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Software | Version | Description |
---|---|---|
2.0.2-3 | de novo, parallel, sequence assembler for short reads | |
bamtools | 2.4.1+dfsg-2 | toolkit for manipulating BAM (genome alignment) files |
bedtools | 2.26.0+dfsg-5 | suite of utilities for comparing genomic features |
bioperl | 1.7.2-2 | Perl tools for computational molecular biology |
bioperl-run | 1.7.1-3 | BioPerl wrappers: scripts |
blast2 | 1:2.6.0-1 | Basic Local Alignment Search Tool |
bowtie | 1.2.2+dfsg-2 | Ultrafast memory-efficient short read aligner |
bowtie2 | 2.3.4.1-1 | Ultrafast memory-efficient short read aligner |
bwa | 0.7.17-1ubuntu0.1 | Burrows-Wheeler Aligner |
cd-hit | 4.6.8-1 | a suite of programs designed to quickly group sequences |
clustalw | 2.1+lgpl-5 | No description |
clustalx | 2.1+lgpl-6 | No description |
cufflinks | 2.2.1+dfsg.1-2 | Transcript assembly, differential expression and regulation for RNA-Seq |
diamond | 2.0.14 | sequence aligner for protein and translated DNA searches |
DiffBind | 3.0.15 | Compute differentially bound sites from multiple ChIP-seq experiments using affinity (quantitative) data |
ea-utils | 1.1.2+dfsg-4build1 | command-line tools for processing biological sequencing data |
emboss | 6.6.0+dfsg-6build1 | european molecular biology open software suite |
emboss-lib | 6.6.0+dfsg-6build1 | EMBOSS Libraries |
fastdnaml | 1.2.2-12 | Tool for construction of phylogenetic trees of DNA sequences |
fastqc | 0.11.5+dfsg-6 | A quality control application for high throughput sequence data |
fastx-toolkit | 0.0.14-5 | FASTQ/A short nucleotide reads pre-processing tools |
hmmer | 3.1b2+dfsg-5ubuntu1 | profile hidden Markov models for protein sequence analysis |
jaligner | 1.0+dfsg-4 | Smith-Waterman algorithm with Gotoh’s improvement |
jellyfish | 2.2.8-3build1 | count k-mers in DNA sequences |
khmer | 2.1.2+dfsg-3 | k0.7.17-1ubuntu0.1-mer counting, filtering and graph traversal |
libbiojava-java | 1:1.7.1-7 | Java API to biological data and applications (default version) |
libbiojava-java-demos | 1:1.7.1-7 | Example programs for BioJava |
macs | 2.1.1.20160309-2 | Model-based Analysis of ChIP-Seq on short reads sequencers |
mafft | 7.310-1 | Multiple alignment program for amino acid or nucleotide sequences |
maq | 0.7.1-7 | maps short fixed-length polymorphic DNA sequence reads to reference sequences |
med-bio | 3.0.1ubuntu1 | Debian Med bioinformatics packages |
med-cloud | 3.0.1ubuntu1 | Debian Med bioinformatics applications usable in cloud computing |
microbiomeutil | 20101212+dfsg1-1build1 | Microbiome Analysis Utilities |
minfi | 1.24.0 | Analyze Illumina Infinium DNA methylation arrays |
mothur | 1.39.5-2build1 | sequence analysis suite for research on microbiota |
mothur-mpi | 1.39.5-2build1 | mpi-enabled binary for mothur |
mrbayes-mpi | 3.2.6+dfsg-2 | Bayesian Inference of Phylogeny – mpi version |
mummer | 3.23+dfsg-3 | Efficient sequence alignment of full genomes |
muscle | 1:3.8.31+dfsg-3 | Multiple alignment program of protein sequences |
ncbi-blast+ | 2.6.0-1 | next generation suite of BLAST sequence search tools |
ncbi-blast+-legacy | 2.6.0-1 | NCBI Blast legacy call script |
ncbi-seg | 0.0.20000620-4 | tool to mask segments of low compositional complexity in amino acid sequences |
ncbi-tools-bin | 6.1.20170106-2 | NCBI libraries for biology applications (text-based utilities) |
ncbi-tools-x11 | 6.1.20170106-2 | NCBI libraries for biology applications (X-based utilities) |
paml | 4.9g+dfsg-3 | Phylogenetic Analysis by Maximum Likelihood (PAML) |
parafly | 0.0.2013.01.21-3build1 | parallel command processing using OpenMP |
phylip | 1:3.696+dfsg-5 | No description |
phyml | 3:3.3.20170530+dfsg-2 | Phylogenetic estimation using Maximum Likelihood |
picard-tools | 2.8.1+dfsg-3 | Command line tools to manipulate SAM and BAM files |
primer3 | 2.4.0-1ubuntu2 | Tool to design flanking oligo nucleotides for DNA amplification |
pymol | 1.8.4.0+dfsg-1build1 | Molecular Graphics System |
qiime | 3:3.3.20170530+dfsg-2 (1.8.0+dfsg-4ubuntu1)? | Quantitative Insights Into Microbial Ecology |
rasmol | 2.7.5.2-2 | Visualize biological macromolecules |
raxml | 8.2.11+dfsg-1 | Randomized Axelerated Maximum Likelihood of phylogenetic trees |
readseq | 1-12 | Conversion between sequence formats |
rsem | 1.2.31+dfsg-1 | RNA-Seq by Expectation-Maximization |
Rsubread | 2.4.3 | Mapping, quantification and variant analysis of sequencing data |
samtools | 1.7-1 | processing sequence alignments in SAM and BAM formats |
sift | 4.0.3b-6 | predicts if a substitution in a protein has a phenotypic effect |
sortmerna | 2.1-2 | tool for filtering, mapping and OTU-picking NGS reads |
stacks | 2.0Beta8c+dfsg-1 | pipeline for building loci from short-read sequences |
sumatra | 1.0.31-1 | fast and exact comparison and clustering of sequences |
swarm | 2.2.2+dfsg-1 | robust and fast clustering method for amplicon-based studies |
t-coffee | 2.2.2+dfsg-1 (11.00.8cbe486-6) | Multiple Sequence Alignment |
tophat | 2.1.1+dfsg1-1 | fast splice junction mapper for RNA-Seq reads |
transdecoder | 5.0.1-1 | find coding regions within transcripts |
trinityrnaseq | 2.5.1+dfsg-2 | RNA-Seq De novo Assembly |
trnascan-se | 1.3.1-1 | search for tRNA genes in genomic sequences |
velvet | 1.2.10+dfsg1-3build1 | Nucleic acid sequence assembler for very short reads |
velvet-example | 1.2.10+dfsg1-3build1 | Example data for the Velvet sequence assembler |
velvet-long | 1.2.10+dfsg1-3build1 | Nucleic acid sequence assembler for very short reads, long version |
velvetoptimiser | 2.2.6-1 | Automatically optimise Velvet do novo assembly parameters |
vsearch | 2.7.1-1 | tool for processing metagenomic sequences |
zsh | 5.4.2-3ubuntu3.1 | shell with lots of features |
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