeaktools
Mako 1.0.6-IGB-gcc-4.9.4-Python-3.6.1 A super-fast templating language that borrows the best ideas from the existing templating languages
randfold 2.0.1-IGB-gcc-4.9.4 Minimum free energy of folding randomization test software
admixture 1.3.0 ADMIXTURE is a software tool for maximum likelihood estimation of individual ancestries from multilocus SNP genotype datasets. It uses the same statistical model as STRUCTURE but calculates estimates much more rapidly using a fast numerical optimization algorithm.
shortbred/beta beta
lftp 4.8.3 FTP is a sophisticated file transfer program supporting a number of network protocols (ftp, http, sftp, fish, torrent).
velvet 1.2.10-IGB-gcc-4.9.4-kmer_121 Velvet is a de novo genomic assembler specially designed for short read sequencing technologies, such as Solexa or 454, developed by Daniel Zerbino and Ewan Birney at the European Bioinformatics Institute (EMBL-EBI), near Cambridge, in the United Kingdom.
libdap .3.19.1-IGB-gcc-4.9.4 A C++ SDK which contains an implementation of DAP 2.0 and the development versions of DAP3, up to 3.4. This includes both Client- and Server-side support classes.
lbzip2 2.5-IGB-gcc-4.9.4 lbzip2 is a free, multi-threaded compression utility with support for bzip2 compressed file format.
diffReps 1.55.6-IGB-gcc-4.9.4-Perl-5.24.1 ChIP-seq is now widely used to profile the protein DNA interactions on a genome. It is of high interest to compare the differential enrichment of a histone mark or transcription factor between two contrasting conditions, such as disease vs. control. diffReps is developed to serve this purpose. It scans the whole genome using a sliding window, performing millions of statistical tests and report the significant hits. - Homepage: https://github.com/shenlab-sinai/diffreps
ConsensusCore 1.0.1-IGB-gcc-4.9.4-Python-2.7.13 ConsensusCore is a library of C++ algorithms for PacBio multiple sequence consensus that powers Quiver (Python) and ConsensusTools (.NET).
efishared beta
beta_private
devel
devlocal
prod
prod_private
RNAstructure 6.0-IGB-gcc-4.9.4 RNAstructure is a complete package for RNA and DNA secondary structure prediction and analysis. It includes algorithms for secondary structure prediction, including facility to predict base pairing probabilities.
BEDTools 2.21.0-IGB-gcc-4.9.4
2.26.0-IGB-gcc-4.9.4
The BEDTools utilities allow one to address common genomics tasks such as finding feature overlaps and computing coverage. The utilities are largely based on four widely-used file formats: BED, GFF/GTF, VCF, and SAM/BAM. - Homepage: https://github.com/arq5x/bedtools2
ArcadeLearningEnvironment 0.5.1-IGB-gcc-4.9.4-Python-2.7.13 The Arcade Learning Environment (ALE) -- a platform for AI research. - Homepage: https://github.com/mgbellemare/Arcade-Learning-Environment
ncbi-vdb 2.8.2-IGB-gcc-4.9.4 The SRA Toolkit and SDK from NCBI is a collection of tools and libraries for using data in the INSDC Sequence Read Archives. - Homepage: https://github.com/ncbi/ncbi-vdb
Gdk-Pixbuf .2.36.6-IGB-gcc-4.9.4-Python-2.7.13
.2.36.6-IGB-gcc-4.9.4-Python-3.6.1
The Gdk Pixbuf is a toolkit for image loading and pixel buffer manipulation. It is used by GTK+ 2 and GTK+ 3 to load and manipulate images. In the past it was distributed as part of GTK+ 2 but it was split off into a separate package in preparation for the change to GTK+ 3.
Trim_Galore 0.4.4-IGB-gcc-4.9.4 A wrapper tool around Cutadapt and FastQC to consistently apply quality and adapter trimming to FastQ files, with some extra functionality for MspI-digested RRBS-type (Reduced Representation Bisufite-Seq) libraries. - Homepage: http://www.bioinformatics.babraham.ac.uk/projects/trim_galore/
FreeBayes 1.1.0-IGB-gcc-4.9.4 FreeBayes is a Bayesian genetic variant detector designed to find small polymorphisms, specifically SNPs (single-nucleotide polymorphisms), indels (insertions and deletions), MNPs (multi-nucleotide polymorphisms), and complex events (composite insertion and substitution events) smaller than the length of a short-read sequencing alignment.
Prodigal 2.6.3 Fast, reliable protein-coding gene prediction for prokaryotic genomes.
pigz 2.3.4-IGB-gcc-4.9.4 pigz, which stands for parallel implementation of gzip, is a fully functional replacement for gzip that exploits multiple processors and multiple cores to the hilt when compressing data. pigz was written by Mark Adler, and uses the zlib and pthread libraries. - Homepage: http://zlib.net/pigz/
HTSlib 1.3.1-IGB-gcc-4.9.4
1.4-IGB-gcc-4.9.4
1.5-IGB-gcc-4.9.4
A C library for reading/writing high-throughput sequencing data. This package includes the utilities bgzip and tabix
AdapterRemoval 2.1.7-IGB-gcc-4.9.4 This program searches for and removes remnant adapter sequences from High-Throughput Sequencing (HTS) data and (optionally) trims low quality bases from the 3 end of reads following adapter removal.
libffi .3.2.1-IGB-gcc-4.9.4 The libffi library provides a portable, high level programming interface to various callingconventions. This allows a programmer to call any function specified by a call interface description at run-time. - Homepage: http://sourceware.org/libffi/
rpy 1.0.3-IGB-gcc-4.9.4-Python-2.7.13-R-2.15.3 RPy is a very simple, yet robust, Python interface to the R Programming Language. Itcan manage all kinds of R objects and can execute arbitrary R functionsincluding the graphic functions.
keras-rl 0.3.0-IGB-gcc-4.9.4-Python-2.7.13 keras-rl implements some state-of-the art deep reinforcement learning algorithms in Python and seamlessly integrates with the deep learning library Keras.
quickmerge 0.2-IGB-gcc-4.9.4-Python-2.7.13 quickmerge uses a simple concept to improve contiguity of genome assemblies based on long molecule sequences, often with dramatic outcomes. The program uses information from assemblies made with illumina short reads and PacBio long reads to improve contiguities of an assembly generated with PacBio long reads alone. This is counterintuitive because illumina short reads are not typically considered to cover genomic regions which PacBio long reads cannot. Although we have not evaluated this program for assemblies generated with Oxford nanopore sequences, the program should work with ONP-assemblies too.
ROSE 20150210-IGB-gcc-4.9.4-Python-2.7.13 To create stitched enhancers, and to separate super-enhancers from typical enhancers using sequencing data (.bam)
SWIG 2.0.12-IGB-gcc-4.9.4-Python-2.7.13
3.0.12-IGB-gcc-4.9.4-Python-2.7.13
3.0.12-IGB-gcc-4.9.4-Python-2.7.13-Perl-5.24.1
SWIG is a software development tool that connects programs written in C and C++ with a variety of high-level programming languages. - Homepage: http://www.swig.org/
numba 0.34.0-IGB-gcc-4.9.4-Python-2.7.13
0.34.0-IGB-gcc-4.9.4-Python-3.6.1
Numba is an Open Source NumPy-aware optimizing compiler for Python sponsored by Continuum Analytics, Inc. It uses the remarkable LLVM compiler infrastructure to compile Python syntax to machine code.
HUMAnN2 0.11.1-IGB-gcc-4.9.4-Python-3.6.1 HUMAnN is a pipeline for efficiently and accurately profiling the presence/absence and abundance of microbial pathways in a community from metagenomic or metatranscriptomic sequencing data (typically millions of short DNA/RNA reads). This process, referred to as functional profiling, aims to describe the metabolic potential of a microbial community and its members. More generally, functional profiling answers the question "What are the microbes in my community-of-interest doing (or capable of doing)?"
[GNU binary utilities - Homepage: http://directory.fsf.org/project/binutils/ binutils] .2.28
.2.28-GCCcore-4.9.4
binutils: GNU binary utilities - Homepage: http://directory.fsf.org/project/binutils/
JUnit 4.12-Java-1.8.0_121 A programmer-oriented testing framework for Java.
FFTW .3.3.6-gompi-4.9.4 FFTW is a C subroutine library for computing the discrete Fourier transform (DFT) in one or more dimensions, of arbitrary input size, and of both real and complex data. - Homepage: http://www.fftw.org
Kraken 1.0-IGB-gcc-4.9.4 Kraken is a system for assigning taxonomic labels to short DNA sequences, usually obtained through metagenomic studies. Previous attempts by other bioinformatics software to accomplish this task have often used sequence alignment or machine learning techniques that were quite slow, leading to the development of less sensitive but much faster abundance estimation programs.
MAFFT 7.310-IGB-gcc-4.9.4 MAFFT is a multiple sequence alignment program for unix-like operating systems. It offers a range of multiple alignment methods, L-INS-i (accurate; for alignment of <∼200 sequences), FFT-NS-2 (fast; for alignment of <∼10,000 sequences), etc. - Homepage: http://mafft.cbrc.jp/alignment/software/
FastQC 0.11.5-IGB-gcc-4.9.4-Java-1.8.0_121
0.11.5-IGB-gcc-4.9.4-Java-1.8.0_152
FastQC is a quality control application for high throughput sequence data. It reads in sequence data in a variety of formats and can either provide an interactive application to review the results of several different QC checks, or create an HTML based report which can be integrated into a pipeline.
pplacer 1.1.alpha19 Pplacer places query sequences on a fixed reference phylogenetic tree to maximize phylogenetic likelihood or posterior probability according to a reference alignment. Pplacer is designed to be fast, to give useful information about uncertainty, and to offer advanced visualization and downstream analysis.
ARCS 1.0.0-IGB-gcc-4.9.4-Perl-5.24.1 Scaffolding genome sequence assemblies using 10X Genomics GemCode/Chromium data. - Homepage: https://github.com/bcgsc/arcs
ZeroMQ 4.2.2-IGB-gcc-4.9.4 ZeroMQ looks like an embeddable networking library but acts like a concurrency framework. It gives you sockets that carry atomic messages across various transports like in-process, inter-process, TCP, and multicast. You can connect sockets N-to-N with patterns like fanout, pub-sub, task distribution, and request-reply. It is fast enough to be the fabric for clustered products. Its asynchronous I/O model gives you scalable multicore applications, built as asynchronous message-processing tasks. It has a score of language APIs and runs on most operating systems.
PROJ .4.9.3-IGB-gcc-4.9.4 Program proj is a standard Unix filter function which converts geographic longitude and latitude coordinates into cartesian coordinates - Homepage: http://trac.osgeo.org/proj/
freetype 2.7.1-IGB-gcc-4.9.4 FreeType 2 is a software font engine that is designed to be small, efficient, highly customizable, and portable while capable of producing high-quality output (glyph images). It can be used in graphics libraries, display servers, font conversion tools, text image generation tools, and many other products as well. - Homepage: http://freetype.org
aspera 3.7.6 Aspera’s unwavering mission is to create the next-generation software technologies that move the world’s data at maximum speed, regardless of file size, transfer distance and network conditions.
libcerf 1.5-IGB-gcc-4.9.4 libcerf is a self-contained numeric library that provides an efficient and accurate implementation of complex error functions, along with Dawson, Faddeeva, and Voigt functions. - Homepage: http://apps.jcns.fz-juelich.de/doku/sc/libcerf
ATK .2.24.0-IGB-gcc-4.9.4-Python-2.7.13
.2.24.0-IGB-gcc-4.9.4-Python-3.6.1
ATK provides the set of accessibility interfaces that are implemented by other toolkits and applications. Using the ATK interfaces, accessibility tools have full access to view and control running applications.
seqtk 1.2-IGB-gcc-4.9.4 Seqtk is a fast and lightweight tool for processing sequences in the FASTA or FASTQ format. It seamlessly parses both FASTA and FASTQ files which can also be optionally compressed by gzip. - Homepage: https://github.com/lh3/seqtk/
Canu 1.4-IGB-gcc-4.9.4-Perl-5.24.1
1.5-IGB-gcc-4.9.4-Perl-5.24.1
1.6-IGB-gcc-4.9.4-Perl-5.24.1
1.7-IGB-gcc-4.9.4-Perl-5.24.1
1.7.1-IGB-gcc-4.9.4-Perl-5.24.1
Canu is a fork of the Celera Assembler, designed for high-noise single-molecule sequencing (such as the PacBio RS II or Oxford Nanopore MinION).
pybedtools 0.7.10-IGB-gcc-4.9.4-Python-3.6.1 pybedtools is a Python package that wraps BEDTools, so you will need both installed.
libpciaccess .0.13.4-IGB-gcc-4.9.4 Generic PCI access library.
Anaconda2 4.3.1 Built to complement the rich, open source Python community,the Anaconda platform provides an enterprise-ready data analytics platform that empowers companies to adopt a modern open data science analytics architecture. - Homepage: https://www.continuum.io/anaconda-overview
SoX 14.4.2-IGB-gcc-4.9.4 Sound eXchange, the Swiss Army knife of audio manipulation
Spine 0.2.1-IGB-gcc-4.9.4 Spine identifies a core genome from input genomic sequences. Sequences are aligned using Nucmer and regions found to be in common between all or a user-defined subset of genomes will be returned.
GUIDANCE 2.02-IGB-gcc-4.9.4-Perl-5.24.1 GUIDANCE is meant to be used for weighting, filtering or masking unreliably aligned positions in sequence alignments before subsequent analysis. For example, align codon sequences (nucleotide sequences that code for proteins) using PAGAN, remove columns with low GUIDANCE scores, and use the remaining alignment to infer positive selection using the branch-site dN/dS test. Other analyses where GUIDANCE filtering could be useful include phylogeny reconstruction, reconstruction of the history of specific insertion and deletion events, inference of recombination events, etc. - Homepage: http://guidance.tau.ac.il/ver2/
lzo .2.10-IGB-gcc-4.9.4 Portable lossless data compression library
coreutils 8.28-IGB-gcc-4.9.4 The GNU Core Utilities are the basic file, shell and text manipulation utilities of the GNU operating system.These are the core utilities which are expected to exist on every operating system.
SOAPdenovo-Trans 1.03 SOAPdenovo-Trans is a de novo transcriptome assembler basing on the SOAPdenovo framework, adapt to alternative splicing and different expression level among transcripts.The assembler provides a more accurate, complete and faster way to construct the full-length transcript sets.
Theano 0.9.0-IGB-gcc-4.9.4-Python-2.7.13 Theano is a Python library that allows you to define, optimize,and evaluate mathematical expressions involving multi-dimensional arrays efficiently. - Homepage: http://deeplearning.net/software/theano
nanopolish 0.10.1-IGB-gcc-4.9.4
0.6.0-IGB-gcc-4.9.4
0.7.1-IGB-gcc-4.9.4
0.7.1-IGB-gcc-4.9.4-159d92b
0.8.3-IGB-gcc-4.9.4
0.8.5-IGB-gcc-4.9.4
0.9.0-IGB-gcc-4.9.4
Software package for signal-level analysis of Oxford Nanopore sequencing data.
netCDF-Fortran .4.4.1-IGB-gcc-4.9.4
4.4.1-IGB-gcc-4.9.4
NetCDF (network Common Data Form) is a set of software libraries and machine-independent data formats that support the creation, access, and sharing of array-oriented scientific data.
BCFtools 1.4-IGB-gcc-4.9.4
1.5-IGB-gcc-4.9.4
1.7-IGB-gcc-4.9.4
BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF
epic 0.2.9-IGB-gcc-4.9.4-Python-2.7.13 epic is a software package for finding medium to diffusely enriched domains in chip-seq data. It is a fast, parallel and memory-efficient implementation of the incredibly popular SICER algorithm.
Java 1.8.0_121
1.8.0_152
Java Platform, Standard Edition (Java SE) lets you develop and deploy Java applications on desktops and servers. - Homepage: http://java.com/
Jellyfish 1.1.12-IGB-gcc-4.9.4
2.2.6-IGB-gcc-4.9.4
Jellyfish is a tool for fast, memory-efficient counting of k-mers in DNA. - Homepage: http://www.genome.umd.edu/jellyfish.html
poretools 0.6.0-IGB-gcc-4.9.4-Python-2.7.13 a toolkit for working with nanopore sequencing data from Oxford Nanopore. - Homepage: https://github.com/arq5x/poretools
BreakSeq2 2.2-IGB-gcc-4.9.4-Python-2.7.13 Ultrafast and accurate nucleotide-resolution analysis of structural variants - Homepage: http://bioinform.github.io/breakseq2/
metaphlan2 2.6.0-IGB-gcc-4.9.4-Python-3.6.1
2.7.6-IGB-gcc-4.9.4-Python-2.7.13
MetaPhlAn is a computational tool for profiling the composition of microbial communities (Bacteria, Archaea, Eukaryotes and Viruses) from metagenomic shotgun sequencing data (i.e. not 16S) with species-level. With the newly added StrainPhlAn module, it is now possible to perform accurate strain-level microbial profiling.
fontconfig 2.12.1-IGB-gcc-4.9.4 Fontconfig is a library designed to provide system-wide font configuration, customization andapplication access. - Homepage: http://www.freedesktop.org/software/fontconfig
Bowtie 1.2.0-IGB-gcc-4.9.4 Bowtie is an ultrafast, memory-efficient short read aligner.It aligns short DNA sequences (reads) to the human genome. - Homepage: http://bowtie-bio.sourceforge.net/index.shtml
Tensorflow 1.2.1-IGB-gcc-4.9.4-Python-2.7.13 An open-source software library for Machine Intelligence
Autoconf .2.69
.2.69-IGB-gcc-4.9.4
Autoconf is an extensible package of M4 macros that produce shell scripts to automatically configure software source code packages. These scripts can adapt the packages to many kinds of UNIX-like systems without manual user intervention. Autoconf creates a configuration script for a package from a template file that lists the operating system features that the package can use, in the form of M4 macro calls. - Homepage: http://www.gnu.org/software/autoconf/
FastTree 2.1.10-IGB-gcc-4.9.4 FastTree infers approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences. FastTree can handle alignments with up to a million of sequences in a reasonable amount of time and memory.
fdupes 1.6.1-IGB-gcc-4.9.4 FDUPES is a program for identifying duplicate files residingwithin specified directories.
CMake .3.12.1-IGB-gcc-4.9.4
.3.7.2-IGB-gcc-4.9.4
CMake, the cross-platform, open-source build system. CMake is a family of tools designed to build, test and package software. - Homepage: http://www.cmake.org
gperf 3.1-IGB-gcc-4.9.4 GNU gperf is a perfect hash function generator. For a given list of strings, it produces a hash function and hash table, in form of C or C++ code, for looking up a value depending on the input string. The hash function is perfect, which means that the hash table has no collisions, and the hash table lookup needs a single string comparison only.
ADOL-C 2.6.3-IGB-gcc-4.9.4 ADOL-C is an open-source package for the automatic differentiation of C and C++ programs.
zlib .1.2.11
.1.2.11-GCCcore-4.9.4
.1.2.11-IGB-gcc-4.9.4
zlib is designed to be a free, general-purpose, legally unencumbered -- that is, not covered by any patents -- lossless data-compression library for use on virtually any computer hardware and operating system. - Homepage: http://www.zlib.net/
PITA 6-IGB-gcc-4.9.4 The PITA executable allows you to identify and score microRNA targets on UTRs.
Krona 2.7-IGB-gcc-4.9.4-Perl-5.24.1 Interactively explore metagenomes and more from a web browser.
pal2nal 14-IGB-gcc-4.9.4 PAL2NAL is a program that converts a multiple sequence alignment of proteins and the corresponding DNA (or mRNA) sequences into a codon alignment.
Unicycler 0.4.3-IGB-gcc-4.9.4-Python-3.6.1
0.4.4-IGB-gcc-4.9.4-Python-3.6.1
Unicycler is an assembly pipeline for bacterial genomes. It can assemble Illumina-only read sets where it functions as a SPAdes-optimiser. It can also assembly long-read-only sets (PacBio or Nanopore) where it runs a miniasm+Racon pipeline. For the best possible assemblies, give it both Illumina reads and long reads, and it will conduct a hybrid assembly.
HOMER 4.9.1-IGB-gcc-4.9.4-Perl-5.24.1 HOMER (Hypergeometric Optimization of Motif EnRichment) is a suite of tools for Motif Discovery and ChIP-Seq analysis. It is a collection of command line programs for unix-style operating systems written in mostly perl and c++. Homer was primarily written as a de novo motif discovery algorithm that is well suited for finding 8-12 bp motifs in large scale genomics data.
OpenBLAS .0.2.19-GCC-4.9.4-2.28-LAPACK-3.7.0
0.2.19-GCC-4.9.4-2.28-LAPACK-3.7.0
OpenBLAS is an optimized BLAS library based on GotoBLAS2 1.13 BSD version. - Homepage: http://xianyi.github.com/OpenBLAS/
gtool 0.7.5 GTOOL is a program for transforming sets of genotype data for use with the programs SNPTEST and IMPUTE.
sharutils 4.15.2-IGB-gcc-4.9.4 GNU shar makes so-called shell archives out of many files, preparing them for transmission by electronic mail services, while unshar helps unpacking shell archives after reception.
graphlan 6ca8735-IGB-gcc-4.9.4-Python-2.7.13 GraPhlAn is a software tool for producing high-quality circular representations of taxonomic and phylogenetic trees. It focuses on concise, integrative, informative, and publication-ready representations of phylogenetically- and taxonomically-driven investigation.
DISCOVARdenovo 52488-IGB-gcc-4.9.4 DISCOVAR de novo can generate de novo assemblies for both large and small genomes. It currently does not call variants.
Gurobi 7.5.2 The Gurobi Optimizer was designed from the ground up to be the fastest, most powerful solver available for your LP, QP, QCP, and MIP (MILP, MIQP, and MIQCP) problems.
pixman 0.34.0-IGB-gcc-4.9.4 Pixman is a low-level software library for pixel manipulation, providing features such as imagecompositing and trapezoid rasterization. Important users of pixman are the cairo graphics library and the X server. - Homepage: http://www.pixman.org/
ViennaRNA 2.4.2-IGB-gcc-4.9.4 The ViennaRNA Package consists of a C code library and several stand-alone programs for the prediction and comparison of RNA secondary structures.
FALCON_unzip 0.4.0-IGB-gcc-4.9.4-Python-2.7.13 FALCON-Unzip contains the modules that works with FALCON for full diploid assembly (representing haplotype specific contigs as "haplotigs" as assembly output).
FALCON 1.8.8-IGB-gcc-4.9.4-Python-2.7.13 FALCON is a diploid aware genome assembler designed for Pacific Biosciences long read data.
xorg-macros .1.19.0-IGB-gcc-4.9.4 X.org macros utilities.
scrappie 1.3.0-IGB-gcc-4.9.4 Scrappie is a technology demonstrator for the Oxford Nanopore Research Algorithms group.
flexbar 3.0.3-IGB-gcc-4.9.4 The program Flexbar preprocesses high-throughput sequencing data efficiently. It demultiplexes barcoded runs and removes adapter sequences. Moreover, trimming and filtering features are provided.
ImageMagick 7.0.5-5-IGB-gcc-4.9.4 ImageMagick is a software suite to create, edit, compose, or convert bitmap images - Homepage: http://www.imagemagick.org/
nextflow 0.25.7-Java-1.8.0_121
0.26.3-Java-1.8.0_152
Nextflow enables scalable and reproducible scientific workflows using software containers. It allows the adaptation of pipelines written in the most common scripting languages.
AGEnt 0.2.1-IGB-gcc-4.9.4 AGEnt performs in silico subtractive hybridization of core genome sequences, such as those produced by Spine, against a query genomic sequence to identify accessory genomic sequences (AGEs) in the query genome. Sequences are aligned using Nucmer, outputting sequences and sequence characteristics of those regions in the query genome that are not found in the core genome. If gene coordinate information is provided, a list of accessory genes in the query genome will also be output.
Bowtie2 2.1.0-IGB-gcc-4.9.4
2.3.1-IGB-gcc-4.9.4
2.3.2-IGB-gcc-4.9.4
Bowtie 2 is an ultrafast and memory-efficient tool for aligning sequencing reads to long reference sequences. It is particularly good at aligning reads of about 50 up to 100s or 1,000s of characters, and particularly good at aligning to relatively long (e.g. mammalian) genomes. Bowtie 2 indexes the genome with an FM Index to keep its memory footprint small: for the human genome, its memory footprint is typically around 3.2 GB. Bowtie 2 supports gapped, local, and paired-end alignment modes. - Homepage: http://bowtie-bio.sourceforge.net/bowtie2/index.shtml
BLAT 3.5-IGB-gcc-4.9.4 BLAT on DNA is designed to quickly find sequences of 95% and greater similarity of length 25 bases or more.
blobtools 0.9.19.6-IGB-gcc-4.9.4-Python-2.7.13 Application for the visualisation of (draft) genome assemblies using TAGC (Taxon-annotated Gc-Coverage) plots - Homepage: https://github.com/DRL/blobtools
fast5 0.6.2-IGB-gcc-4.9.4
0.6.3-IGB-gcc-4.9.4
0.6.5-IGB-gcc-4.9.4
A lightweight C++ library for accessing Oxford Nanopore Technologies sequencing data.
medaka 0.1.0-IGB-gcc-4.9.4-Python-3.6.1 Medaka demonstrates a framework for error correcting sequencing data, particularly aimed at nanopore sequencing. Tools are provided for both training and inference. The code exploits the keras deep learning library.
OpenMPI 2.1.0-GCC-4.9.4-2.28 The Open MPI Project is an open source MPI-2 implementation.
Automake .1.15
.1.15-IGB-gcc-4.9.4
Automake: GNU Standards-compliant Makefile generator
Bismark 0.17.0-IGB-gcc-4.9.4-Perl-5.24.1
0.18.1-IGB-gcc-4.9.4-Perl-5.24.1
A tool to map bisulfite converted sequence reads and determine cytosine methylation states - Homepage: http://www.bioinformatics.babraham.ac.uk/projects/bismark/
FASTX-Toolkit 0.0.14-IGB-gcc-4.9.4 The FASTX-Toolkit is a collection of command line tools for Short-Reads FASTA/FASTQ files preprocessing. - Homepage: http://hannonlab.cshl.edu/fastx_toolkit/
jemalloc 5.0.1-IGB-gcc-4.9.4 jemalloc is a general purpose malloc(3) implementation that emphasizes fragmentation avoidance and scalable concurrency support.
TensorFlowModels 1.11-IGB-gcc-4.9.4-Python-3.6.1
20171113-IGB-gcc-4.9.4-Python-3.6.1
This repository contains a number of different models implemented in TensorFlow:
HDF5 1.8.18-IGB-gcc-4.9.4 HDF5 is a unique technology suite that makes possible the management of extremely large and complex data collections.
libxml2 2.9.4-IGB-gcc-4.9.4 Libxml2 is the XML C parser and toolchain developed for the Gnome project (but usable outside of the Gnome platform). - Homepage: http://xmlsoft.org/
GTK+ 2.24.31-IGB-gcc-4.9.4-Python-2.7.13
2.24.31-IGB-gcc-4.9.4-Python-3.6.1
The GTK+ 2 package contains libraries used for creating graphical user interfaces for applications.
libevent .2.1.8-IGB-gcc-4.9.4 The libevent API provides a mechanism to execute a callback function when a specific event occurs on a file descriptor or after a timeout has been reached. Furthermore, libevent also support callbacks due to signals or regular timeouts. - Homepage: http://libevent.org/
cdbfasta 20170316-IGB-gcc-4.9.4 CDB (Constant DataBase) indexing and retrieval tools for FASTA files
racon 0.5.0-IGB-gcc-4.9.4-Python-2.7.13
0.5.0-IGB-gcc-4.9.4-Python-3.6.1
Racon is intended as a standalone consensus module to correct raw contigs generated by rapid assembly methods which do not include a consensus step, such as Miniasm.The goal of Racon is to generate genomic consensus which is of similar or better quality compared to the output generated by assembly methods which employ both error correction and consensus steps, while providing a speedup of several times compared to those methods.
snpEff 4.3o-Java-1.8.0_121 SnpEff is a variant annotation and effect prediction tool. It annotates and predicts the effects of genetic variants (such as amino acid changes).
cuDNN 5.1-IGB-gcc-4.9.4-CUDA-8.0.61
6.0-IGB-gcc-4.9.4-CUDA-8.0.61
7.0.5-IGB-gcc-4.9.4-CUDA-9.0.176
7.1.4-IGB-gcc-4.9.4-CUDA-9.0.176
The NVIDIA CUDA Deep Neural Network library (cuDNN) is a GPU-accelerated library of primitives for deep neural networks.
IGB-gcc .4.9.4 GNU Compiler Collection (GCC) based compiler toolchain, including OpenMPI for MPI support, OpenBLAS (BLAS and LAPACK support), FFTW and ScaLAPACK.
beagle 03Jul18.40b-Java-1.8.0_152 Beagle is a software package for phasing genotypes and for imputing ungenotyped markers. Version 5.0 has new, fast algorithms for genotype phasing and imputation.
prokka 1.12-IGB-gcc-4.9.4-Perl-5.24.1
1.13-IGB-gcc-4.9.4-Perl-5.24.1
Whole genome annotation is the process of identifying features of interest in a set of genomic DNA sequences, and labelling them with useful information. Prokka is a software tool to annotate bacterial, archaeal and viral genomes quickly and produce standards-compliant output files.
libgd .2.2.4-IGB-gcc-4.9.4 GD is an open source code library for the dynamic creation of images by programmers. - Homepage: http://libgd.bitbucket.org/
EasyBuild 3.5.3
3.6.0
3.6.2
EasyBuild is a software build and installation frameworkwritten in Python that allows you to install software in a structured,repeatable and robust way.
parallel 20170622-IGB-gcc-4.9.4 parallel: GNU parallel is a shell tool for executing jobs in parallel using one or more computers.
GenomicConsensus 3.0.2-IGB-gcc-4.9.4-Python-2.7.13 The GenomicConsensus package provides the variantCaller tool, which allows you to apply the Quiver or Arrow algorithm to mapped PacBio reads to get consensus and variant calls.
AdmixTools 1.0.1-IGB-gcc-4.9.4 The ADMIXTOOLS package implements 5 methods described in Patterson et al. (2012) Ancient Admixture in Human History. Details of the methods and algorithm can be found in this paper.
efidb ip62
ip63
ip64
ip65
ip66
ip66_private
ip67
ip68
ip69
R 2.15.3-IGB-gcc-4.9.4
3.1.2-IGB-gcc-4.9.4
3.2.5-IGB-gcc-4.9.4
3.3.3-IGB-gcc-4.9.4
3.4.1-IGB-gcc-4.9.4
3.4.2-IGB-gcc-4.9.4
3.5.0-IGB-gcc-4.9.4
R is a free software environment for statistical computing and graphics.
Mothur 1.38.1.1
1.39.5
1.39.5-IGB-gcc-4.9.4
Mothur is a single piece of open-source, expandable software to fill the bioinformatics needs of the microbial ecology community.
OpenPGM 5.2.122-IGB-gcc-4.9.4 OpenPGM is an open source implementation of the Pragmatic General Multicast (PGM) specification in RFC 3208 available at www.ietf.org. PGM is a reliable and scalable multicast protocol that enables receivers to detect loss, request retransmission of lost data, or notify an application of unrecoverable loss. PGM is a receiver-reliable protocol, which means the receiver is responsible for ensuring all data is received, absolving the sender of reception responsibility.
cURL .7.53.1-IGB-gcc-4.9.4 libcurl is a free and easy-to-use client-side URL transfer library, supporting DICT, FILE, FTP, FTPS, Gopher, HTTP, HTTPS, IMAP, IMAPS, LDAP, LDAPS, POP3, POP3S, RTMP, RTSP, SCP, SFTP, SMTP, SMTPS, Telnet and TFTP. libcurl supports SSL certificates, HTTP POST, HTTP PUT, FTP uploading, HTTP form based upload, proxies, cookies, user+password authentication (Basic, Digest, NTLM, Negotiate, Kerberos), file transfer resume, http proxy tunneling and more. - Homepage: http://curl.haxx.se
LittleCMS .2.8-IGB-gcc-4.9.4
2.8-IGB-gcc-4.9.4
Little CMS intends to be an OPEN SOURCE small-footprint color management engine, with special focus on accuracy and performance. - Homepage: http://www.littlecms.com/
SCons 3.0.1-IGB-gcc-4.9.4-Python-2.7.13
3.0.1-IGB-gcc-4.9.4-Python-3.6.1
SCons is a software construction tool.
valgrind 3.13.0-IGB-gcc-4.9.4 Valgrind is an instrumentation framework for building dynamic analysis tools. There are Valgrind tools that can automatically detect many memory management and threading bugs, and profile your programs in detail. You can also use Valgrind to build new tools.
GATK 3.7-Java-1.8.0_121
3.8-0-Java-1.8.0_152
3.8-1-0-Java-1.8.0_152
4.0.4.0-IGB-gcc-4.9.4-Java-1.8.0_152-Python-3.6.1
The Genome Analysis Toolkit or GATK is a software package developed at the Broad Institute to analyse next-generation resequencing data. The toolkit offers a wide variety of tools, with a primary focus on variant discovery and genotyping as well as strong emphasis on data quality assurance. Its robust architecture, powerful processing engine and high-performance computing features make it capable of taking on projects of any size.
cutadapt 1.14-IGB-gcc-4.9.4-Python-2.7.13
1.17-IGB-gcc-4.9.4-Python-3.6.1
Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads.
libtool .2.4.6
.2.4.6-IGB-gcc-4.9.4
GNU libtool is a generic library support script. Libtool hides the complexity of using shared libraries behind a consistent, portable interface. - Homepage: http://www.gnu.org/software/libtool
ncdf4 1.16-IGB-gcc-4.9.4-R-3.3.3 This package provides a high-level R interface to data files written using Unidatas netCDF library (version 4 or earlier), which are binary data files that are portable across platforms and include metadata information in addition to the data sets.
mirdeep 2.0.0.8-IGB-gcc-4.9.4 miRDeep2 is a completely overhauled tool which discovers microRNA genes by analyzing sequenced RNAs.
PICRUSt 1.1.1-IGB-gcc-4.9.4-Python-2.7.13
1.1.3-IGB-gcc-4.9.4-Python-2.7.13
PICRUSt (pronounced pie crust) is a bioinformatics software package designed to predict metagenome functional content from marker gene (e.g., 16S rRNA) surveys and full genomes.
SPAdes 3.10.1-IGB-gcc-4.9.4-Python-2.7.13
3.11.0-IGB-gcc-4.9.4-Python-2.7.13
3.11.0-IGB-gcc-4.9.4-Python-3.6.1
3.11.1-IGB-gcc-4.9.4-Python-3.6.1
SPAdes . St. Petersburg genome assembler . is intended for both standard isolates and single-cell MDA bacteria assemblies.
tabix 0.2.6-IGB-gcc-4.9.4 Generic indexer for TAB-delimited genome position files
rtg-tools 3.8.4 RTG Tools contains utilities to easily manipulate and accurately compare multiple VCF files, as well as utilities for processing other common NGS data formats.
NGS 1.3.0-IGB-gcc-4.9.4 NGS is a new, domain-specific API for accessing reads, alignments and pileups produced from Next Generation Sequencing. - Homepage: https://github.com/ncbi/ngs
NCO 4.7.2-IGB-gcc-4.9.4 manipulates and analyzes data stored in netCDF-accessible formats, including DAP, HDF4, and HDF5
nose-parameterized 0.6.0-IGB-gcc-4.9.4-Python-2.7.13 Parameterized testing with any Python test framework.
MEGAN 6.12.2-Java-1.8.0_152 MEGAN6 is a comprehensive toolbox for interactively analyzing microbiome data. All the interactive tools you need in one application.
BUSCO 3.0.1-IGB-gcc-4.9.4-Python-2.7.13 BUSCO v3 provides quantitative measures for the assessment of genome assembly, gene set, and transcriptome completeness, based on evolutionarily-informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB v9.
JasPer 1.900.1-IGB-gcc-4.9.4
2.0.10-IGB-gcc-4.9.4
The JasPer Project is an open-source initiative to provide a free software-based reference implementation of the codec specified in the JPEG-2000 Part-1 standard. - Homepage: http://www.ece.uvic.ca/~frodo/jasper/
FLAC 1.3.1-IGB-gcc-4.9.4 Programs and libraries for working with Free Lossless Audio Codec (FLAC) files.
bax2bam 20171114-IGB-gcc-4.9.4 bax2bam converts the legacy PacBio basecall format (bax.h5) into the BAMbasecall format.
HTSeq 0.9.0-IGB-gcc-4.9.4-Python-2.7.13
0.9.1-IGB-gcc-4.9.4-Python-2.7.13
A framework to process and analyze data from high-throughput sequencing (HTS) assays
ssaha_pileup 0.6-IGB-gcc-4.9.4 SSAHA2: Sequence Search and Alignment by Hashing Algorithm
GD 2.66-IGB-gcc-4.9.4-Perl-5.24.1 GD.pm - Interface to Gd Graphics Library
HISAT2 2.0.5-IGB-gcc-4.9.4 HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) against the general human population (as well as against a single reference genome). - Homepage: https://ccb.jhu.edu/software/hisat2/index.shtml
gettext .0.19.8
.0.19.8-IGB-gcc-4.9.4
GNU gettext is an important step for the GNU Translation Project, as it is an asset on which we maybuild many other steps. This package offers to programmers, translators, and even users, a well integrated set of toolsand documentation
OrthoMCL 2.0.9-IGB-gcc-4.9.4-Perl-5.24.1 OrthoMCL is a genome-scale algorithm for grouping orthologous protein sequences. - Homepage: http://orthomcl.org/
x264 .20170604-IGB-gcc-4.9.4 x264 is a free software library and application for encoding video streams into the H.264/MPEG-4 AVC compression format, and is released under the terms of the GNU GPL. - Homepage: http://www.videolan.org/developers/x264.html
MaSuRCA 3.2.3-IGB-gcc-4.9.4 MaSuRCA is whole genome assembly software. It combines the efficiency of the de Bruijn graph and Overlap-Layout-Consensus (OLC) approaches. MaSuRCA can assemble data sets containing only short reads from Illumina sequencing or a mixture of short reads and long reads (Sanger, 454, Pacbio and Nanopore).
IDR 2.0.4-IGB-gcc-4.9.4-Python-3.6.1 The IDR (Irreproducible Discovery Rate) framework is a unified approach to measure the reproducibility of findings identified from replicate experiments and provide highly stable thresholds based on reproducibility. Unlike the usual scalar measures of reproducibility, the IDR approach creates a curve, which quantitatively assesses when the findings are no longer consistent across replicates. In laymans terms, the IDR method compares a pair of ranked lists of identifications (such as ChIP-seq peaks).
unanimity 20180307-IGB-gcc-4.9.4 C++ library and its applications to generate and process accurate consensus sequences
shortbred/devlocal devlocal
Bison .3.0.4
.3.0.4-GCCcore-4.9.4
Bison is a general-purpose parser generator that converts an annotated context-free grammarinto a deterministic LR or generalized LR (GLR) parser employing LALR(1) parser tables. - Homepage: http://www.gnu.org/software/bison
atactk 0.1.6-IGB-gcc-4.9.4-Python-2.7.13 a toolkit for ATAC-seq data
MATLAB-python 2017b-IGB-gcc-4.9.4-Python-3.6.1 The MATLAB Engine API for Python provides a package for Python to call MATLAB as a computational engine. The engine supports the reference implementation (CPython) for Python versions 2.7, 3.5, and 3.6.
Szip .2.1.1-IGB-gcc-4.9.4 Szip compression software, providing lossless compression of scientific data - Homepage: http://www.hdfgroup.org/doc_resource/SZIP/
TULIP 20170513-IGB-gcc-4.9.4-Perl-5.24.1 Tulipseed takes as input alignments files of long reads to sparse short seeds, and outputs a graph and scaffold structures. Tulipbulb adds long read sequencing data to these.
Autotools .20150215
.20150215-IGB-gcc-4.9.4
This bundle collect the standard GNU build tools: Autoconf, Automake and libtool
LLVM 4.0.1-IGB-gcc-4.9.4
6.0.0-IGB-gcc-4.9.4
The LLVM Core libraries provide a modern source- and target-independent optimizer, along with code generation support for many popular CPUs (as well as some less common ones!) These libraries are built around a well specified code representation known as the LLVM intermediate representation ("LLVM IR"). The LLVM Core libraries are well documented, and it is particularly easy to invent your own language (or port an existing compiler) to use LLVM as an optimizer and code generator.
albacore 2.0.2-IGB-gcc-4.9.4-Python-3.6.1
2.1.10-IGB-gcc-4.9.4-Python-3.6.1
2.3.1-IGB-gcc-4.9.4-Python-3.6.1
Local basecalling for MinKNOW
StringTie 1.3.3-IGB-gcc-4.9.4 StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts. - Homepage: http://ccb.jhu.edu/software/stringtie/
CD-HIT 4.6.6-IGB-gcc-4.9.4 CD-HIT is a very widely used program for clustering and comparing protein or nucleotide sequences. - Homepage: http://weizhong-lab.ucsd.edu/cd-hit/
impute2 2.3.2 IMPUTE2 is freely available for academic use. To see rules for non-academic use, please read the LICENCE file, which is included with each software download.
cellranger 2.1.0
2.1.1
Cell Ranger is a set of analysis pipelines that process Chromium single cell 3 RNA-seq output to align reads, generate gene-cell matrices and perform clustering and gene expression analysis.
BLAST+ 2.6.0-IGB-gcc-4.9.4
2.7.1-IGB-gcc-4.9.4
2.8.0-IGB-gcc-4.9.4-alpha
Basic Local Alignment Search Tool, or BLAST, is an algorithm for comparing primary biological sequence information, such as the amino-acid sequences of different proteins or the nucleotides of DNA sequences.
EMBOSS 6.6.0-IGB-gcc-4.9.4-Java-1.8.0_121 EMBOSS, The European Molecular Biology Open Software Suite. EMBOSS is a free Open Source software analysis package specially developed for the needs of the molecular biology (e.g. EMBnet) user community.
kallisto 0.43.1-IGB-gcc-4.9.4
0.44.0-IGB-gcc-4.9.4
kallisto is a program for quantifying abundances of transcripts from RNA-Seq data, or more generally of target sequences using high-throughput sequencing reads.
genometools 1.5.10-IGB-gcc-4.9.4 The GenomeTools genome analysis system is a free collection of bioinformatics tools (in the realm of genome informatics) combined into a single binary named gt. It is based on a C library named “libgenometools” which consists of several modules.
FLASH2 2.2.00-IGB-gcc-4.9.4 FLASH (Fast Length Adjustment of SHort reads) is an accurate and fast toolto merge paired-end reads that were generated from DNA fragments whoselengths are shorter than twice the length of reads. Merged read pairs resultin unpaired longer reads, which are generally more desired in genomeassembly and genome analysis processes.
Stacks 1.47-IGB-gcc-4.9.4 Stacks is a software pipeline for building loci from short-read sequences, such as those generated on the Illumina platform. Stacks was developed to work with restriction enzyme-based data, such as RAD-seq, for the purpose of building genetic maps and conducting population genomics and phylogeography.
Circlator 1.5.1-IGB-gcc-4.9.4-Python-3.6.1 A tool to circularize genome assemblies.
PCRE .8.40-IGB-gcc-4.9.4 The PCRE library is a set of functions that implement regular expression pattern matching using the same syntax and semantics as Perl 5. - Homepage: http://www.pcre.org/
MAPGD 0.4.26-IGB-gcc-4.9.4 MAPGD is a series of related programs that estimate allele frequency, heterozygosity, Hardy-Weinberg disequilibrium, linkage disequilibrium and identity-by-descent (IBD) coefficients from population genomic data using a statistically rigorous maximum likelihood approach.
GCC .4.9.4-2.28 The GNU Compiler Collection includes front ends for C, C++, Objective-C, Fortran, Java, and Ada, as well as libraries for these languages (libstdc++, libgcj,...). - Homepage: http://gcc.gnu.org/
pandoc 2.2.3.2 If you need to convert files from one markup format into another, pandoc is your swiss-army knife
SUNDIALS 2.6.2-IGB-gcc-4.9.4 SUNDIALS: SUite of Nonlinear and DIfferential/ALgebraic Equation Solvers
centrifuge 1.0.3-beta-IGB-gcc-4.9.4
1.0.4-beta-IGB-gcc-4.9.4
Centrifuge is a very rapid and memory-efficient system for the classification of DNA sequences from microbial samples, with better sensitivity than and comparable accuracy to other leading systems.
glproto .1.4.17-IGB-gcc-4.9.4 X protocol and ancillary headers
trf 4.0.9 Tandem Repeats Finder is a program to locate and display tandem repeats in DNA sequences.
gengetopt .2.22.6-IGB-gcc-4.9.4 Gengetopt is a tool to write command line option parsing code for C programs. - Homepage: https://www.gnu.org/software/gengetopt/gengetopt.html
minorseq 20180314-IGB-gcc-4.9.4 Minor Variant Calling and Phasing Tools
tensorly 0.4.2-IGB-gcc-4.9.4-Python-3.6.1 Simple and Fast Tensor Learning in Python
LINKS 1.8.5-IGB-gcc-4.9.4-Perl-5.24.1 LINKS is a scalable genomics application for scaffolding or re-scaffolding genome assembly drafts with long reads, such as those produced by Oxford Nanopore Technologies Ltd and Pacific Biosciences. It provides a generic alignment-free framework for scaffolding and can work on any sequences. It is versatile and supports not only long sequences as a source of long-range information, but also MPET pairs and linked-reads, such as those from the 10X Genomics GemCode and Chromium platform, via ARCS (http://www.bcgsc.ca/platform/bioinfo/software/arcs). Fill gaps in LINKS-derived scaffolds using Sealer (http://www.bcgsc.ca/platform/bioinfo/software/sealer).
ninja 1.8.2-IGB-gcc-4.9.4 Ninja is a small build system with a focus on speed. It differs from other build systems in two major respects: it is designed to have its input files generated by a higher-level build system, and it is designed to run builds as fast as possible.
Torch 20171018-IGB-gcc-4.9.4-Python-3.6.1 Torch is a scientific computing framework with wide support for machine learning algorithms that puts GPUs first. It is easy to use and efficient, thanks to an easy and fast scripting language, LuaJIT, and an underlying C/CUDA implementation.
TopHat 1.4.1
2.1.1-IGB-gcc-4.9.4
TopHat is a fast splice junction mapper for RNA-Seq reads. It aligns RNA-Seq reads to mammalian-sized genomes using the ultra high-throughput short read aligner Bowtie, and then analyzes the mapping results to identify splice junctions between exons.
icorn 0.97-IGB-gcc-4.9.4 Inputs: Reference Sequence (FASTA) & reads (FASTQ) & information of short reads
LMDB 0.9.22-IGB-gcc-4.9.4 LMDB is a fast, memory-efficient database. With memory-mapped files, it has the read performance of a pure in-memory database while retaining the persistence of standard disk-based databases.
DIYABC 2.1.0 a user-friendly approach to Approximate Bayesian Computation for inference on population history using molecular markers
primer3 2.4.0-IGB-gcc-4.9.4 Primer3 is a widely used program for designing PCR primers (PCR = "Polymerase Chain Reaction"). PCR is an essential and ubiquitous tool in genetics and molecular biology. Primer3 can also design hybridization probes and sequencing primers.
gffread ba7535f-IGB-gcc-4.9.4 The program gffread can be used to validate, filter, convert and perform various other operations on GFF files
RSeQC 2.6.4-IGB-gcc-4.9.4-Python-2.7.13 RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. Some basic modules quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while RNA-seq specific modules evaluate sequencing saturation, mapped reads distribution, coverage uniformity, strand specificity, transcript level RNA integrity etc.
SMARTdenovo 20170916-IGB-gcc-4.9.4-Perl-5.24.1 SMARTdenovo is a de novo assembler for PacBio and Oxford Nanopore (ONT) data. It produces an assembly from all-vs-all raw read alignments without an error correction stage. It also provides tools to generate accurate consensus sequences, though a platform dependent consensus polish tools (e.g. Quiver for PacBio or Nanopolish for ONT) are still required for higher accuracy.
Ragout 2.0-IGB-gcc-4.9.4 Ragout (Reference-Assisted Genome Ordering UTility) is a tool for chromosome assembly using multiple references.
Segway 2.0.1-IGB-gcc-4.9.4-Python-2.7.13 Segway is a tool for easy pattern discovery and identification in functional genomics data.
jupyterlab 0.34.10-IGB-gcc-4.9.4-Python-3.6.1 Project Jupyter exists to develop open-source software, open-standards, and services for interactive computing across dozens of programming languages.
PhiSpy 2.3-IGB-gcc-4.9.4-Python-2.7.13 A novel algorithm for finding prophages in microbial genomes that combines similarity-based and composition-based strategies
ncurses .5.9-IGB-gcc-4.9.4
.6.0
.6.0-IGB-gcc-4.9.4
The Ncurses (new curses) library is a free software emulation of curses in System V Release 4.0, and more. It uses Terminfo format, supports pads and color and multiple highlights and forms characters and function-key mapping, and has all the other SYSV-curses enhancements over BSD Curses.
jansson 2.6-IGB-gcc-4.9.4 Jansson is a C library for encoding, decoding and manipulating JSON data.
bazel 0.6.0-Java-1.8.0_121 Bazel is a build tool that builds code quickly and reliably. It is used to build the majority of Googles software.
ANTLR .2.7.7-IGB-gcc-4.9.4 ANTLR, ANother Tool for Language Recognition, (formerly PCCTS) is a language tool that provides a framework for constructing recognizers, compilers, and translators from grammatical descriptions containing Java, C#, C++, or Python actions.
SAMtools 0.1.20-IGB-gcc-4.9.4
1.4-IGB-gcc-4.9.4
1.4.1-IGB-gcc-4.9.4
1.5-IGB-gcc-4.9.4
1.7-IGB-gcc-4.9.4
SAM Tools provide various utilities for manipulating alignments in the SAM format, including sorting, merging, indexing and generating alignments in a per-position format.
VEP 92.4-IGB-gcc-4.9.4-Perl-5.24.1 VEP (Variant Effect Predictor) predicts the functional effects of genomic variants.
MUSCLE 3.8.31-IGB-gcc-4.9.4 MUSCLE is one of the best-performing multiple alignment programs according to published benchmark tests, with accuracy and speed that are consistently better than CLUSTALW. MUSCLE can align hundreds of sequences in seconds. Most users learn everything they need to know about MUSCLE in a few minutes—only a handful of command-line options are needed to perform common alignment tasks. - Homepage: http://drive5.com/muscle/
TransDecoder 5.1.0-IGB-gcc-4.9.4-Perl-5.24.1 TransDecoder identifies candidate coding regions within transcript sequences, such as those generated by de novo RNA-Seq transcript assembly using Trinity, or constructed based on RNA-Seq alignments to the genome using Tophat and Cufflinks.
PAML 4.9e-IGB-gcc-4.9.4 PAML is a package of programs for phylogenetic analyses of DNA or protein sequences using maximum likelihood. - Homepage: http://abacus.gene.ucl.ac.uk/software/paml.html
RNAmmer 1.2-IGB-gcc-4.9.4-Perl-5.24.1 Ribosomal RNA sub units
OCaml 4.05.0-IGB-gcc-4.9.4 OCaml is a general purpose industrial-strength programming language with an emphasis on expressiveness and safety. Developed for more than 20 years at Inria it benefits from one of the most advanced type systems and supports functional, imperative and object-oriented styles of programming.
Eigen .3.3.3-IGB-gcc-4.9.4 Eigen is a C++ template library for linear algebra: matrices, vectors, numerical solvers, and related algorithms. - Homepage: http://eigen.tuxfamily.org/index.php?title=Main_Page
Keras 2.0.6-IGB-gcc-4.9.4-Python-2.7.13
2.0.8-IGB-gcc-4.9.4-Python-3.6.1
2.1.2-IGB-gcc-4.9.4-Python-3.6.1
2.1.5-IGB-gcc-4.9.4-Python-3.6.1
2.2.0-IGB-gcc-4.9.4-Python-3.6.1
Keras is a high-level neural networks API, written in Python and capable of running on top of TensorFlow, CNTK, or Theano.
pygraphviz 1.3.1-IGB-gcc-4.9.4-Python-3.6.1 PyGraphviz is a Python interface to the Graphviz graph layout and visualization package. With PyGraphviz you can create, edit, read, write, and draw graphs using Python to access the Graphviz graph data structure and layout algorithms.
pomoxis 0.1.0-IGB-gcc-4.9.4-Python-3.6.1 Pomoxis contains a set of services to perform analysis of squiggles as they are produced in real-time along with fast pipelines for generating draft assemblies.
REAPR 1.0.18-IGB-gcc-4.9.4 REAPR is a tool that evaluates the accuracy of a genome assembly using mapped paired end reads, without the use of a reference genome for comparison. It can be used in any stage of an assembly pipeline to automatically break incorrect scaffolds and flag other errors in an assembly for manual inspection. It reports mis-assemblies and other warnings, and produces a new broken assembly based on the error calls. - Homepage: http://www.sanger.ac.uk/science/tools/reapr
BamTools 2.4.1-IGB-gcc-4.9.4 BamTools provides both a programmers API and an end-users toolkit for handling BAM files.
NetLogo 5.2.1
6.0.3
NetLogo is a multi-agent programmable modeling environment. It is used by many tens of thousands of students, teachers and researchers worldwide.
pssh 2.3.1-IGB-gcc-4.9.4-Python-2.7.13 PSSH provides parallel versions of OpenSSH and related tools, including pssh, pscp, prsync, pnuke and pslurp. This project includes psshlib which can be used within custom applications.
kyoto .20170410-IGB-gcc-4.9.4
20170410-IGB-gcc-4.9.4
Kyoto Tycoon is a lightweight network server on top of the Kyoto Cabinet key-value database, built for high-performance and concurrency. Some of its features include:
HiC-Pro 2.9.0-IGB-gcc-4.9.4-Python-2.7.13 HiC-Pro was designed to process Hi-C data, from raw fastq files (paired-end Illumina data) to the normalized contact maps. Since version 2.7.0, HiC-Pro supports the main Hi-C protocols, including digestion protocols as well as protocols that do not require restriction enzyme such as DNase Hi-C.
eigensoft 7.2.1-IGB-gcc-4.9.4 The EIGENSOFT package combines functionality from our population genetics methods (Patterson et al. 2006) and our EIGENSTRAT stratification correction method (Price et al. 2006).
treemix 1.13-IGB-gcc-4.9.4 TreeMix is a method for inferring the patterns of population splits and mixtures in the history of a set of populations. In the underlying model, the modern-day populations in a species are related to a common ancestor via a graph of ancestral populations. We use the allele frequencies in the modern populations to infer the structure of this graph.
BioPerl 1.7.1-IGB-gcc-4.9.4-Perl-5.24.1
1.7.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
Bioperl is the product of a community effort to produce Perl code which is useful in biology. Examples include Sequence objects, Alignment objects and database searching objects.
BWA 0.5.9-IGB-gcc-4.9.4
0.6.2-IGB-gcc-4.9.4
0.7.15-IGB-gcc-4.9.4
0.7.17-IGB-gcc-4.9.4
Burrows-Wheeler Aligner (BWA) is an efficient program that aligns relatively short nucleotide sequences against a long reference sequence such as the human genome. - Homepage: http://bio-bwa.sourceforge.net/
CheckM 1.0.7-IGB-gcc-4.9.4-Python-2.7.13 CheckM provides a set of tools for assessing the quality of genomes recovered from isolates, single cells, or metagenomes.
Rmpi 0.6-6-IGB-gcc-4.9.4-R-3.4.2 An interface (wrapper) to MPI APIs. It also provides interactive R manager and worker environment.
texlive 20170520-IGB-gcc-4.9.4 TeX Live is an easy way to get up and running with the TeX document production system. It provides a comprehensive TeX system with binaries for most flavors of Unix, including GNU/Linux, and also Windows. It includes all the major TeX-related programs, macro packages, and fonts that are free software, including support for many languages around the world.
biom-format 2.1.6-IGB-gcc-4.9.4-Python-2.7.13
2.1.6-IGB-gcc-4.9.4-Python-3.6.1
The BIOM file format (canonically pronounced biome) is designed to be a general-use format for representing biological sample by observation contingency tables.
graphviz 2.40.1-IGB-gcc-4.9.4
2.40.1-IGB-gcc-4.9.4-Python-2.7.13
Graphviz is open source graph visualization software. Graph visualization is a way of representing structural information as diagrams of abstract graphs and networks. It has important applications in networking, bioinformatics, software engineering, database and web design, machine learning, and in visual interfaces for other technical domains.
biodatabase 1.0-IGB-gcc-4.9.4 Scripts to create databases on the biodatabase machine.
IM-TORNADO 2.0.3.3-IGB-gcc-4.9.4-Python-2.7.13 A pipeline for 16S reads from paired-end libraries
tbl2asn 20180516 Tbl2asn is a command-line program that automates the creation of sequence records for submission to GenBank
file .5.30-IGB-gcc-4.9.4 The file command is a file type guesser, that is, a command-line tool that tells you in words what kind of data a file contains.
ant 1.10.1-Java-1.8.0_121 Apache Ant is a Java library and command-line tool whose mission is to drive processes described in build files as targets and extension points dependent upon each other. The main known usage of Ant is the build of Java applications. - Homepage: http://ant.apache.org/
squid 1.9g-IGB-gcc-4.9.4 A C library that is bundled with much of the above software. C function library for sequence analysis.
minimap 0.2-IGB-gcc-4.9.4
2.11-IGB-gcc-4.9.4
2.3-IGB-gcc-4.9.4
2.8-IGB-gcc-4.9.4
Minimap is an experimental tool to efficiently find multiple approximate mapping positions between two sets of long sequences, such as between reads and reference genomes, between genomes and between long noisy reads.
GMTK 1.4.4-IGB-gcc-4.9.4 The Graphical Models Toolkit (GMTK) is an open source, publicly available toolkit for rapidly prototyping statistical models using dynamic graphical models (DGMs) and dynamic Bayesian networks (DBNs). GMTK can be used for applications and research in speech and language processing, bioinformatics, activity recognition, and any time series application. GMTK has many features, including exact and approximate inference; a large variety of built-in factors including dense, sparse, and deterministic conditional probability tables, native support for ARPA backoff-based factors and factored language models, parameter sharing, gamma and beta distributions, dense and sparse Gaussian factors, heterogeneous mixtures, deep neural network factors, and time-inhomogeneous trellis factors; arbitrary order embedded Markov chains; a GUI-based graph viewer; flexible feature-file support and processing tools (supporting pfiles, HTK files, ASCII/binary, and HDF5 files); and both offline and streaming online inference methods that can be used for both parameter learning and prediction. More information is available in the documentation. All in all, GMTK offers a flexible, concise, and expressive probabilistic modeling framework with which one may rapidly specify a vast collection of temporal statistical models.
Python 2.7.13-IGB-gcc-4.9.4
3.6.1-IGB-gcc-4.9.4
Python is a programming language that lets you work more quickly and integrate your systems more effectively.
tRNAscan-SE 1.3.1-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded tRNAscan-SE: a tool for finding transfer RNAs
Biopython 1.68-IGB-gcc-4.9.4-Python-2.7.13
1.68-IGB-gcc-4.9.4-Python-3.6.1
Biopython is a set of freely available tools for biological computation writtenin Python by an international team of developers. It is a distributed collaborative effort todevelop Python libraries and applications which address the needs of current and future work inbioinformatics. - Homepage: http://www.biopython.org
PyCUDA 2017.1-IGB-gcc-4.9.4-Python-2.7.13 PyCUDA lets you access Nvidia‘s CUDA parallel computation API from Python. - Homepage: https://mathema.tician.de/software/pycuda/
libharu 2.3.0-IGB-gcc-4.9.4 libHaru is a free, cross platform, open source library for generating PDF files. - Homepage: http://libharu.org/
Sibelia 3.0.7-IGB-gcc-4.9.4 Sibelia is a tool for finding synteny blocks in closely related genomes, like different strains of the same bacterial species.
shortbred/diamond diamond/beta
diamond/devlocal
Anaconda3 5.0.1
5.1.0
Built to complement the rich, open source Python community,the Anaconda platform provides an enterprise-ready data analytics platform that empowers companies to adopt a modern open data science analytics architecture.
Lua 5.1.5-IGB-gcc-4.9.4
5.3.4-IGB-gcc-4.9.4
Lua is a powerful, fast, lightweight, embeddable scripting language. Lua combines simple procedural syntax with powerful data description constructs based on associative arrays and extensible semantics. Lua is dynamically typed, runs by interpreting bytecode for a register-based virtual machine, and has automatic memory management with incremental garbage collection, making it ideal for configuration, scripting, and rapid prototyping.
SNVer 0.5.3-Java-1.8.0_121 SNVer is a statistical tool for calling common and rare variants in analysis of pool or individual next-generation sequencing data. It reports one single overall p-value for evaluating the significance of a candidate locus being a variant, based on which multiplicity control can be obtained.
Ruby 2.4.2-IGB-gcc-4.9.4 Ruby is a dynamic, open source programming language with a focus on simplicity and productivity. It has an elegant syntax that is natural to read and easy to write.
structure 2.3.4-IGB-gcc-4.9.4 The program structure is a free software package for using multi-locus genotype data to investigate population structure.
MetaGeneAnnotator 20080819-x86-64 MetaGeneAnnotator is a gene-finding program for prokaryote and phage.
miniasm 0.2-IGB-gcc-4.9.4 Miniasm is a very fast OLC-based de novo assembler for noisy long reads. It takes all-vs-all read self-mappings (typically by minimap) as input and outputs an assembly graph in the GFA format. Different from mainstream assemblers, miniasm does not have a consensus step. It simply concatenates pieces of read sequences to generate the final unitig sequences. Thus the per-base error rate is similar to the raw input reads.
RDPClassifier 2.12-Java-1.8.0_152
2.2-Java-1.8.0_152
The RDP Classifier is a naive Bayesian classifier which was developed to provide rapid taxonomic placement based on rRNA sequence data. The RDP Classifier can rapidly and accurately classify bacterial and archaeal 16s rRNA sequences, and Fungal LSU sequences. It provides taxonomic assignments from domain to genus, with confidence estimates for each assignment.
454 2.8 The GS Data Analysis Software package includes the tools to investigate complex genomic variation in samples including de novo assembly, reference guided alignment and variant calling, and low abundance variant identification and quantification. - Homepage: http://454.com/products/analysis-software/index.asp
memprof 1.0 HPC Cluster Memory Profiling
qualimap 2.2.1-Java-1.8.0_121 Qualimap 2 is a platform-independent application written in Java and R that provides both a Graphical User Inteface (GUI) and a command-line interface to facilitate the quality control of alignment sequencing data and its derivatives like feature counts.
MAKER 2.31.9-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
3.00.0-beta-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
3.01.1-beta-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
MAKER is a portable and easily configurable genome annotation pipeline. Its purpose is to allow smaller eukaryotic and prokaryotic genome projects to independently annotate their genomes and to create genome databases. MAKER identifies repeats, aligns ESTs and proteins to a genome, produces ab-initio gene predictions and automatically synthesizes these data into gene annotations having evidence-based quality values. MAKER is also easily trainable: outputs of preliminary runs can be used to automatically retrain its gene prediction algorithm, producing higher quality gene-models on seusequent runs. MAKERs inputs are minimal and its ouputs can be directly loaded into a GMOD database. They can also be viewed in the Apollo genome browser; this feature of MAKER provides an easy means to annotate, view and edit individual contigs and BACs without the overhead of a database. MAKER should prove especially useful for emerging model organism projects with minimal bioinformatics expertise and computer resources.
magic 0.1-IGB-gcc-4.9.4-Python-3.6.1 A diffusion-based imputation method reveals gene-gene interactions in single-cell RNA-sequencing data
STAR 2.5.3a-IGB-gcc-4.9.4
2.6.0c-IGB-gcc-4.9.4
2.6.1b-IGB-gcc-4.9.4
STAR aligns RNA-seq reads to a reference genome using uncompressed suffix arrays.
NucleoATAC 0.3.4-IGB-gcc-4.9.4-Python-2.7.13 NucleoATAC is a python package for calling nucleosome positions and occupancy using ATAC-Seq data. Functions for calling nucleosomes are included in the nucleoatac command-line function. NucleoATAC also includes other utlities for working with ATAC-seq data under the pyatac function.
git-lfs 2.2.1-IGB-gcc-4.9.4 Git Large File Storage (LFS) replaces large files such as audio samples, videos, datasets, and graphics with text pointers inside Git, while storing the file contents on a remote server like GitHub.com or GitHub Enterprise.
h2o 3.14.0.3-IGB-gcc-4.9.4-R-3.3.3 R scripting functionality for H2O, the open source math engine for big data that computes parallel distributed machine learning algorithms such as generalized linear models, gradient boosting machines, random forests, and neural networks (deep learning) within various cluster environments.
gossamer 20170105-IGB-gcc-4.9.4 The gossamer bioinformatics suite contains goss, gossple, xenome, and electus
Supernova 1.1.5
1.2.0
1.2.1
2.0.0
2.0.1
2.1.0
2.1.1
Supernova is a software package for de novo assembly from Chromium Linked-Reads that are made from a single whole-genome library from an individual DNA source. A key feature of Supernova is that it creates diploid assemblies, thus separately representing maternal and paternal chromosomes over very long distances.
[(none) gompi] .4.9.4 GNU Compiler Collection (GCC) based compiler toolchain, including OpenMPI for MPI support. - Homepage: (none)
GCCcore .4.9.4
.7.3.0
The GNU Compiler Collection includes front ends for C, C++, Objective-C, Fortran, Java, and Ada, as well as libraries for these languages (libstdc++, libgcj,...). - Homepage: http://gcc.gnu.org/
plink 1.90 This is a comprehensive update to Shaun Purcells PLINK command-line program, developed by Christopher Chang with support from the NIH-NIDDKs Laboratory of Biological Modeling, the Purcell Lab at Mount Sinai School of Medicine, and others.
MPICH 3.0.4-GCC-4.9.4-2.28 MPICH v3.x is an open source high-performance MPI 3.0 implementation.It does not support InfiniBand (use MVAPICH2 with InfiniBand devices).
BS-Seeker 2.1.2-IGB-gcc-4.9.4-Python-2.7.13 BS Seeker 2 is a seamless and versatile pipeline for accurately and fast mapping the bisulfite-treated short reads. - Homepage: https://github.com/BSSeeker/BSseeker2
netCDF .4.4.1.1-IGB-gcc-4.9.4
4.4.1.1-IGB-gcc-4.9.4
NetCDF (network Common Data Form) is a set of software libraries and machine-independent data formats that support the creation, access, and sharing of array-oriented scientific data. - Homepage: http://www.unidata.ucar.edu/software/netcdf/
libxslt 1.1.29-IGB-gcc-4.9.4 Libxslt is the XSLT C library developed for the GNOME project (but usable outside of the Gnome platform).
cactus 20180705-IGB-gcc-4.9.4-Python-2.7.13 Cactus is a reference-free whole-genome multiple alignment program.
Salmon 0.11.3-IGB-gcc-4.9.4
0.8.2-IGB-gcc-4.9.4-Python-2.7.13
0.9.1-IGB-gcc-4.9.4
Salmon is a wicked-fast program to produce a highly-accurate, transcript-level quantification estimates from RNA-seq data.
LASTZ 1.04.00-IGB-gcc-4.9.4 LASTZ is a program for aligning DNA sequences, a pairwise aligner. Originally designed to handle sequences the size of human chromosomes and from different species, it is also useful for sequences produced by NGS sequencing technologies such as Roche 454. - Homepage: http://www.bx.psu.edu/~rsharris/lastz/
USEARCH 6.1.544
7.0.1090
9.2.64
USEARCH is a unique sequence analysis tool which offers search and clustering algorithms that are often orders of magnitude faster than BLAST.
MATLAB 2017a
2017b
MATLAB is a high-level language and interactive environment that enables you to perform computationally intensive tasks faster than with traditional programming languages such as C, C++, and Fortran.
graphtyper 1.3-IGB-gcc-4.9.4 Graphtyper is a highly scalable genotyping software. It represents a reference genome and known variants of a genomic region using an acyclic mathematical graph structure (a "pangenome reference"), which high-throughput sequence reads are re-aligned to for the purpose of discovering and genotyping SNPs and small indels.
ssaha2 2.5.5-IGB-gcc-4.9.4 SSAHA2 (Sequence Search and Alignment by Hashing Algorithm) is a pairwise sequence alignment program designed for the efficient mapping of sequencing reads onto genomic reference sequences.
snpomatic 1.0-IGB-gcc-4.9.4 SNP-o-matic is a fast, stringent short-read mapping software. It supports a multitude of output types and formats, for uses in filtering reads, alignments, sequence-based genotyping calls, assisted reassembly of contigs etc.
NWChem 6.6.revision27746-IGB-gcc-4.9.4-Python-2.7.13 NWChem aims to provide its users with computational chemistry tools that are scalable both in their ability to treat large scientific computational chemistry problems efficiently, and in their use of available parallel computing resources from high-performance parallel supercomputers to conventional workstation clusters. NWChem software can handle: biomolecules, nanostructures, and solid-state; from quantum to classical, and all combinations; Gaussian basis functions or plane-waves; scaling from one to thousands of processors; properties and relativity.
quast 4.6.1-IGB-gcc-4.9.4-Python-2.7.13
5.0.0-IGB-gcc-4.9.4-Python-3.6.1
QUAST performs fast and convenient quality evaluation and comparison of genome assemblies.
longranger 2.1.3
2.1.6
2.2.2
Long Ranger is a set of analysis pipelines that processes Chromium sequencing output to align reads and call and phase SNPs, indels, and structural variants. There are five main pipelines, each triggered by a longranger command
LibUUID 1.0.3-IGB-gcc-4.9.4 Portable uuid C library
QIIME 1.9.1 QIIME is an open-source bioinformatics pipeline for performing microbiome analysis from raw DNA sequencing data.
efignt beta
beta_private
devel
devlocal
prod
prod_private
BLAST 2.2.26-Linux_x86_64 Basic Local Alignment Search Tool, or BLAST, is an algorithm for comparing primary biological sequence information, such as the amino-acid sequences of different proteins or the nucleotides of DNA sequences.
SEPP 20180223-IGB-gcc-4.9.4-Python-2.7.13 SEPP stands for "SATe-enabled Phylogenetic Placement", and addresses the problem of phylogenetic placement of short reads into reference alignments and trees.
PyZMQ 16.0.2-IGB-gcc-4.9.4-Python-3.6.1 Python bindings for ZeroMQ
DIAMOND 0.8.38-IGB-gcc-4.9.4
0.9.10-IGB-gcc-4.9.4
0.9.16-IGB-gcc-4.9.4
0.9.9-IGB-gcc-4.9.4
Accelerated BLAST compatible local sequence aligner
Doxygen .1.8.13-IGB-gcc-4.9.4
1.8.13-IGB-gcc-4.9.4
Doxygen is a documentation system for C++, C, Java, Objective-C, Python, IDL (Corba and Microsoft flavors), Fortran, VHDL, PHP, C#, and to some extent D. - Homepage: http://www.doxygen.org
Assemblytics 3f570cd-IGB-gcc-4.9.4
df5361f-IGB-gcc-4.9.4
Analyze your assembly by comparing it to a reference genome
Porechop 0.2.3-IGB-gcc-4.9.4-Python-3.6.1 Porechop is a tool for finding and removing adapters from Oxford Nanopore reads.
bammds 20140602-IGB-gcc-4.9.4 Software that allows to create a multidimensional scaling (MDS) plot of populations for genetic data.
SQLite 3.17.0-IGB-gcc-4.9.4 SQLite: SQL Database Engine in a C Library
sambamba 0.6.6 sambamba view allows to efficiently filter SAM/BAM/CRAM files for alignments satisfying various conditions, as well as access its SAM header and information about reference sequences.
HarfBuzz .1.4.6-IGB-gcc-4.9.4 HarfBuzz is an OpenType text shaping engine. - Homepage: http://www.freedesktop.org/wiki/Software/HarfBuzz
Trinity 2.4.0-IGB-gcc-4.9.4
2.5.0-IGB-gcc-4.9.4
2.6.5-IGB-gcc-4.9.4
Trinity represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-Seq data. Trinity combines three independent software modules: Inchworm, Chrysalis, and Butterfly, applied sequentially to process large volumes of RNA-Seq reads. - Homepage: http://trinityrnaseq.github.io/
libpng .1.6.29-IGB-gcc-4.9.4 libpng is the official PNG reference library - Homepage: http://www.libpng.org/pub/png/libpng.html
perfsuite 1.1.4-IGB-gcc-4.9.4 PerfSuite is a collection of tools, utilities, and libraries for software performance analysis where the primary design goals are ease of use, comprehensibility, interoperability, and simplicity. This software can provide a good "entry point" for more detailed performance analysis and can help point the way towards selecting other tools and/or techniques using more specialized software if necessary (for example, tools/libraries from academic research groups or third-party commercial software).
GhostScript 9.21-IGB-gcc-4.9.4 Ghostscript is a versatile processor for PostScript data with the ability to render PostScript to different targets. It used to be part of the cups printing stack, but is no longer used for that. - Homepage: http://ghostscript.com
libreadline .6.3-IGB-gcc-4.9.4 The GNU Readline library provides a set of functions for use by applications that allow users to edit command lines as they are typed in. Both Emacs and vi editing modes are available. The Readline library includes additional functions to maintain a list of previously-entered command lines, to recall and perhaps reedit those lines, and perform csh-like history expansion on previous commands. - Homepage: http://cnswww.cns.cwru.edu/php/chet/readline/rltop.html
Circos 0.69-4-IGB-gcc-4.9.4-Perl-5.24.1 Circos is a software package for visualizing data and information. It visualizes data in a circular layout - this makes Circos ideal for exploring relationships between objects or positions. - Homepage: http://www.circos.ca/
GSL 2.3-IGB-gcc-4.9.4 The GNU Scientific Library (GSL) is a numerical library for C and C++ programmers. The library provides a wide range of mathematical routines such as random number generators, special functions and least-squares fitting. - Homepage: http://www.gnu.org/software/gsl/
udunits 2.2.26-IGB-gcc-4.9.4 UDUNITS supports conversion of unit specifications between formatted and binary forms, arithmetic manipulation of units, and conversion of values between compatible scales of measurement.
Pillow 5.1.0-IGB-gcc-4.9.4-Python-2.7.13
5.1.0-IGB-gcc-4.9.4-Python-3.6.1
Pillow is the friendly PIL fork by Alex Clark and Contributors. PIL is the Python Imaging Library by Fredrik Lundh and Contributors.
Tcl 8.6.6-IGB-gcc-4.9.4 Tcl (Tool Command Language) is a very powerful but easy to learn dynamic programming language,suitable for a very wide range of uses, including web and desktop applications, networking, administration,testing and many more. - Homepage: http://www.tcl.tk/
RepeatMasker 4.0.7-IGB-gcc-4.9.4-Perl-5.24.1
4.0.7-IGB-gcc-4.9.4-Perl-5.26.1-unthreaded
RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences.
IPython 5.3.0-IGB-gcc-4.9.4-Python-3.6.1 IPython provides a rich architecture for interactive computing with: Powerful interactive shells (terminal and Qt-based). A browser-based notebook with support for code, text, mathematical expressions, inline plots and other rich media. Support for interactive data visualization and use of GUI toolkits. Flexible, embeddable interpreters to load into your own projects. Easy to use, high performance tools for parallel computing.
libpthread-stubs .0.3-IGB-gcc-4.9.4 The X protocol C-language Binding (XCB) is a replacement for Xlib featuring a small footprint,latency hiding, direct access to the protocol, improved threading support, and extensibility.
tre 20161208-IGB-gcc-4.9.4 TRE is a lightweight, robust, and efficient POSIX compliant regexp matching library with some exciting features such as approximate (fuzzy) matching.The matching algorithm used in TRE uses linear worst-case time in the length of the text being searched, and quadratic worst-case time in the length of the used regular expression.In other words, the time complexity of the algorithm is O(M^2N), where M is the length of the regular expression and N is the length of the text. The used space is also quadratic on the length of the regex, but does not depend on the searched string. This quadratic behaviour occurs only on pathological cases which are probably very rare in practice.
gtest 1.8.0-IGB-gcc-4.9.4 Googles C++ test framework
GMAP-GSNAP 2017-11-15-IGB-gcc-4.9.4 GMAP: A Genomic Mapping and Alignment Program for mRNA and EST Sequences GSNAP: Genomic Short-read Nucleotide Alignment Program
MUMmer 3.23-IGB-gcc-4.9.4
4.0.0beta2-IGB-gcc-4.9.4
MUMmer is a system for rapidly aligning entire genomes, whether in complete or draft form. AMOS makes use of it.
picard 2.10.1-Java-1.8.0_121
2.10.1-Java-1.8.0_152
2.9.0-Java-1.8.0_121
2.9.4-Java-1.8.0_121
A set of tools (in Java) for working with next generation sequencing data in the BAM (http://samtools.github.io/hts-specs) format.
GDAL 2.3.1-IGB-gcc-4.9.4 GDAL is a translator library for raster geospatial data formats that is released under an X/MIT style Open Source license by the Open Source Geospatial Foundation. As a library, it presents a single abstract data model to the calling application for all supported formats. It also comes with a variety of useful commandline utilities for data translation and processing.
swift-t 1.3-IGB-gcc-4.9.4 Swift/T is a completely new implementation of the Swift language for high-performance computing. In this implementation, the Swift script is translated into an MPI program that uses the Turbine (hence, /T) and ADLB runtime libraries for highly scalable dataflow processing over MPI, without single-node bottlenecks.
FFmpeg 3.3-IGB-gcc-4.9.4 A complete, cross-platform solution to record, convert and stream audio and video. - Homepage: https://www.ffmpeg.org/
exonerate 2.2.0-IGB-gcc-4.9.4 Exonerate is a generic tool for pairwise sequence comparison. It allows you to align sequences using a many alignment models, either exhaustive dynamic programming or a variety of heuristics.
Trinotate 3.1.1-IGB-gcc-4.9.4-Perl-5.24.1 Trinotate is a comprehensive annotation suite designed for automatic functional annotation of transcriptomes, particularly de novo assembled transcriptomes, from model or non-model organisms. Trinotate makes use of a number of different well referenced methods for functional annotation including homology search to known sequence data (BLAST+/SwissProt), protein domain identification (HMMER/PFAM), protein signal peptide and transmembrane domain prediction (signalP/tmHMM), and leveraging various annotation databases (eggNOG/GO/Kegg databases). All functional annotation data derived from the analysis of transcripts is integrated into a SQLite database which allows fast efficient searching for terms with specific qualities related to a desired scientific hypothesis or a means to create a whole annotation report for a transcriptome.
clusterflow 0.5-IGB-gcc-4.9.4-Perl-5.25.1 Cluster Flow is workflow manager designed to run bioinformatics pipelines. It is operated through a single command cf, which can be used to launch, configure, monitor and cancel pipelines.
Prost 0.7.45-IGB-gcc-4.9.4-Python-2.7.13 Prost (PRocessing Of Small Transcripts) is a python application that quantifies and annotates microRNA (miRNA) expression in metazoans with assembled genomes. Prost works by counting short transcripts within a user-specifiable length range. These counted transcripts are aligned to a user specifiable genome allowing for post-transcriptional modification (e.g. untemplated additions, editing, alternative cutting) and then "binned" together based on genomic location. Each bin is then annotated with databases of mature miRNAs, hairpins, and other types of RNAs (the databases may be derived from miRBase, Ensembls BioMart, other databases, or may be custom built by the user).
MCL 14.137-IGB-gcc-4.9.4 The MCL algorithm is short for the Markov Cluster Algorithm, a fastand scalable unsupervised cluster algorithm for graphs (also known as networks) basedon simulation of (stochastic) flow in graphs. - Homepage: http://micans.org/mcl/
Boost .1.59.0-IGB-gcc-4.9.4
.1.63.0-IGB-gcc-4.9.4
.1.63.0-IGB-gcc-4.9.4-Python-2.7.13
Boost provides free peer-reviewed portable C++ source libraries. - Homepage: http://www.boost.org/
pilon 1.22-Java-1.8.0_121 Pilon is a software tool which can be used to:- Automatically improve draft assemblies- Find variation among strains, including large event detection
h5py .2.7.0-IGB-gcc-4.9.4-Python-2.7.13
2.7.0-IGB-gcc-4.9.4-Python-2.7.13
a toolkit for working with nanopore sequencing data from Oxford Nanopore. - Homepage: https://github.com/arq5x/poretools
bedops 2.4.30 BEDOPS is an open-source command-line toolkit that performs highly efficient and scalable Boolean and other set operations, statistical calculations, archiving, conversion and other management of genomic data of arbitrary scale.
byacc 20170709-IGB-gcc-4.9.4 Berkeley Yacc (byacc) is generally conceded to be the best yacc variant available.In contrast to bison, it is written to avoid dependencies upon a particular compiler.
RMBlast 2.6.0-IGB-gcc-4.9.4 RMBlast is a RepeatMasker compatible version of the standard NCBI blastn program. The primary difference between this distribution and the NCBI distribution is the addition of a new program "rmblastn" for use with RepeatMasker and RepeatModeler.
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