Skip to content

Commit

Permalink
Manifest configuration files for CloudBioLinux release 27 June 2012
Browse files Browse the repository at this point in the history
  • Loading branch information
chapmanb committed Jul 16, 2012
1 parent 4d25842 commit 16a3560
Show file tree
Hide file tree
Showing 4 changed files with 21,328 additions and 0 deletions.
296 changes: 296 additions & 0 deletions manifest/custom-packages.yaml
@@ -0,0 +1,296 @@
abyss:
description: Assembly By Short Sequences - a de novo, parallel, paired-end sequence
assembler.
homepage_uri: http://www.bcgsc.ca/platform/bioinfo/software/abyss
name: abyss
version: 1.3.3
beast:
description: 'BEAST: Bayesian MCMC analysis of molecular sequences.'
homepage_uri: http://beast.bio.ed.ac.uk/main_page
name: beast
version: ''
bedtools:
description: A flexible suite of utilities for comparing genomic features.
homepage_uri: https://code.google.com/p/bedtools/
name: bedtools
version: github
bfast:
description: 'BFAST: Blat-like Fast Accurate Search Tool.'
homepage_uri: http://sourceforge.net/apps/mediawiki/bfast/index.php?title=Main_Page
name: bfast
version: 0.7.0
bio4j:
description: Bio4j graph based database built on Neo4j with UniProt, GO, RefSeq
and more.
homepage_uri: http://www.bio4j.com/
name: bio4j
version: '0.7'
bowtie:
description: The bowtie short read aligner.
homepage_uri: http://bowtie-bio.sourceforge.net/index.shtml
name: bowtie
version: 0.12.7
bowtie2:
description: bowtie2 short read aligner, with gap support.
homepage_uri: http://bowtie-bio.sourceforge.net/bowtie2/index.shtml
name: bowtie2
version: 2.0.0-beta6
bwa:
description: 'BWA: aligns short nucleotide sequences against a long reference sequence.'
homepage_uri: http://bio-bwa.sourceforge.net/
name: bwa
version: 0.5.9
bx_python:
description: Tools for manipulating biological data, particularly multiple sequence
alignments
homepage_uri: https://bitbucket.org/james_taylor/bx-python/wiki/Home
name: bx_python
version: bitbucket
cljr:
description: Clojure package manager, cljr.
homepage_uri: http://github.com/liebke/cljr
name: cljr
version: ''
cloudman:
description: ' A meta method for installing all of CloudMan components.'
homepage_uri: ''
name: cloudman
version: ''
crisp:
description: Detect SNPs and short indels from pooled sequencing data.
homepage_uri: https://sites.google.com/site/vibansal/software/crisp/
name: crisp
version: '5'
cufflinks:
description: Cufflinks assembles transcripts, estimates their abundances, and tests
for differential expression and regulation in RNA-Seq samples.
homepage_uri: http://cufflinks.cbcb.umd.edu/
name: cufflinks
version: 2.0.0
dwgsim:
description: 'DWGSIM: simulating NGS data and evaluating mappings and variant calling.'
homepage_uri: http://sourceforge.net/apps/mediawiki/dnaa/index.php?title=Main_Page
name: dwgsim
version: 0.1.8
echo:
description: 'ECHO: A reference-free short-read error correction algorithm'
homepage_uri: http://uc-echo.sourceforge.net/
name: echo
version: '1_11'
emboss:
description: 'EMBOSS: A high-quality package of free, Open Source software for molecular
biology.'
homepage_uri: http://emboss.sourceforge.net/
name: emboss
version: 6.3.1
fastqc:
description: A quality control tool for high throughput sequence data.
homepage_uri: http://www.bioinformatics.babraham.ac.uk/projects/fastqc/
name: fastqc
version: 0.10.1
fastx_toolkit:
description: 'FASTX-Toolkit: collection of command line tools for Short-Reads FASTA/FASTQ
files preprocessing.'
homepage_uri: http://hannonlab.cshl.edu/fastx_toolkit/
name: fastx_toolkit
version: 0.0.13
freebayes:
description: Bayesian haplotype-based polymorphism discovery and genotyping.
homepage_uri: https://github.com/ekg/freebayes
name: freebayes
version: github
gatk:
description: 'GATK: library for writing efficient analysis tools using next-generation
sequencing data '
homepage_uri: http://www.broadinstitute.org/gsa/wiki/index.php/Home_Page
name: gatk
version: 1.6-11-g3b2fab9
gatk_queue:
description: Command-line scripting framework for defining multi-stage genomic analysis
pipelines.
homepage_uri: http://www.broadinstitute.org/gsa/wiki/index.php/GATK-Queue
name: gatk_queue
version: 1.6-11-g3b2fab9
gmap:
description: 'GMAP and GSNAP: A Genomic Mapping and Alignment Program for mRNA EST
and short reads.'
homepage_uri: http://research-pub.gene.com/gmap/
name: gmap
version: '2011-11-12'
hydra:
description: Hydra detects structural variation breakpoints in both unique and duplicated
genomic regions.
homepage_uri: https://code.google.com/p/hydra-sv/
name: hydra
version: 0.5.3
lastz:
description: LASTZ sequence alignment program.
homepage_uri: http://www.bx.psu.edu/miller_lab/dist/README.lastz-1.02.00/README.lastz-1.02.00a.html
name: lastz
version: 1.02.00
leinengin:
description: Clojure tool for project configuration and automation.
homepage_uri: http://github.com/technomancy/leiningen
name: leinengin
version: ''
macs:
description: Model-based Analysis for ChIP-Seq.
homepage_uri: http://liulab.dfci.harvard.edu/MACS/
name: macs
version: 1.4.2
matplotlib:
description: matplotlib is a python 2D plotting library which produces publication
quality figures
homepage_uri: http://matplotlib.sourceforge.net/
name: matplotlib
version: 1.0.1
mosaik:
description: 'MOSAIK: reference-guided aligner for next-generation sequencing technologies'
homepage_uri: http://code.google.com/p/mosaik-aligner/
name: mosaik
version: github
nginx:
description: Nginx open source web server.
homepage_uri: http://www.nginx.org/
name: nginx
version: 1.2.0
novoalign:
description: Novoalign short read aligner using Needleman-Wunsch algorithm with
affine gap penalties.
homepage_uri: http://www.novocraft.com/main/index.php
name: novoalign
version: V2.08.01
perm:
description: Efficient mapping of short sequences accomplished with periodic full
sensitive spaced seeds.
homepage_uri: https://code.google.com/p/perm/
name: perm
version: '3.6'
pgdspider:
description: PGDSpider format conversion for population genetics programs.
homepage_uri: http://www.cmpg.unibe.ch/software/PGDSpider/
name: pgdspider
version: 2.0.1.2
picard:
description: Command-line utilities that manipulate BAM files with a Java API.
homepage_uri: http://picard.sourceforge.net/
name: picard
version: '1.68'
plink_seq:
description: A toolset for working with human genetic variation data.
homepage_uri: http://atgu.mgh.harvard.edu/plinkseq/
name: plink_seq
version: '0.08'
proftpd:
description: Highly configurable GPL-licensed FTP server software.
homepage_uri: http://proftpd.org/
name: proftpd
version: 1.3.4a
pydoop:
description: pydoop; provides Hadoop access for Python.
homepage_uri: http://pydoop.sourceforge.net/docs/
name: pydoop
version: ''
rpy:
description: RPy is a very simple, yet robust, Python interface to the R Programming
Language.
homepage_uri: http://rpy.sourceforge.net/
name: rpy
version: 1.0.3
s3fs:
description: FUSE-based file system backed by Amazon S3.
homepage_uri: https://code.google.com/p/s3fs/
name: s3fs
version: '1.61'
samtools:
description: SAM Tools provide various utilities for manipulating alignments in
the SAM format.
homepage_uri: http://samtools.sourceforge.net/
name: samtools
version: 0.1.18
seal:
description: 'Install seal: process high-throughput sequencing with Hadoop.'
homepage_uri: http://biodoop-seal.sf.net/
name: seal
version: ''
sge:
description: Sun Grid Engine.
homepage_uri: ''
name: sge
version: ''
shrec:
description: Shrec is a bioinformatics tool for error correction of HTS read data.
homepage_uri: http://sourceforge.net/projects/shrec-ec/
name: shrec
version: '2.2'
snpeff:
description: Variant annotation and effect prediction tool.
homepage_uri: http://snpeff.sourceforge.net/
name: snpeff
version: '2_0_5'
solexaqa:
description: SolexaQA creates visual representations of data quality from FASTQ
files.
homepage_uri: http://solexaqa.sourceforge.net/
name: solexaqa
version: '1.4'
stacks:
description: 'Stacks: build loci out of a set of short-read sequenced samples.'
homepage_uri: http://creskolab.uoregon.edu/stacks/
name: stacks
version: '0.998'
stampy:
description: 'Stampy: mapping of short reads from illumina sequencing machines onto
a reference genome.'
homepage_uri: http://www.well.ox.ac.uk/project-stampy
name: stampy
version: 1.0.15
tassel:
description: 'TASSEL: evaluate traits associations, evolutionary patterns, and linkage
disequilibrium.'
homepage_uri: http://www.maizegenetics.net/index.php?option=com_content&task=view&id=89&Itemid=119
name: tassel
version: '3.0'
tophat:
description: TopHat is a fast splice junction mapper for RNA-Seq reads
homepage_uri: http://tophat.cbcb.umd.edu/
name: tophat
version: 2.0.0
tracer:
description: A program for analysing results from Bayesian MCMC programs such as
BEAST & MrBayes.
homepage_uri: http://beast.bio.ed.ac.uk/main_page
name: tracer
version: ''
transabyss:
description: Analyze ABySS multi-k-assembled shotgun transcriptome data.
homepage_uri: http://www.bcgsc.ca/platform/bioinfo/software/trans-abyss
name: transabyss
version: 1.3.2
trinity:
description: Efficient and robust de novo reconstruction of transcriptomes from
RNA-seq data.
homepage_uri: http://trinityrnaseq.sourceforge.net/
name: trinity
version: r2012-05-18
ucsc_tools:
description: Useful executables from UCSC.
homepage_uri: http://hgdownload.cse.ucsc.edu/admin/jksrc.zip
name: ucsc_tools
version: ''
varianttools:
description: Annotation, selection, and analysis of variants in the context of next-gen
sequencing analysis.
homepage_uri: http://varianttools.sourceforge.net/
name: varianttools
version: 1.0.1
vcftools:
description: Work with VCF files, such as those generated by the 1000 Genomes Project.
homepage_uri: http://vcftools.sourceforge.net/
name: vcftools
version: 0.1.7
velvet:
description: Sequence assembler for very short reads.
homepage_uri: http://www.ebi.ac.uk/~zerbino/velvet/
name: velvet
version: 1.2.05

0 comments on commit 16a3560

Please sign in to comment.