Software Repositories

In addition to the core software tools that are available by default, additional software is available via environment modules. For example, although Matlab is installed on the system, it is not available by default. Instead, we need to “load” its module first, e.g.

[alice@dev3 ~]$ module load matlab
[alice@dev3 ~]$ module list

Currently Loaded Modules:
  1) matlab/2020a

Then we can launch Matlab using:

[alice@dev3 ~]$ matlab -nosplash -nodesktop

To see what other “built-in” modules are available, use:

[alice@dev3 ~]$ module avail

In additional a set of built-in environment modules, there are also modules for software tools that are installed and maintained by other users or research groups. To access these, we first need to load the corresponding “Software Repository” module. For example, to get access to the repository and the software shared by the UCSF Computation Biology and Informatics core (CBI), make sure to load (“enable”) the repository first, e.g.

module load CBI

Then use module avail to list what modules and versions are available (or see below). Next, to actually get access to one or more of the shared software modules, use module load <name> or module load <name>/<version>. Here are a few examples:

module load bowtie2
module load bowtie2/2.2.6
module load r

It is possible to (i) enable a software repository and (ii) load a set of software tools in one call, e.g.

module load CBI r bwa bowtie2/2.2.6

Below are 3 software repositories, each providing a set of software tools.

Module Software Repository: built-in

Maintained by: Wynton Systems Administrators, Wynton
Enable repository: this software repository is always enabled
cuda
Versions: 7.5, 8.0, 9.1, 9.2, 10.1
julia
Versions: 0.6.4
matlab
Versions: 2018b, 2019a, 2019b, 2020a
matlab-runtime
Versions: 2020a
mpi
Versions: openmpi-x86_64

Module Software Repository: CBI

Maintained by: Henrik Bengtsson, Computational Biology and Informatics
Enable repository: module load CBI
asciigenome
ASCIIGenome: Text Only Genome Viewer
ASCIIGenome is a genome browser based on command line interface and designed for running from console terminals. Since ASCIIGenome does not require a graphical interface it is particularly useful for quickly visualizing genomic data on remote servers while offering flexibility similar to popular GUI viewers like IGV.
Example: ASCIIGenome --help.
URL: https://github.com/dariober/ASCIIGenome
Versions: 1.15.0
bamutil
bamUtil: Programs for Working on SAM/BAM Files
bamUtil is a repository that contains several programs that perform operations on SAM/BAM files. All of these programs are built into a single executable, bam.
Example: bam help.
URL: https://genome.sph.umich.edu/wiki/BamUtil, https://github.com/statgen/bamUtil
Versions: 1.0.14
bat
bat - A cat(1) Clone with Syntax Highlighting and Git Integration
A cat(1) clone with syntax highlighting and Git integration.
Example: bat README.md, bat scripts/*.sh, and bat src/*.c.
URL: https://github.com/sharkdp/bat
Warning: Only the most recent version of this software will be kept.
Versions: 0.13.0, 0.15.4
bcftools
BCFtools: Utilities for Variant Calling and Manipulating VCFs and BCFs
BCFtools is a set of utilities that manipulate variant calls in the Variant Call Format (VCF) and its binary counterpart BCF. All commands work transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed.
Example: bcftools --version
URL: http://www.htslib.org/
Versions: 1.9, 1.10, 1.10.2
bcl2fastq
bcl2fastq: Illumina Conversion Software
bcl2fastq Conversion Software both demultiplexes data and converts BCL files generated by Illumina sequencing systems to standard FASTQ file formats for downstream analysis.
Example: bcl2fastq --version
URL: https://support.illumina.com/sequencing/sequencing_software/bcl2fastq-conversion-software.html
Versions: 2.20.0
bedops
BEDOPS: The Fast, Highly Scalable and Easily-Parallelizable Genome Analysis Toolkit
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. Tasks can be easily split by chromosome for distributing whole-genome analyses across a computational cluster.
Example: bedops --version
URL: https://bedops.readthedocs.io/, https://github.com/bedops/bedops
Versions: 2.4.36, 2.4.37, 2.4.38, 2.4.39
bedtools2
bedtools2: The Swiss Army Knife for Genome Arithmetic
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.
Example: bedtools --version and ls $BEDTOOLS2_HOME/genomes/.
URL: https://github.com/arq5x/bedtools2/
Versions: 2.28.0, 2.29.1, 2.29.2
blast
BLAST+: Basic Local Alignment Search Tool
BLAST finds regions of similarity between biological sequences. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance.
Example: blastx -version
URL: https://blast.ncbi.nlm.nih.gov/Blast.cgi
Versions: 2.9.0, 2.10.1
blat
BLAT: Fast Sequence Search Command Line Tool
BLAT - client and server combined into a single program, first building the index, then using the index, and then exiting.
Example: blat
URL: https://genome.ucsc.edu/goldenPath/help/blatSpec.html
Versions: 36x4
bowtie
Bowtie: A Fast and Sensitive Gapped Read Aligner
Bowtie is an ultrafast, memory-efficient short read aligner.
Example: bowtie --version and ls $BOWTIE_HOME/{genomes,indexes}
Note: This is Bowtie v1 - not v2_.
URL: http://bowtie-bio.sourceforge.net/index.shtml
Versions: 1.2.3
bowtie2
Bowtie 2: A Fast and Sensitive Gapped Read Aligner
Bowtie 2 is an ultrafast and memory-efficient tool for aligning sequencing reads to long reference sequences.
Example: bowtie2 --version
URL: http://bowtie-bio.sourceforge.net/bowtie2/index.shtml
Versions: 2.3.5, 2.3.5.1, 2.4.1
bwa
BWA: Burrows-Wheeler Aligner
Burrows-Wheeler Aligner (BWA) is a software package for mapping low-divergent sequences against a large reference genome, such as the human genome.
Example: bwa.
URL: http://bio-bwa.sourceforge.net/
Versions: 0.7.17
byobu
byobu: Elegant Enhancement of the Otherwise Functional, Plain, Practical GNU Screen
Byobu is an elegant enhancement of the otherwise functional, plain, practical GNU Screen. Byobu includes an enhanced profile, configuration utilities, and system status notifications for the GNU screen window manager as well as the Tmux terminal multiplexer.
Example: byobu --version.
URL: http://byobu.org, https://github.com/dustinkirkland/byobu
Warning: Only the most recent version of this software will be kept.
Versions: 5.130, 5.133
CBI-testing
The Computational Biology and Informatics (CBI) Software Repository - TESTING ONLY!
This repository provides prototypical environment modules that can change at any time. They will live in this CBI-testing repository until they have proven to work and be stable - only then they will be considered for the main CBI repository. WARNING: Use at your own risk.
URL: http://cbi.ucsf.edu/
Versions:
cellranger
Cell Ranger: 10x Genomics Pipeline for Single-Cell Data Analysis
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.
Example: cellranger
URL: https://support.10xgenomics.com/single-cell-gene-expression/software/pipelines/latest/what-is-cell-ranger
Versions: 2.1.0, 3.0.2, 3.1.0
control-freec
Control FREEC: Control-FREE Copy Number and Genotype Caller
Prediction of copy numbers and allelic content using deep-sequencing data.
Example: freec.
URL: http://boevalab.com/FREEC/, https://github.com/BoevaLab/FREEC/
Versions: 11.5
cufflinks
Cufflinks: Transcriptome Assembly and Differential Expression Analysis for RNA-Seq
Cufflinks assembles transcripts, estimates their abundances, and tests for differential expression and regulation in RNA-Seq samples. It accepts aligned RNA-Seq reads and assembles the alignments into a parsimonious set of transcripts. Cufflinks then estimates the relative abundances of these transcripts based on how many reads support each one, taking into account biases in library preparation protocols.
Example: cufflinks.
URL: http://cole-trapnell-lab.github.io/cufflinks/, https://github.com/cole-trapnell-lab/cufflinks
Versions: 2.2.1
emacs
GNU Emacs: An Extensible, Customizable, Free/Libre Text Editor
At its core is an interpreter for Emacs Lisp, a dialect of the Lisp programming language with extensions to support text editing.
Example: emacs --version and emacs -nw.
URL: https://www.gnu.org/software/emacs/
Warning: Only the most recent version of this software will be kept.
Versions: 26.3
fastqc
FastQC: A Quality Control Analysis Tool for High Throughput Sequencing Data
FastQC is a program designed to spot potential problems in high througput sequencing datasets. It runs a set of analyses on one or more raw sequence files in fastq or bam format and produces a report which summarises the results.
Example: fastqc --version.
URL: https://www.bioinformatics.babraham.ac.uk/projects/download.html#fastqc, https://github.com/s-andrews/FastQC/
Versions: 0.11.8, 0.11.9
fzf
fzf - A Command-Line Fuzzy Finder
fzf is a general-purpose command-line fuzzy finder. It's an interactive Unix filter for command-line that can be used with any list; files, command history, processes, hostnames, bookmarks, git commits, etc.
Example: fzf --version and emacs "$(fzf)".
Note: To install tab completions and key bindinds to your shell, call $FZF_HOME/install. To uninstall, use $FZF_HOME/uninstall.
URL: https://github.com/junegunn/fzf, https://github.com/junegunn/fzf/wiki
Warning: Only the most recent version of this software will be kept.
Versions: 0.21.1
gatk
Genome Analysis Toolkit (GATK): Variant Discovery in High-Throughput Sequencing Data
Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size.
Example: gatk --help and gatk --list.
URL: https://software.broadinstitute.org/gatk/, https://github.com/broadinstitute/gatk/
Versions: 4.1.0.0, 4.1.2.0, 4.1.3.0, 4.1.4.0, 4.1.6.0, 4.1.7.0
gcta
GCTA: Genome-wide Complex Trait Analysis
A tool for Genome-wide Complex Trait Analysis (GCTA).
Example: gcta64.
URL: http://cnsgenomics.com/software/gcta/
Versions: 1.26.0, 1.92.3beta3, 1.92.4beta, 1.93.2beta
gdal
GDAL: Geospatial Data Abstraction Library
GDAL is an open source X/MIT licensed translator library for raster and vector geospatial data formats.
Example: gdalinfo --version
URL: https://gdal.org/, https://github.com/OSGeo/gdal
Versions: 2.4.3, 2.4.4
geos
GEOS: Geometry Engine, Open Source
GEOS (Geometry Engine - Open Source) is a C++ port of the JTS Topology Suite (JTS). It aims to contain the complete functionality of JTS in C++. This includes all the OpenGIS Simple Features for SQL spatial predicate functions and spatial operators, as well as specific JTS enhanced functions. GEOS provides spatial functionality to many other projects and products.
Example: geos-config --version.
URL: https://trac.osgeo.org/geos/
Versions: 3.5.2, 3.8.1
git-flow
git-flow: Git Extension Git Flow (AVH Edition)
A collection of Git extensions to provide high-level repository operations for Vincent Driessen's branching model.
Example: git flow.
URL: https://github.com/petervanderdoes/gitflow-avh, https://github.com/nvie/gitflow
Warning: Only the most recent version of this software will be kept.
Versions: 1.12.1, 1.12.3
gsl
GSL: Gnu Scientific Library
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.
Example: gsl-config --version
URL: https://www.gnu.org/software/gsl/
Versions: 2.6
hdf5
hdf5: A General Purpose Library and File Format for Storing Scientific Data
Hierarchical Data Format (HDF) is a set of file formats (HDF4, HDF5) designed to store and organize large amounts of data. The HDF5 format is designed to address some of the limitations of the HDF4 library, and to address current and anticipated requirements of modern systems and applications.
Example: h5cc --version
URL: https://www.hdfgroup.org/downloads/hdf5/
Versions: 1.10.6, 1.12.0
hisat2
HISAT2: Graph-based Alignment of Next Generation Sequencing Reads to a Population of Genomes
HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) to a population of human genomes (as well as to a single reference genome). Based on an extension of BWT for graphs [Sirén et al. 2014], we designed and implemented a graph FM index (GFM), an original approach and its first implementation to the best of our knowledge. In addition to using one global GFM index that represents a population of human genomes, HISAT2 uses a large set of small GFM indexes that collectively cover the whole genome (each index representing a genomic region of 56 Kbp, with 55,000 indexes needed to cover the human population). These small indexes (called local indexes), combined with several alignment strategies, enable rapid and accurate alignment of sequencing reads. This new indexing scheme is called a Hierarchical Graph FM index (HGFM).
Example: hisat2 --version.
URL: https://daehwankimlab.github.io/hisat2/, https://github.com/DaehwanKimLab/hisat2/
Versions: 2.1.0, 2.2.0
htop
htop - An Interactive Process Viewer for Unix
htop is an interactive process viewer for Unix systems. It is a text-mode application (for console or X terminals) and requires ncurses.
Example: htop.
URL: http://hisham.hm/htop/
Warning: Only the most recent version of this software will be kept.
Versions: 2.2.0
htslib
HTSlib: C Library for High-Throughput Sequencing Data Formats
HTSlib is an implementation of a unified C library for accessing common file formats, such as SAM, CRAM and VCF, used for high-throughput sequencing data, and is the core library used by samtools and bcftools. HTSlib also provides the bgzip, htsfile, and tabix utilities.
Example: bgzip --version, htsfile --version, and tabix --version.
URL: http://www.htslib.org/
Versions: 1.9, 1.10.2
igv
IGV: The Integrative Genomics Viewer
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. NOTE: IGV (>= 2.5.0) requires Java 11. Coincidentally, igvtools is integrated with IGV (>= 2.5.0).
Example: igv.
URL: https://software.broadinstitute.org/software/igv/
Versions: 2.7.0, 2.7.2, 2.8.2, 2.8.6, 2.4.19
igvtools
IGVTools: Tools for Pre-processing HT-Seq Data Files
The igvtools utility provides a set of tools for pre-processing data files. Note, igvtools moved to IGV as of IGV (>= 2.5.0).
Example: igvtools help.
URL: https://software.broadinstitute.org/software/igv/igvtools
Versions: 2.4.19
jags
JAGS: Just Another Gibbs Sampler
JAGS is Just Another Gibbs Sampler. It is a program for analysis of Bayesian hierarchical models using Markov Chain Monte Carlo (MCMC) simulation not wholly unlike BUGS.
Example: jags and man jags.
URL: http://mcmc-jags.sourceforge.net/
Versions: 4.3.0
kallisto
kallisto: Near-optimal RNA-Seq Quantification
kallisto is a program for quantifying abundances of transcripts from RNA-Seq data, or more generally of target sequences using high-throughput sequencing reads. It is based on the novel idea of pseudoalignment for rapidly determining the compatibility of reads with targets, without the need for alignment.
Example: kallisto version.
URL: https://pachterlab.github.io/kallisto/about.html, https://github.com/pachterlab/kallisto
Versions: 0.45.0, 0.45.1, 0.46.0, 0.46.1, 0.46.2
picard
Picard: Command-line tools for Manipulating High-throughput Sequencing Data and Formats
Picard is a set of command line tools for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
Example: picard -h, which is an alias for java -jar $PICARD_HOME/picard.jar -h
URL: http://broadinstitute.github.io/picard/, https://github.com/broadinstitute/picard
Versions: 2.21.1, 2.21.4, 2.22.2, 2.23.1
pindel
pindel: Detection of Indels and Structural Variations
Pindel can detect breakpoints of large deletions, medium sized insertions, inversions, tandem duplications and other structural variants at single-based resolution from next-gen sequence data. It uses a pattern growth approach to identify the breakpoints of these variants from paired-end short reads.
Example: pindel.
URL: https://www.sanger.ac.uk/science/tools/pindel, https://github.com/genome/pindel
Versions: 0.2.5b8
plink
PLINK: Whole Genome Association Analysis Toolset
PLINK is a free, open-source whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner. The focus of PLINK is purely on analysis of genotype/phenotype data, so there is no support for steps prior to this (e.g. study design and planning, generating genotype or CNV calls from raw data).
Example: plink --help.
URL: https://www.cog-genomics.org/plink/
Versions: 1.07, 1.90b6.10, 1.90b6.16, 1.90b6.18
plink2
PLINK2: Whole Genome Association Analysis Toolset
PLINK is a free, open-source whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner. The focus of PLINK is purely on analysis of genotype/phenotype data, so there is no support for steps prior to this (e.g. study design and planning, generating genotype or CNV calls from raw data).
Example: plink2 --help.
URL: https://www.cog-genomics.org/plink/2.0/, https://github.com/chrchang/plink-ng
Versions: 2.00a2LM, 2.00a2.3, 2.00a3LM
qtop
qtop: Monitor the State of Queueing Systems, Along with Related Information Relevant on HPC & Grid Clusters
qtop (pronounced queue-top) is a tool written in order to monitor the state of Queueing Systems, along with related information relevant on HPC & grid clusters. At present it supports PBS, SGE & OAR families. Please help to increase that list in the Python version of the tool, qtop.py!
Example: qtop and qtop -FGW.
URL: https://github.com/qtop/qtop
Warning: Only the most recent version of this software will be kept.
Versions: 0.9.20161222
r
R: The R Programming Language
The R programming language.
Example: R --version and Rscript --version.
URL: https://www.r-project.org/
Versions: 2.12.2, 2.13.0, 2.14.0, 2.15.0, 3.0.0, 3.1.0, 3.2.0, 3.3.0, 3.4.0, 3.5.0, 3.5.3, 3.6.0, 3.6.1, 3.6.2, 3.6.3, 4.0.0, 4.0.1, 4.0.2
r-siteconfig
R Site Configuration: Tweaks to R for the Current Compute Environment
Sets R options and environment variables customized for the current compute environment. Notably, it configures R to install packages from local CRAN and Bioconductor mirrors without the need for internet access.
Example: In R, install.packages("ggplot2").
Versions: 0.1
rclone
rclone: Rsync for Cloud Storage and More
Rclone is a command line program to sync files and directories to and from a large number of end points on the local file system, or remote file systems, and in the cloud.
Example: rclone --version, rclone --help, rclone config, and info rclone.
URL: https://rclone.org/, https://github.com/rclone/rclone
Warning: Only the most recent version of this software will be kept.
Versions: 1.51.0, 1.52.1
ripgrep
ripgrep - Recursively Searches Directories for a Regex Pattern
ripgrep is a line-oriented search tool that recursively searches your current directory for a regex pattern. By default, ripgrep will respect your .gitignore and automatically skip hidden files/directories and binary files. ripgrep is similar to other popular search tools like The Silver Searcher, ack and grep.
Example: rg --version and rg -i 'lorem ipsum'.
URL: https://github.com/BurntSushi/ripgrep
Warning: Only the most recent version of this software will be kept.
Versions: 11.0.2, 12.0.1, 12.1.1
samtools
SAMtools: Tools (written in C using htslib) for Manipulating Next-Generation Sequencing Data
SAMtools is a suite of programs for interacting with high-throughput sequencing data.
Example: samtools --version.
URL: http://www.htslib.org/
Versions: 1.9, 1.10
scl-devtoolset
SCL Developer Toolset: GNU Compiler Collection, GNU Debugger, etc.
Enables the CentOS Software Collection (SCL) devtoolset-8 in the current environment. This is an alternative to calling source scl_source enable devtoolset-8, which is an approach that is not officially supported by RedHat/CentOS.
Example: gcc --version.
URL: https://www.softwarecollections.org/en/scls/rhscl/devtoolset-8/
Versions: 4, 6, 7, 8
scl-python (part of CBI-testing)
SCL Python: Python with Additional Utilities via CentOS Software Collections [DEPRECATED]
Enables the CentOS Software Collection (SCL) rh-python36 in the current environment. This is an alternative to calling source scl_source enable rh-python36, which is not officially supported by RedHat/CentOS.
Example: python --version and pip --version.
URL: https://www.softwarecollections.org/en/scls/rhscl/rh-python36/
Warning: This module is DEPRECATED and should no longer be used because Python SCLs are deprecated, which in turn is because Python 3 is now available directly by CentOS.
Versions: 3.3, 3.4, 3.6
Note: To use this module, call module load CBI CBI-testing first.
shellcheck
ShellCheck: A Shell Script Static Analysis Tool
ShellCheck finds bugs in your shell scripts.
Example: shellcheck --version and shellcheck -x ~/.bashrc.
URL: https://www.shellcheck.net/, https://github.com/koalaman/shellcheck/
Warning: Only the most recent version of this software will be kept.
Versions: 0.6.0, 0.7.0, 0.7.1
snpeff
SnpEff: Genetic Variant Annotation and Effect Prediction Toolbox
SnpEff is a variant annotation and effect prediction tool. It annotates and predicts the effects of variants on genes (such as amino acid changes).
Example: snpEff -help, SnpSift -help, and ClinEff -help, which are aliases for java -jar $SNPEFF_HOME/snpEff/snpEff.jar -help, java -jar $SNPEFF_HOME/snpEff/SnpSift.jar -help, and java -jar $SNPEFF_HOME/clinEff/ClinEff.jar -help.
URL: http://snpeff.sourceforge.net/
Versions: 4.3t
sratoolkit
SRA Toolkit: Tools and Libraries for Using Data in the INSDC Sequence Read Archives
The SRA Toolkit and SDK from NCBI is a collection of tools and libraries for using data in the INSDC Sequence Read Archives.
Example: fastq-dump --help.
URL: https://ncbi.github.io/sra-tools/
Versions: 2.10.0, 2.10.4, 2.10.5, 2.10.7, 2.10.8
star
STAR: Spliced Transcripts Alignment to a Reference
STAR (Spliced Transcripts Alignment to a Reference) is a fast NGS read aligner for RNA-seq data.
Example: STAR --help.
URL: https://github.com/alexdobin/STAR
Versions: 2.7.0e, 2.7.0f, 2.7.1a, 2.7.2b, 2.7.3a, 2.7.5a
tmux
tmux: A Terminal Multiplexer
tmux is a terminal multiplexer. It lets you switch easily between several programs in one terminal, detach them (they keep running in the background) and reattach them to a different terminal. And do a lot more.
Example: tmux and man tmux.
URL: https://github.com/tmux/tmux/wiki
Warning: Only the most recent version of this software will be kept.
Versions: 2.8
tophat
TopHat: A Spliced Read Mapper for RNA-Seq
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.
Example: tophat --version.
URL: https://ccb.jhu.edu/software/tophat/index.shtml, https://github.com/infphilo/tophat
Versions: 2.1.1
tree
tree: List Content of Directories in a Tree-like Format
Tree is a recursive directory listing command that produces a depth indented listing of files, which is colorized ala dircolors if the LS_COLORS environment variable is set and output is to tty.
Example: tree --help.
URL: http://mama.indstate.edu/users/ice/tree/,
Warning: Only the most recent version of this software will be kept.
Versions: 1.8.0
varscan
VarScan: Variant Detection in Massively Parallel Sequencing Data
VarScan is a platform-independent mutation caller for targeted, exome, and whole-genome resequencing data generated on Illumina, SOLiD, Life/PGM, Roche/454, and similar instruments.
Example: varscan, which is an alias to java -jar $VARSCAN_HOME/VarScan.jar.
URL: https://dkoboldt.github.io/varscan/
Versions: 2.4.2
vcf-validator
vcf-validator: Validation Suite for Variant Call Format (VCF) Files
Validator for the Variant Call Format (VCF) implemented using C++11. It includes all the checks from the vcftools suite, and some more that involve lexical, syntactic and semantic analysis of the VCF input.
Example: vcf_validator --help, vcf-debugulator --help, and vcf-assembly-checker --help.
URL: https://github.com/EBIvariation/vcf-validator
Versions: 0.9.2, 0.9.3, 0.9.4
vcftools
VCFtools: Tools Written in Perl and C++ for Working with VCF Files
VCFtools is 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 easily accessible methods for working with complex genetic variation data in the form of VCF files.
Example: vcftools --version.
URL: https://vcftools.github.io/
Versions: 0.1.16
wynton-tools (part of CBI-testing)
Wynton Tools: Tools for the Wynton HPC Environment
A command-line tool for common Wynton HPC queries.
Example: wynton --help.
URL: https://github.com/UCSF-HPC/wynton-tools/
Versions: latest
Note: To use this module, call module load CBI CBI-testing first.

Module Software Repository: Sali

Maintained by: Ben Webb, Sali Lab Software Repository
Enable repository: module load Sali
allosmod
Versions:
amber
Versions: 11
anaconda
Versions:
blast
Versions: 2.2.26
blast+
Versions: 2.2.25, 2.2.28
boost
Versions: 1.68.0
cgal
Versions: 4.12.1
cmake
Versions: 3.12.2
concavity
Versions: 0.1
cryptosite
Versions:
cuda
Versions: 6.0.37, 7.5.18, 8.0.61, 9.0.176, 10.0.130
Cython
Versions: 0.25.2, 0.29.14
doxygen
Versions: 1.8.6, 1.8.15
dssp
Versions: 2.0.4, 2.2.1
eigen
Versions: 3.3.5
eman
Versions: 2.12, 2.2
featuresketch
Versions: 3.0
fpocket
Versions: 2.0
gcc
Versions: 5.1.1, 6.4.1, 7.3.1
ghostscript
Versions: 8.70
gnuplot
Versions: 5.0.5
hdf5
Versions: 1.8.14, 1.8.17, 1.10.1, 1.10.5
ImageMagick
Versions: 6.8.8.10
imp
Versions: last_ok_build-i386, last_ok_build-x86_64, last_ok_build, nightly-i386, nightly-x86_64, nightly, 2.0.0-i386, 2.0.0-x86_64, 2.0.0, 2.0.1-i386, 2.0.1-x86_64, 2.0.1, 2.1.0-i386, 2.1.0-x86_64, 2.1.0, 2.1.1-i386, 2.1.1-x86_64, 2.1.1, 2.2.0-i386, 2.2.0-x86_64, 2.2.0, 2.2.1-i386, 2.2.1-x86_64, 2.2.1, 2.3.0-i386, 2.3.0-x86_64, 2.3.0, 2.3.1-i386, 2.3.1-x86_64, 2.3.1, 2.4.0-i386, 2.4.0-x86_64, 2.4.0, 2.5.0-i386, 2.5.0-x86_64, 2.5.0, 2.6.0-i386, 2.6.0-x86_64, 2.6.0, 2.6.1-i386, 2.6.1-x86_64, 2.6.1, 2.6.2-i386, 2.6.2-x86_64, 2.6.2, 2.7.0-i386, 2.7.0-x86_64, 2.7.0, 2.8.0-i386, 2.8.0-x86_64, 2.8.0, 2.9.0-i386, 2.9.0-x86_64, 2.9.0, 2.10.0-i386, 2.10.0-x86_64, 2.10.0, 2.10.1-i386, 2.10.1-x86_64, 2.10.1, 2.11.0-i386, 2.11.0-x86_64, 2.11.0, 2.11.1-i386, 2.11.1-x86_64, 2.11.1, 2.12.0-i386, 2.12.0-x86_64, 2.12.0, 2.13.0-i386, 2.13.0-x86_64, 2.13.0
imp-fast
Versions: last_ok_build-i386, last_ok_build-x86_64, last_ok_build, nightly-i386, nightly-x86_64, nightly, 2.0.0-i386, 2.0.0-x86_64, 2.0.0, 2.0.1-i386, 2.0.1-x86_64, 2.0.1, 2.1.0-i386, 2.1.0-x86_64, 2.1.0, 2.1.1-i386, 2.1.1-x86_64, 2.1.1, 2.2.0-i386, 2.2.0-x86_64, 2.2.0, 2.2.1-i386, 2.2.1-x86_64, 2.2.1, 2.3.0-i386, 2.3.0-x86_64, 2.3.0, 2.3.1-i386, 2.3.1-x86_64, 2.3.1, 2.4.0-i386, 2.4.0-x86_64, 2.4.0, 2.5.0-i386, 2.5.0-x86_64, 2.5.0, 2.6.0-i386, 2.6.0-x86_64, 2.6.0, 2.6.1-i386, 2.6.1-x86_64, 2.6.1, 2.6.2-i386, 2.6.2-x86_64, 2.6.2, 2.7.0-i386, 2.7.0-x86_64, 2.7.0, 2.8.0-i386, 2.8.0-x86_64, 2.8.0, 2.9.0-i386, 2.9.0-x86_64, 2.9.0, 2.10.0-i386, 2.10.0-x86_64, 2.10.0, 2.10.1-i386, 2.10.1-x86_64, 2.10.1, 2.11.0-i386, 2.11.0-x86_64, 2.11.0, 2.11.1-i386, 2.11.1-x86_64, 2.11.1, 2.12.0-i386, 2.12.0-x86_64, 2.12.0, 2.13.0-i386, 2.13.0-x86_64, 2.13.0
libtau
Versions: 1.0.1
main
Versions: 2013
matlab
Versions: 9.5.0.944444
mist
Versions:
modeller
Versions: SVN-i386, SVN-x86_64, 9.10-i386, 9.10-x86_64, 9.10, 9.11-i386, 9.11-x86_64, 9.11, 9.12-i386, 9.12-x86_64, 9.12, 9.13-i386, 9.13-x86_64, 9.13, 9.14-i386, 9.14-x86_64, 9.14, 9.15-i386, 9.15-x86_64, 9.15, 9.16-i386, 9.16-x86_64, 9.16, 9.17-i386, 9.17-x86_64, 9.17, 9.18-i386, 9.18-x86_64, 9.18, 9.19-i386, 9.19-x86_64, 9.19, 9.20-i386, 9.20-x86_64, 9.20, 9.21-i386, 9.21-x86_64, 9.21, 9.22-i386, 9.22-x86_64, 9.22, 9.23-i386, 9.23-x86_64, 9.23, 9.24-i386, 9.24-x86_64, 9.24, SVN
modpipe
Versions: 2.0.1, 2.0.2, 2.1.0, 2.1.1, 2.1.2, 2.1.3, 2.2.0
muscle
Versions: 3.8.31
ninja
Versions: 1.6.0, 1.8.2
opencv
Versions: 3.4.3
openeye
Versions: 2012
patch_dock
Versions: 1.3
pcss
Versions:
phenix
Versions: 1.10.1.2155
profit
Versions: 3.1
psipred
Versions: 4.0
python2/biopython
Versions: 1.68, 1.69, 1.70
python2/bottleneck
Versions: 1.2.0, 1.2.1
python2/cycler
Versions: 0.10.0
python2/dateutil
Versions: 1.5, 2.6.1
python2/decorator
Versions: 4.0.11, 4.2.1
python2/functools32
Versions: 3.2.3
python2/h5py
Versions: 2.6.0, 2.7.0, 2.7.1
python2/ihm
Versions: 0.11
python2/lru_cache
Versions: 1.5
python2/matplotlib
Versions: 2.0.0, 2.0.2, 2.1.2
python2/mdp
Versions: 2.6
python2/msgpack
Versions: 0.5.6, 0.6.2
python2/networkx
Versions: 1.11
python2/nose
Versions: 1.3.7
python2/numexpr
Versions: 2.6.2, 2.6.4
python2/numpy
Versions: 1.12.0, 1.13.0, 1.14.1
python2/pandas
Versions: 0.19.2, 0.20.2, 0.22.0
python2/pkgconfig
Versions: 1.2.2
python2/protobuf
Versions: 2.3.0, 2.5.0
python2/pymc
Versions: 2.3.6
python2/pyparsing
Versions: 2.1.10
python2/pyrmsd
Versions: 4.1.git48ab119
python2/pytz
Versions: 2016.10
python2/scikit
Versions: 0.12, 0.18.1, 0.19.1
python2/scipy
Versions: 0.18.1, 0.19.0, 1.0.0
python2/six
Versions: 1.10.0
python2/tables
Versions: 3.3.0, 3.4.2, 3.5.2
python3/biopython
Versions: 1.75
python3/bottleneck
Versions: 1.3.1
python3/cycler
Versions: 0.10.0
python3/dateutil
Versions: 2.8.1
python3/decorator
Versions: 4.4.1
python3/h5py
Versions: 2.10.0
python3/ihm
Versions: 0.15
python3/joblib
Versions: 0.14.0
python3/kiwisolver
Versions: 1.1.0
python3/matplotlib
Versions: 3.1.2
python3/msgpack
Versions: 0.6.2
python3/networkx
Versions: 2.4
python3/nose
Versions: 1.3.7
python3/numexpr
Versions: 2.7.0
python3/numpy
Versions: 1.17.4
python3/pandas
Versions: 0.25.3
python3/pkgconfig
Versions: 1.5.1
python3/pyparsing
Versions: 2.4.5
python3/pyrmsd
Versions: 4.1.gita558b8a
python3/pytz
Versions: 2019.3
python3/scikit
Versions: 0.21.3
python3/scipy
Versions: 1.3.2
python3/six
Versions: 1.13.0
python3/tables
Versions: 3.6.1
relion
Versions: 1.4, 2.0.6, 3.0.git9a02562
rosetta
Versions: 3.5, 3.10
sali-libraries
Versions:
sali-libraries-i386
Versions:
sali-libraries-x86_64
Versions:
svm_light
Versions: 6.0.2
swig
Versions: 3.0.12
usearch
Versions: 4.0.43, 10.0.240
web_service
Versions:
zdock
Versions: 3.0.2

The above information was automatically generated on 2020-07-15 08:50:36 from querying module avail and module spider.