Difference between revisions of "Biocluster Applications"
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− | |3.2.1 | + | |3.2.1(21), 3.3.0(21) |
− | | | + | |ERROR:102: Tcl command execution failed: set _description "A package of python scripts designed to analyze ultra-high-througphut sequencing data from the Illumina/Solexa platform for RNA-seq and ChIP-seq in metazoan genomes. The RNA-seq portion of ERANGE is described in our Nature Methods paper "Mapping and quantifying mammalian transcriptomes by RNA-Seq" (Mortazavi, 2008). ERANGE is built on top of Cistematic. " |
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|estscan | |estscan |
Revision as of 11:20, 25 February 2014
Application | Installed Versions | Description |
---|---|---|
454 | 2.6, 2.7, 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. |
AbundantOTU+ | 0.91b | AbundantOTU+ is the successor of AbundantOTU with additional functionality. AbundantOTU+ deals with sequences from rare species as well, compared to AbundantOTU!! |
abyss | 1.2.5, 1.3.3, 1.3.4 | 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. |
afni | 2011_12_21_2014 | AFNI (which might be an acronym for Analysis of Functional NeuroImages) is a set of C programs for processing, analyzing, and displaying functional MRI (FMRI) data - a technique for mapping human brain activity. It runs on Unix+X11+Motif systems, including SGI, Solaris, Linux, and Mac OS X. It is available free (in C source code format, and some precompiled binaries) for research purposes. |
allpathslg | 42911 | ALLPATHS-LG is our original short read assembler and it works on both small and large (mammalian size) genomes. To use it, you should first generate ~100 base Illumina reads from two libraries: one from ~180 bp fragments, and one from ~3000 bp fragments, both at about 45x coverage. Sequence from longer fragments will enable longer-range continuity. |
amos | 3.1.0 | The AMOS consortium is committed to the development of open-source whole genome assembly software. The project acronym (AMOS) represents our primary goal -- to produce A Modular, Open-Source whole genome assembler. |
AmpliconNoise | 1.2.7 | AmpliconNoise is a collection of programs for the removal of noise from 454 sequenced PCR amplicons. It involves two steps the removal of noise from the sequencing itself and the removal of PCR point errors. This project also includes the Perseus algorithm for chimera removal. |
art | 20110922 | ART is a set of simulation tools to generate synthetic next-generation sequencing reads. ART simulates sequencing reads by mimicking real sequencing process with empirical error models or quality profiles summarized from large recalibrated sequencing data. ART can also simulate reads using user own read error model or quality profiles. |
artemis | 14.0 | Artemis is a free genome browser and annotation tool that allows visualisation of sequence features, next generation data and the results of analyses within the context of the sequence, and also its six-frame translation. |
augustus | 2.6.1 | AUGUSTUS is a program that predicts genes in eukaryotic genomic sequences. |
b2g4pipe | 2.5 | adds environmental variables to blast2go pipe |
babraham | bioinformatics | Description of the module |
bali-phy | 2.1.1 | BAli-Phy is a Bayesian posterior sampler that employs Markov chain Monte Carlo to explore the joint space of alignment and phylogeny given molecular sequence data. Simultaneous estimation eliminates bias toward inaccurate alignment guide-trees, employs more sophisticated substitution models during alignment and automatically utilizes information in shared insertion/deletions to help infer phylogenies. |
bam2fastq | 1.1.0 | There are a growing number of general-purpose SAM/BAM manipulation programs, including SAMtools, Picard, and Bamtools. This tool is not intended to duplicate the complex suite of tasks those programs perform. Rather, it is simply intended to extract raw sequences (with qualities). We envision this tool being primarily useful to those wishing to duplicate or extend previous analyses. |
bamtools | 0.9.0, 2.3.0 | BamTools is a project that provides both a C++ API and a command-line toolkit for reading, writing, and manipulating BAM (genome alignment) files. |
bcbio-nextgen | 0.6.5 | A python toolkit providing best-practice pipelines for fully automated high throughput sequencing analysis. You write a high level configuration file specifying your inputs and analysis parameters. This input drives a parallel pipeline that handles distributed execution, idempotent processing restarts and safe transactional steps. The goal is to provide a shared community resource that handles the data processing component of sequencing analysis, providing researchers with more time to focus on the downstream biology. |
bedtools | 2.10.0, 2.10.1, 2.17.0 | Collectively, the bedtools utilities are a swiss-army knife of tools for a wide-range of genomics analysis tasks. The most widely-used tools enable genome arithmetic: that is, set theory on the genome. For example, bedtools allows one to intersect, merge, count, complement, and shuffle genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF. |
biodatabase | 1.0 | Scripts to create, delete, and manage mysql databases on IGB's biodatabase server |
biopieces | 0.48 | adds environmental variables, software, and bins to biopieces |
blast+ | 2.2.25+, 2.2.28+ | adds environmental variables to qiime and qiime |
blast-intel | 2.2.26 | The Basic Local Alignment Search Tool (BLAST) finds regions of local similarity between sequences. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance of matches. BLAST can be used to infer functional and evolutionary relationships between sequences as well as help identify members of gene families. |
blast | 2.2.26 | adds environmental variables to qiime and qiime |
blast2go | 2.5 | Description of the module |
blat | 0.34 | adds environmental variables to blat |
boost-intel | 1.54 | Boost provides free peer-reviewed portable C++ source libraries. |
boost | 1.54 | Boost provides free peer-reviewed portable C++ source libraries. |
bowtie | 0.12.8, 0.12.9, 1.0.0 | Bowtie is an ultrafast, memory-efficient short read aligner. It aligns short DNA sequences (reads) to the human genome at a rate of over 25 million 35-bp reads per hour. Bowtie indexes the genome with a Burrows-Wheeler index to keep its memory footprint small: typically about 2.2 GB for the human genome (2.9 GB for paired-end). |
bowtie2 | 2.0.0-beta6, 2.0.2, 2.0.5, 2.1.0 | adds environmental variables to Bowtie2 |
breseq | 0.24 | {Determine mutations in evolved microbes from next-generation sequencing data. |
bwa | 0.5.9, 0.7.5a | bio-bwa.sourceforge.net BWA is a software package for mapping low-divergent sequences against a large reference genome, such as the human genome |
cafe | 2.2, 3.0 | adds environmental variables to cafe |
casava | 1.8.2 | adds environmental variables to casava |
cd-hit | 4.6, 4.6.1 | CD-HIT is a very widely used program for clustering and comparing protein or nucleotide sequences. CD-HIT was originally developed by Dr. Weizhong Li at Dr. Adam Godzik's Lab at the Burnham Institute (now Sanford-Burnham Medical Research Institute) |
cdbfasta | 0.99 | fast indexing and retrieval of fasta records from flat file databases. |
chance | 1.0 | CHANCE - CHip-seq ANalytics and Confidence Estimation. songlab.ucsf.edu/Software.html |
chimera | 1.5.3, 1.6.2 | adds environmental variables for chimera |
cisgenome | 2.0 | An integrated tool for tiling array, ChIP-seq, genome and cis-regulatory element analysis. |
ClonalFrame | 1.2 | adds environmental variables to ClonalFrame |
clustalo | 1.2.0 | Clustal Omega is the latest addition to the Clustal family. It offers a significant increase in scalability over previous versions, allowing hundreds of thousands of sequences to be aligned in only a few hours. It will also make use of multiple processors, where present. In addition, the quality of alignments is superior to previous versions, as measured by a range of popular benchmarks. clustal.org/omega |
clustalw | 2.1 | adds environmental variables to clustalw |
cufflinks | 1.1.0, 1.3.0, 2.0.2, 2.1.1 | adds environmental variables to cufflinks |
cutadapt | 1.2 | cutadapt removes adapter sequences from high-throughput sequencing data. This is usually necessary when the read length of the sequencing machine is longer than the molecule that is sequenced, for example when sequencing microRNAs. |
cytoscape | 2.8.1, 2.8.3 | adds environmental variables to cytoscape |
EagleView | 2.2 | adds environmental variables to EagleView |
efiest | alpha, devel | adds environmental variables for EFI QUEST development branch |
EMBOSS | 6.5.7 | adds environmental variables to EMBOSS |
erange | 3.2.1(21), 3.3.0(21) | ERROR:102: Tcl command execution failed: set _description "A package of python scripts designed to analyze ultra-high-througphut sequencing data from the Illumina/Solexa platform for RNA-seq and ChIP-seq in metazoan genomes. The RNA-seq portion of ERANGE is described in our Nature Methods paper "Mapping and quantifying mammalian transcriptomes by RNA-Seq" (Mortazavi, 2008). ERANGE is built on top of Cistematic. " |
estscan | 3.0.3 | adds environmental variables to qiime and qiime |
fasta | 36.3.5d | adds environmental variables to qiime and qiime |
fasta_splitter | 1 | Description of the module |
fastqc | 0.10.1 | adds environmental variables to fastqc |
fastsimcoal2 | 1.1.1 | fast sequential Markov coalescent simulation of genomic data under complex evolutionary models. |
fasttree | 2.1.7 | 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. For large alignments, FastTree is 100-1,000 times faster than PhyML 3.0 or RAxML 7 |
fastx_toolkit | 0.0.13 | adds environmental variables to fastx_toolkit |
findpeaks | 3.1.9.2 | adds environmental variables to findpeaks |
freebayes | 0.9.6 | adds environmental variables to freebayes |
gatk | 1.6-5, 1.6-13, 2.5-2, 2.6-4 | 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. |
gcc | 4.8.1 | The GNU Compiler Collection includes front ends for C, C++, Objective-C, Fortran, Java, Ada, and Go, as well as libraries for these languages (libstdc++, libgcj,...). GCC was originally written as the compiler for the GNU operating system. The GNU system was developed to be 100% free software, free in the sense that it respects the user's freedom. |
geneid | 1.0 | adds environmental variables to geneid |
genomer | 0.0.10 | adds environmental variables to usearch |
genometools | 1.5.1 | 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. |
gff | 2.1 | Description of the module |
glimmer | 3.02 | adds environmental variables to bedtools |
gmap | 2011-09-14, 2013-03-31 | adds environmental variables to gmap and gsnap |
gmes | v2.3e | adds environmental variables to gmes |
gnuplot | 4.6.3 | Description of the module: Gnuplot is a portable command-line driven graphing utility for Linux, OS/2, MS Windows, OSX, VMS, and many other platforms |
graphviz | 2.32.0 | 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. |
gsl | 1.16 | The GNU Scientific Library (GSL) is a numerical library for C and C++ programmers. It is free software under the GNU General Public License. The library provides a wide range of mathematical routines such as random number generators, special functions and least-squares fitting. There are over 1000 functions in total with an extensive test suite. |
hmmer-mpi | 2.32-MPI-0.92 | adds environmental variables to hmmer-mpi |
hmmer | 2.3.2, 3.0 | 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). - |
htseq | 0.5.4 | HTSeq is a Python package that provides infrastructure to process data from high-throughput sequencing assays. |
icc | 2013.5.192 | Intel Studio XE 2013 |
idba-ud | 1.1.0 | adds environmental variables to idba-ud |
IGV | 2.1.24 | adds environmental variables to IGV |
IGVTools | 2.1.24 | adds environmental variables to qiime and qiime |
IMAGE | 2.33 | adds environmental variables to IMAGE |
ImageMagick | 6.7.8-9 | ImageMagick® is a software suite to create, edit, compose, or convert bitmap images. It can read and write images in a variety of formats (over 100) including DPX, EXR, GIF, JPEG, JPEG-2000, PDF, PhotoCD, PNG, Postscript, SVG, and TIFF. Use ImageMagick to resize, flip, mirror, rotate, distort, shear and transform images, adjust image colors, apply various special effects, or draw text, lines, polygons, ellipses and Bézier curves. |
infernal | 1.1rc1, 1.1rc2 | adds environmental variables to infernal 1.1 rc1 |
inparanoid | 4.1 | adds environmental variables for inparanoid |
iprscan | 4.8, 5.44, 5.45 | InterProScan is a bioinformatics tool that provides a one-stop-shop for automated sequence analysis of both protein and nucleic acid, the latter via a full six-frame translation. It offers the ability to identify both structural and functional regions of interest, based upon methods and models that have been generated by a large number of member groups ('member databases'). |
java | 1.6.0_41, 1.7.0_06-i386, 1.7.0_07 | adds environmental variables to java |
jellyfish | 1.1.6, 1.1.11 | JELLYFISH is a tool for fast, memory-efficient counting of k-mers in DNA. A k-mer is a substring of length k, and counting the occurrences of all such substrings is a central step in many analyses of DNA sequence. JELLYFISH can count k-mers using an order of magnitude less memory and an order of magnitude faster than other k-mer counting packages by using an efficient encoding of a hash table and by exploiting the 'compare-and-swap' CPU instruction to increase parallelism. |
khmer | 2013-05-06 | adds environmental variables khmer |
kmergenie | 1.5854 | Description of the module |
krona | 2.2 | adds environmental variables to qiime and qiime |
lamarc | 2.1.8 | adds environmental variables to cufflinks |
last | 278 | adds environmental variables to last |
lastz | 1.02.00 | adds environmental variables to lastz |
libstree | 0.4.2 | libstree is a generic suffix tree implementation, written in C. It can handle arbitrary data structures as elements of a string. Unlike most demo implementations, it is not limited to simple ASCII character strings. |
LR-TRIRLS | 20060531 | LR-TRIRLS stands for Logistic Regression with Truncated Regularized Iteratively Re-weighted Least Squares. This is our contribution to LR computation. |
lua | 5.1.4, 5.2.2 | adds environmental variables to lua |
MACS | 1.4.2, 2.0.10 | Next generation parallel sequencing technologies made chromatin immunoprecipitation followed by sequencing (ChIP-Seq) a popular strategy to study genome-wide protein-DNA interactions, while creating challenges for analysis algorithms. We present 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. |
mafft | 6.953 | adds environmental variables to mafft |
matlab-runtime | r2012b | http://www.mathworks.com/products/compiler/mcr/ The MATLAB Compiler Runtime (MCR) is a standalone set of shared libraries that enables the execution of compiled MATLAB applications or components on computers that do not have MATLAB installed |
matlab | 7.11.0.584 | adds environmental variables to matlab |
mcl | 12-068 | adds environmental variables to orthomcl |
MEGAN | 4.70.4, 5.1.0 | In metagenomics, the aim is to understand the composition and operation of complex microbial consortia in environmental samples through sequencing and analysis of their DNA. Similarly, metatranscriptomics and metaproteomics target the RNA and proteins obtained from such samples. |
meme | 4.9.0 | adds environmental variables to smrtanalysis-1.4.0 |
MetaGeneMark | 2010 | adds environmental variables to MetaGeneMark |
metAMOS | 1.2 | metAMOS is an integrated assembly and analysis pipeline for metagenomic data. It is built around the Bambus2 metagenomic scaffolder and includes many current tools for assembly, gene finding, and taxonomic classification. |
MetaVelvet | 1.2.02, 1.2.02-kmer245 | adds environmental variables to MetaVelvet |
mfinder | 1.2 | adds environmental variables to mfinder |
mira | 3.2.1 | adds environmental variables to mira |
MOCAT | 1.1 | adds environmental variables for MOCAT |
ModalClust | 0.2, 0.3 | adds environmental variables to ModalClust |
mothur | 1.8, 1.28.0, 1.31.2, 1.32.0, 1.32.1 | This project seeks to develop a single piece of open-source, expandable software to fill the bioinformatics needs of the microbial ecology community. We have incorporated the functionality of dotur, sons, treeclimber, s-libshuff, unifrac, and much more. In addition to improving the flexibility of these algorithms, we have added a number of other features including calculators and visualization tools. |
mpich | 3.0.4 | MPICH is a high performance and widely portable implementation of the Message Passing Interface (MPI) standard. |
mpich2 | 1.4.1p1, 1.5 | MPICH is a high performance and widely portable implementation of the Message Passing Interface (MPI) standard. |
msort | 1.0 | adds environmental variables to msort |
MUMmer | 3.23 | adds environmental variables to MUMmer |
muscle | 3.8.31 | adds environmental variables to velvet |
novocraft | 2.08, 2.08.02, 2.08.03, 3.00.01, 3.00.02, 3.00.05, 3.02 | adds environmental variables to novocraft |
oasas-kmer245 | 0.2.8 | Oases is a de novo transcriptome assembler designed to produce transcripts from short read sequencing technologies, such as Illumina, SOLiD, or 454 in the absence of any genomic assembly. |
oasas | 0.2.8 | Oases is a de novo transcriptome assembler designed to produce transcripts from short read sequencing technologies, such as Illumina, SOLiD, or 454 in the absence of any genomic assembly. |
OLB | 1.9.4 | adds environmental variables to qiime and qiime |
openmpi-intel | 1.6.3 | The Open MPI Project is an open source MPI-2 implementation that is developed and maintained by a consortium of academic, research, and industry partners. |
openmpi | 1.4.3, 1.6.3 | The Open MPI Project is an open source MPI-2 implementation that is developed and maintained by a consortium of academic, research, and industry partners. |
orthomcl | 2.0.2, 2.0.7 | adds environmental variables to orthomcl |
paml | 4.4 | adds environmental variables to paml |
parallel | 20121122 | adds environmental variables to orthomcl |
pathway-tools | 16.5 | adds environmental variables to pathway-tools |
PBJelly | 12.9.14 | adds environmental variables to PBJelly with smrtanalysis-1.4.0 |
peaksplitter | 1.0 | adds environmental variables to peaksplitter |
perfsuite | 1.0.0 | adds environmental variables to perfsuite |
perl | 5.16.1 | Perl 5 is a highly capable, feature-rich programming language with over 25 years of development. Perl 5 runs on over 100 platforms from portables to mainframes and is suitable for both rapid prototyping and large scale development projects. |
pfamscan | 1.0 | PFamscan |
phred | 0.020425.c | adds environmental variables to qiime and qiime |
phylip | 3.69 | adds environmental variables to phylip |
phymmbl | 4.0 | adds environmental variables to phymmbl |
picard-tools | 1.34, 1.73, 1.90 | adds environmental variables to picard-tools |
polyphen | 2.2.2 | PolyPhen-2 (Polymorphism Phenotyping v2) is a software tool which predicts possible impact of amino acid substitutions on the structure and function of human proteins using straightforward physical and evolutionary comparative considerations. |
pplacer | 1.0, 1.1 | adds environmental variables to pplacer |
prank | 121002 | adds environmental variables to prank |
prodigal | 2.0, 2.2 | adds environmental variables to prodigal |
python | 2.6.6, 2.7.3, 2.7.3-sqlite, 2.7.5-galaxy, 3.2.3 | adds environmental variables to Python 3.2 |
qiime | 1.3.0, 1.5.0, 1.6.0, 1.7.0, 1.8.0 | Loads qiimes environmental variables |
quake | 0.3.4 | Quake is a package to correct substitution sequencing errors in experiments with deep coverage (e.g. >15X), specifically intended for Illumina sequencing reads. |
quast | 2.2 | QUAST evaluates genome assemblies. It can works both with and without a given reference genome. The tool accepts multiple assemblies, thus is suitable for comparison. |
quest | alpha, devel | adds environmental variables for EFI QUEST development branch |
R | 2.15.0, 2.15.1, 2.15.2, 3.0.0, 3.0.2 | R is a language and environment for statistical computing and graphics. It is a GNU project which is similar to the S language and environment which was developed at Bell Laboratories (formerly AT&T, now Lucent Technologies) by John Chambers and colleagues. R can be considered as a different implementation of S. There are some important differences, but much code written for S runs unaltered under R. |
RAxML | 7.3.0 | RAxML (Randomized Axelerated Maximum Likelihood) is a program for sequential and parallel Maximum Likelihood based inference of large phylogenetic trees. It has originally been derived from fastDNAml which in turn was derived from Joe Felsentein’s dnaml which is part of the PHYLIP package. |
ray | 2.20, 2.30 | Ray -- Parallel genome assemblies for parallel DNA sequencing denovoassembler.sourceforge.net/index.html |
rdp_classifier | 2.5 | The RDP Classifier is a naive Bayesian classifier that can rapidly and accurately provides taxonomic assignments from domain to genus, with confidence estimates for each assignment. |
rdxplorer | 3.2 | adds environmental variables rdexplorer. use 'python rdxplorer.py to run' |
repeatmasker | 3.28 | RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences |
rockhopper | 1.2 | Description of the module Rockhopper, Rockhopper is a comprehensive and user-friendly system for computational analysis of bacterial RNA-seq data ttp://cs.wellesley.edu/~btjaden/Rockhopper/ |
rsa-tools | 2012-10-09 | adds environmental variables to qiime and qiime |
rstudio | 0.97.312 | adds environmental variables to R |
ruby | 1.9.3 | adds environmental variables to ruby |
samtools | 0.1.16, 0.1.18, 0.1.19 | SAM Tools provide various utilities for manipulating alignments in the SAM format, including sorting, merging, indexing and generating alignments in a per-position format. |
sam_comp | 0.7 | adds environmental variables Python 2.7.3 |
SICER | 1.1 | A clustering approach for identification of enriched domains from histone modification ChIP-Seq data |
signalp | 4.1 | adds environmental variables to perl |
smrtanalysis | 1.4.0, 2.0.1 | SMRT Analysis is a bioinformatics software suite for analyzing single molecule, real-time DNA sequencing data from Pacific Biosciences. This repository contains a link to download and view the SMRT Analysis source code. It is provided here for reference only and is currently not buildable. |
SnpEff | 3.2, 3.3e | Genetic variant annotation and effect prediction toolbox. It annotates and predicts the effects of variants on genes (such as amino acid changes). |
SOAP2 | 2.2 | adds environmental variables to SOAP2 |
SOAPdenovo-Trans | 1.02 | 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. |
SOAPdenovo | 2.04 | adds environmental variables to SOAPdenovo |
SOAPdenovo2 | r240 | adds environmental variables to SOAPdenovo2 |
SOAPec | 2.01, 2.02 | http://soap.genomics.org.cn/about.html |
SOAPErrorCorrection | 0.04 | adds environmental variables to SOAPErrorCorrection |
SOAPGapCloser | 1.12 | adds environmental variables to SOAPGapCloser |
SOAPprepare | 0.1 | adds environmental variables to SOAPdenovo |
speciateit | 184 | This is a beta version of a speciation pipeline for 16S rRNA amplicon data. In principle, the pipeline can be used for speciation based on any highly preserved gene. |
speciate_it | 184 | This is a beta version of a speciation pipeline for 16S rRNA amplicon data. In principle, the pipeline can be used for speciation based on any highly preserved gene. |
sratoolkit | 2.1.16 | adds environmental variables to sratoolkit |
srna-tools | 20130118 | adds environmental variables to srna-tools |
ssaha2 | 2.5.5 | 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. |
stacks | 0.9996, 0.99994 | adds environmental variables to stacks |
structure | 2.3.4 | The program structure is a free software package for using multi-locus genotype data to investigate population structure. Its uses include inferring the presence of distinct populations, assigning individuals to populations, studying hybrid zones, identifying migrants and admixed individuals, and estimating population allele frequencies in situations where many individuals are migrants or admixed. |
subread | 3.1.6(30) | ERROR:102: Tcl command execution failed: proc ModulesHelp { } { |
supfam | 1.75 | produce SCOP protein domain assignments using the SUPERFAMILY hidden Markov models (HMMs) and associated scripts. |
tabix | 0.2.6 | Tabix indexes a TAB-delimited genome position file in.tab.bgz and creates an index file in.tab.bgz.tbi when region is absent from the command-line. |
tcoffee | 10-r1613 | A collection of tools for Computing, Evaluating and Manipulating Multiple Alignments of DNA, RNA, Protein Sequences and Structures. |
tmhmm | 2.0 | adds environmental variables to tmhmm |
tophat | 1.4.1 | adds environmental variables to qiime and qiime |
tophat2 | 2.0.4, 2.0.5, 2.0.6, 2.0.7, 2.0.8, 2.0.10 | adds environmental variables to tophat 2 |
treemix | 1.12 | 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. |
trf | 4.04 | adds environmental variables to trf |
trimmomatic | 0.22, 0.27, 0.30 | adds environmental variables to trimmomatic |
trinityrnaseq-intel | r2013-02-25 | Trinity, developed at the Broad Institute and the Hebrew University of Jerusalem, represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-seq data. |
trinityrnaseq | r2012-06-08, r2013-02-25, r2013-08-14 | Trinity, developed at the Broad Institute and the Hebrew University of Jerusalem, represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-seq data. |
trinotate | trinotate_r20130826 | Description of the module |
truesight | 0.06 | TrueSight: Self-training Algorithm for Splice Junction Detection using RNA-seq. |
uchime | 4.2.40 | adds environmental variables to uchime |
usearch | 6.0.307, 6.1.544, 7.0.959 | USEARCH is a unique sequence analysis tool with thousands of users world-wide. USEARCH offers search and clustering algorithms that are often orders of magnitude faster than BLAST. |
USeq | 8.5.1 | adds environmental variables to USeq |
vcftools | 0.1.7, 0.1.11 | Welcome to VCFtools - a program package designed for working with VCF files, such as those generated by the 1000 Genomes Project. The aim of VCFtools is to provide methods for working with VCF files: validating, merging, comparing and calculate some basic population genetic statistics. |
velvet-kmer245 | 1.2.10 | 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. |
velvet | 1.1.04, 1.2.08, 1.2.10 | 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. |
VelvetOptimiser | 2.2.5 | VelvetOptimiser is a multi-threaded Perl script for automatically optimising the three primary parameter options (K, -exp_cov, -cov_cutoff) for the Velvet de novo sequence assembler. |
wessim | 1.0 | RAxML (Randomized Axelerated Maximum Likelihood) is a program for sequential and parallel Maximum Likelihood based inference of lar$ |
wgs | 7.0 | adds environmental variables to qiime and qiime |
wise | 2.2.3-rc7 | adds environmental variables to wise |