| aaindex |
Amino acid indices and similarity matrices |
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| abyss |
Assembly By Short Sequences - a de novo, parallel, paired-end sequence assembler |
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| amap |
Protein multiple-alignment-based sequence annealing |
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| augustus |
Eukaryotic gene predictor |
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| bamtools |
A programmer's API and an end-user's toolkit for handling BAM files |
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| bcftools |
Utilities for variant calling and manipulating VCF and BCF files |
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| bedtools |
Tools for manipulation and analysis of BED, GFF/GTF, VCF, SAM/BAM file formats |
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| bfast |
Blat-like Fast Accurate Search Tool |
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| biogrep |
Multithreaded tool for matching large sets of patterns against biosequence DBs |
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| biopandas |
Molecular Structures in Pandas DataFrames |
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| bioperl |
Perl tools for bioinformatics - Core modules |
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| bioperl-db |
Perl tools for bioinformatics - Perl API that accesses the BioSQL schema |
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| bioperl-network |
Perl tools for bioinformatics - Analysis of protein-protein interaction networks |
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| bioperl-run |
Perl wrapper modules for key bioinformatics applications |
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| biopython |
Python modules for computational molecular biology |
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| biosql |
A generic bioinformatics relational database model |
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| blat |
The BLAST-Like Alignment Tool, a fast genomic sequence aligner |
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| bowtie |
Popular short read aligner for Next-generation sequencing data |
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| bwa |
Burrows-Wheeler Alignment Tool, a fast short genomic sequence aligner |
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| cd-hit |
Clustering Database at High Identity with Tolerance |
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| clustal-omega |
Scalable multiple alignment of protein sequences |
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| clustalw |
General purpose multiple alignment program for DNA and proteins |
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| clustalw-mpi |
An MPI implemention of the ClustalW general purpose multiple alignment algorithm |
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| clustalx |
Graphical interface for the ClustalW multiple alignment program |
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| cutg |
Codon usage tables calculated from GenBank |
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| dialign2 |
Multiple sequence alignment |
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| dialign-tx |
Greedy and progressive approaches for segment-based multiple sequence alignment |
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| elph |
Estimated Locations of Pattern Hits - Motif finder program |
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| embassy |
A meta-package for installing all EMBASSY packages (EMBOSS add-ons) |
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| embassy-cbstools |
EMBOSS integrated version of Applications from the CBS group |
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| embassy-clustalomega |
EMBOSS integrated version of Clustal Omega - Multiple Sequence Alignment |
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| embassy-domainatrix |
EMBOSS integrated version of Protein domain analysis add-on package |
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| embassy-domalign |
EMBOSS integrated version of Protein domain alignment add-on package |
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| embassy-domsearch |
EMBOSS integrated version of Protein domain search add-on package |
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| embassy-emnu |
EMBOSS integrated version of Simple menu of EMBOSS applications |
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| embassy-esim4 |
EMBOSS integrated version of sim4 - Alignment of cDNA and genomic DNA |
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| embassy-hmmer |
EMBOSS integrated version of HMMER wrapper - sequence analysis with profile HMMs |
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| embassy-iprscan |
EMBOSS integrated version of InterProScan motif detection add-on package |
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| embassy-mse |
EMBOSS integrated version of MSE - Multiple Sequence Screen Editor |
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| embassy-phylipnew |
EMBOSS integrated version of The Phylogeny Inference Package |
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| embassy-signature |
EMBOSS integrated version of Protein signature add-on package |
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| embassy-structure |
EMBOSS integrated version of Protein structure add-on package |
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| embassy-topo |
EMBOSS integrated version of Transmembrane protein display |
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| embassy-vienna |
EMBOSS integrated version of Vienna RNA package - RNA folding |
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| emboss |
The European Molecular Biology Open Software Suite - A sequence analysis package |
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| eugene |
Prokaryotic and Eukaryotic gene predictor |
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| exonerate |
Generic tool for pairwise sequence comparison |
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| fasta |
FASTA is a DNA and Protein sequence alignment software package |
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| fasttree |
Fast inference of approximately-maximum-likelihood phylogenetic trees |
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| fastx_toolkit |
Tools for Short Read FASTA/FASTQ file processing |
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| finchtv |
Graphical viewer for chromatogram files |
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| foldingathome |
Folding@Home is a distributed computing project for protein folding |
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| glimmer |
An HMM-based microbial gene finding system from TIGR |
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| glimmerhmm |
A eukaryotic gene finding system from TIGR |
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| gmap |
A Genomic Mapping and Alignment Program for mRNA and EST Sequences |
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| hmmer |
Sequence analysis using profile hidden Markov models |
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| HTSeq |
Python support for SAM/BAM/Bowtie/FASTA/Q/GFF/GTF files |
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| iedera |
Subset seed design tool for DNA sequence alignment |
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| infernal |
Inference of RNA alignments |
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| iqpnni |
Important Quartet Puzzling and NNI Operation |
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| kalign |
Global and progressive multiple sequence alignment |
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| kallisto |
Near-optimal RNA-Seq quantification |
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| lagan |
The LAGAN suite of tools for whole-genome multiple alignment of genomic DNA |
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| libgtextutils |
Gordon Text utils Library |
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| mafft |
Multiple sequence alignments using a variety of algorithms |
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| maq |
Mapping and Assembly with Qualities, mapping NGS reads to reference genomes |
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| maqview |
GUI for sci-biology/maq, a short read mapping assembler |
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| mcl |
A Markov Cluster Algorithm implementation |
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| mosaik |
A reference-guided aligner for next-generation sequencing technologies |
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| mothur |
A suite of algorithms for ecological bioinformatics |
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| mrbayes |
Bayesian Inference of Phylogeny |
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| mummer |
A rapid whole genome aligner |
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| muscle |
Multiple sequence comparison by log-expectation |
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| newick-utils |
Tools for processing phylogenetic trees |
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| pals |
Pairwise Aligner for Long Sequences |
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| paml |
Phylogenetic Analysis by Maximum Likelihood |
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| phylip |
The PHYLogeny Inference Package |
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| phyml |
Estimation of large phylogenies by maximum likelihood |
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| piler |
Analysis of repetitive DNA found in genome sequences |
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| pilercr |
Analysis of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPRs) |
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| plink |
Whole genome association analysis toolset |
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| poa |
Fast multiple sequence alignments using partial-order graphs |
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| prank |
Probabilistic Alignment Kit |
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| primer3 |
Primer Design for PCR reactions |
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| prints |
A protein motif fingerprint database |
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| probcons |
Probabilistic Consistency-based Multiple Alignment of Amino Acid Sequences |
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| prodigal |
Prokaryotic Dynamic Programming Genefinding Algorithm |
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| profphd |
Secondary structure and solvent accessibility predictor |
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| prosite |
A protein families and domains database |
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| pysam |
Python interface for the SAM/BAM sequence alignment and mapping format |
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| qrna |
Prototype ncRNA genefinder |
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| raxml |
Sequential, Parallel & Distributed Inference of Large Phylogenetic Trees |
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| rebase |
A restriction enzyme database |
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| recon |
Automated de novo identification of repeat families from genomic sequences |
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| rnaview |
Generates 2D displays of RNA/DNA secondary structures with tertiary interactions |
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| samtools |
Utilities for analysing and manipulating the SAM/BAM alignment formats |
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| seaview |
A graphical multiple sequence alignment editor |
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| seqan |
C++ Sequence Analysis Library |
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| sibsim4 |
A rewrite and improvement upon sim4, a DNA-mRNA aligner |
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| sim4 |
A program to align cDNA and genomic DNA |
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| STAR |
STAR aligner: align RNA-seq reads to reference genome uncompressed suffix arrays |
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| stride |
Protein secondary structure assignment from atomic coordinates |
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| t-coffee |
A multiple sequence alignment package |
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| tree-puzzle |
Maximum likelihood analysis for nucleotide, amino acid, and two-state data |
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| treeviewx |
A phylogenetic tree viewer |
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| trf |
Tandem Repeats Finder |
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| trnascan-se |
tRNA detection in large-scale genome sequences |
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| uchime |
Fast, accurate chimera detection |
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| ucsc-genome-browser |
The UCSC genome browser suite, also known as Jim Kent's library and GoldenPath |
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| unafold |
Unified Nucleic Acid Folding and hybridization package |
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| update-blastdb |
update_blastdb.pl for local blast db maintainance |
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| vcftools |
Tools for working with VCF (Variant Call Format) files |
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| velvet |
A sequence assembler for very short reads |
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| wise |
Intelligent algorithms for DNA searches |
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| yass |
Genomic similarity search with multiple transition constrained spaced seeds |
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Packages