| description | de novo, parallel, paired-end sequence assembler that is designed for short reads |
| version | 1.2.6 |
| description | reorder entries an alignement (in fasta format) according a ref sequences file (in fasta format) |
| version | 20111202 |
| description | Allegro is a complete linkage analysis package. Its features include parametric and non-parametric LOD score calculations and various features intended for genetic mapping. |
| version | 2.0 |
| description | ALOHOMORA is a software tool designed to facilitate genome-wide linkage studies performed with high-density single nucleotide polymorphism (SNP) marker panels |
| version | 0.33 |
| description | AMOS is collection of tools and class interfaces for the assembly of DNA sequencing reads. |
| version | 2.0.8 |
| description | Affymetrix Power Tools (APT) are a set of cross-platform command line programs that implement algorithms for analyzing and working with Affymetrix GeneChip® arrays. |
| version | 1.12.0 |
| description | The ARB software is a graphically oriented package comprising various tools for sequence database handling and data analysis. |
| version | 5.1 |
| description | Artemis is a genome viewer and annotation tool that allows visualization of sequence features and the results of analyses within the context of the sequence, and its six-frame translation. |
| version | 11 |
| description | no description provided |
| version | 2011-12-14 |
| description | Bayesian Analysis in Molecular Biology and Evolution. |
| version | 4.01 |
| description | Calculate simple mapping statistics with Samtools flagstat and BAMStats |
| version | NA |
| description | Illumina BCL Converter software |
| version | 1.7.1 |
| description | bedtools: a flexible suite of utilities for comparing genomic features. |
| version | 2.12.0 |
| description | BIONJ is a distance based phylogeny reconstruction algorithm, which is well suited for distances estimated from DNA or protein sequences. |
| version |
| description | The Basic Local Alignment Search Tool (BLAST) finds regions of local similarity between sequences. |
| version | 2.2.21 |
| description | Taxonomy report from a blast report |
| version | 2.0 |
| description | Extract identifier of blast hits (from the summary) and make a list in USA format |
| version | 1.1 |
| description | Blast filtering with taxonomic hierarchy information, genomic criteria |
| version | 1.0 |
| description | Washington University BLAST (WU BLAST) is a powerful software package for gene and protein identification, using sensitive, selective and rapid similarity searches of protein and nucleotide sequence databases. |
| version | 2.0 (20060504) |
| description | Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. |
| version | 1.0 |
| description | Bowtie is an ultrafast, memory-efficient short read aligner. |
| version | 0.12.7 |
| description | BOXSHADE is a program for pretty-printing multiple alignment output. |
| version | 3.3.1 |
| description | Burrows-Wheeler Aligner BWA is a program for aligning sequencing reads against a large reference genome (e.g. human genome). It has two major components, one for read shorter than 150bp and the other for longer reads. |
| version | 0.5.9 |
| description | DNA sequence assembly program. |
| version |
| description | fast heuristic DNA motif digger based a on greedy approach accompanied by bootstrapping. ChIPMunk identifies the strong motif with the maximum Discrete Information Content in a set of DNA sequences |
| version | v3 |
| description | Small tools for sequencer trace data. |
| version | 0.99 |
| description | Cut dna region in frame |
| version | 0.2.2 |
| description | Circos is a software package for visualizing data and information. It visualizes data in a circular layout |
| version | 0.54-1 |
| description | ClonalFrame is a computer package for the inference of bacterial microevolution using multilocus sequence data |
| version | 1.2 |
| description | CLUSTAL-OMEGA is a general purpose multiple sequence alignment program for proteins. |
| version | 1.0.2 |
| description | ClustalW is a general purpose multiple alignment program for DNA or proteins. |
| version | 2.0.12 |
| description | ClustalX is a new windows interface for the ClustalW multiple sequence alignment program. |
| version | 2.0.12 |
| description | CodonW is a program designed to simplify the Multivariate analysis (correspondence analysis) of codon and amino acid usage. |
| version | 1.4.4 |
| description | ComAlign is a program, that given a number of sequences, generates a number of heuristic alignments and combines these best possible. |
| version |
| description | The program combat implements the method for combined DNA/protein alignment. |
| version | 1.0 |
| description | Concatanation of two fasta files with same identifier |
| version | 1.00 |
| description | Consed is a tool for viewing, editing, sequence assemblies created with phrap. |
| version | 19 |
| description | CONSEL calculates the p-value using several testing procedures; the bootstrap probability, the Kishino-Hasegawa test, the Shimodaira-Hasegawa test, and the weighted Shimodaira-Hasegawa test. In addition to these conventional tests, CONSEL calculates the p-value based on the approximately unbiased test using the multi-scale bootstrap technique. |
| version | v0.1k |
| description | The CONSENSUS programs are a collection of programs for determining and analyzing DNA and protein patterns describing functional elements. |
| version |
| description | Clustal Ouput Structural Analysis. |
| version |
| description | Tools for building simulated genetic datas |
| version | 0.33 |
| description | Cufflinks assembles transcripts, estimates their abundances, and tests for differential expression and regulation in RNA-Seq samples |
| version | 1.2.0 |
| description | removes adapter sequences from high-throughput sequencing data |
| version | 0.9.4 |
| description | Small collection of programs to manipulate databanks files. |
| version | 0.99a |
| description | Divide-and-Conquer Multiple Sequence Alignment (DCA) is a program for producing fast, high quality simultaneous multiple sequence alignments of amino acid, RNA, or DNA sequences. |
| version | 1.1 |
| description | DIALIGN is a software program for multiple alignment. |
| version | 2.2.1 |
| description | Gene3D provides structural annotation for proteins in the main sequence databases. |
| version | 3.0rc2 |
| description | A dot-matrix program with interactive greyscale rendering for genomic DNA and Protein sequence analysis. |
| version | 3.1 |
| description | Definition of secondary structure of proteins given a set of 3D coordinates. |
| version | 2000 |
| description | EAGLET (Efficient Analysis of Genetic Linkage: Testing and Estimation) is a fast, flexible, and powerful program for finding disesae-related genes in the human genome. |
| version | 1.3 |
| description | EagleView is an information-rich genome assembler viewer with data integration capability. |
| version | 1.83 |
| description | Compute synonymous sequences that maximize protein evolutionary landscape exploration. |
| version | 1.0 |
| description | EMBOSS is "The European Molecular Biology Open Software Suite", a free Open Source software analysis package specially developed for the needs of the molecular biology (e.g. EMBnet) user community. |
| version | 6.3.1 |
| description | concatenate several alignments from several files (one per file ) |
| version | 20111202 |
| description | Extracts translation(s) from a Genbank or Embl entry. |
| version |
| description | The FASTA package provides a modular set of sequence comparison programs. |
| version | 3.6 (x4) |
| description | parse a file with fasta sequences replace the identifier of a fasta sequences by a short identifier and generate a file with renamed fasta sequences and a file of mapping |
| version | 1.0 |
| description | fastDNAml is a program for estimating maximum likelihood phylogenetic trees from nucleotide sequences. |
| version | 1.2.2 |
| description | Genetic Analysis Software |
| version | 4.1P |
| description | A quality control tool for high throughput sequence data. |
| version | 0.94 |
| description | The FASTX-Toolkit is a collection of command line tools for Short-Reads FASTA/FASTQ files preprocessing. |
| version | 0.0.13 |
| description | Intelligent searching of the PRINTS motif database |
| version | 3.596 |
| description | FASTQ files utilities |
| version | 0.99 |
| description | ClustalW is a general purpose multiple alignment program for DNA or proteins. |
| version | 1.2.2 |
| description | software library that makes writing efficient analysis tools using next-generation sequencing data |
| version | 1.3.19 |
| description | Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. |
| version | 0.91b |
| description | GCG is an integrated package of over 150 programs that allows you to manipulate and analyze nucleic acid and protein sequences. |
| version | 11.0 |
| description | 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. |
| version | 1.3.0 |
| description | Identification of complete gene structures in genomic DNA. |
| version | 1.0 |
| description | This script validates a given GFF3 file |
| version | r16092 |
| description | Multipoint analysis of pedigree data including: non-parametric linkage analysis, LOD-score computation, information-content mapping, haplotype reconstruction |
| version | 1.3 |
| description | GigaBayes is a short-read SNP and short-INDEL discovery program. |
| version | beta |
| description | Genomic Mapping and Alignment Program for mRNA and EST Sequences, Genomic Short-read Nucleotide Alignment Program |
| version | 2011-11-27 |
| description | G-Mo.R-Se is a method aimed at using RNA-Seq short reads to build de novo gene models. |
| version | NA |
| description | Graphical Overview of Linkage Disequilibrium |
| version | 2001,11,8 |
| description | Golden is a small databanks entries retriever. |
| version | 1.1a |
| description | Sequence-based Prediction of Minimum Generation Times for Bacteria and Archaea |
| version | v1.05 |
| description | Clusters of binding sites. |
| version | 1.0 |
| description | HMMER is an implementation of profile HMM methods for sensitive database searches using multiple sequence alignments as queries. |
| version | 3.0 |
| description | an accurate and efficient algorithm for discovering canonical and non-canonical splice junctions in short read datasets |
| version | 0.9.5 |
| description | Prediction of transmembrane helices and topology of proteins. |
| version | 2.1 |
| description | html4blast is a simple Text to HTML blast results formatter |
| version | 1.6a |
| description | package that provides infrastructure to process data from high-throughput sequencing assays. |
| version | 2011-12-02 |
| description | Package for using multi-locus genotype data to investigate population structure. |
| version | 20070713 |
| description | Genomewide identification of cisregulatory motifs and modules underlying gene coregulation using statistics and phylogeny |
| version | 1.69.0440 |
| description | Inference of RNA secondary structure alignments "covariance models" (CMs) |
| version | 1.0.2 |
| description | Signature Recognition Search Against the Integrated Resource of Protein Domains and Functional Sites |
| version | 4.6 |
| description | infer isoform and gene expression levels from high-throughput transcriptome sequencing (RNA-Seq) data |
| version | 1.0.5 |
| description | JSpecies is an easy to use, biologist-centric software designed to measure the probability if two genomes belonging to the same species or not. |
| version | 1.2.1 |
| description | kisSnp compares two sets of NGS raw reads, detecting Single Nucleotide Polymorphism occurring between the two sets |
| version | 1.05 |
| description | open source data integration, processing analysis, and exploration platform |
| version | 2.5.0 |
| description | Ktreedist calculate the minimum branch length distance (or K tree score) from one phylogenetic tree to another. The K tree score provides a measure of the difference in both topology and branch lengths between two trees after scaling one of them to have a global divergence as similar as possible to the other tree. |
| version | 1 |
| description | software for finkage and Association Modeling in Pedigrees. LAMP uses a maximum likelihood model to extract information on genetic linkage and association from samples of unrelated individuals, sib pairs, trios and larger pedigrees |
| version | 0.0.9 |
| description | Manipulation Environment for Genetic Analyses. |
| version | 2.4.5 |
| description | LVB uses parsimony to reconstruct phylogeny from a nucleotide alignment, using a simulated annealing heuristic search. |
| version | 2.3 |
| description | MACH 1.0 is a Markov Chain based haplotyper. It can resolve long haplotypes or infer missing genotypes in samples of unrelated individuals. |
| version | 1.0.16 |
| description | Model-based Analysis of ChIP-Seq |
| version | 1.3.7.1 |
| description | Model-based Analysis of ChIP-Seq |
| version | 1.4.0rc2 |
| description | Multiple alignment program for amino acid or nucleotide sequences |
| version | 6.849 |
| description | Programs for genetic linkage analysis and mapping genes underlying complex traits. |
| version | 3 |
| description | MapNext provides four mainly analysis: (i) unspliced alignment and clustering of reads, (ii) spliced alignment of transcriptomic reads, (iii) SNP detection and calculation of SNP frequency from population sequences, and (iv) storage of result data into database to make it available for more flexible query and further analyses. |
| version | N-A |
| description | Maq is a software that builds mapping assemblies from short reads generated by the next-generation sequencing machines. |
| version | 0.7.1 |
| description | Maqview is graphical read alignment viewer |
| version | 0.2.5 |
| description | Mauve is a system for efficiently constructing multiple genome alignments in the presence of large-scale evolutionary events such as rearrangement and inversion |
| version | 2.3.1 |
| description | Cluster algorithm for graphs |
| version | 09-182 |
| description | Manipulation Environment for Genetic Analyses. |
| version | 4.5.1 |
| description | Melting computes, for a nucleic acid duplex, the enthalpy, the entropy and the melting temperature of the helix-coil transitions. |
| version | 4.2g |
| description | Motif-based sequence analysis tools |
| version | 4.5.0 |
| description | MERLIN uses sparse trees to represent gene flow in pedigrees. |
| version | 1.1.2 |
| description | RNA and DNA secondary structure prediction using nearest neighbor thermodynamic rules. |
| version | 3.2 |
| description | Identification of transcription factor binding sites in ChIP-Seq data |
| version | 1.0 |
| description | Computer Program Package for Molecular Phylogenetics. |
| version | 2.3b2 |
| description | a BASH script to improve ML tree search with PhyML 3.* |
| version | 1.14 |
| description | MOSAIK is a suite comprising of three modular programs: MosaikBuild, MosaikAligner, and MosaikAssembler. |
| version | beta2007 |
| description | Modular sofwate system for microbial ecology studies |
| version | 1.18 |
| description | MrBayes is a program for the Bayesian estimation of phylogeny. |
| version | 3.1.2 |
| description | mreps is a software for identifying serial repeats (usually called tandem repeats) in DNA sequences. |
| version | 2.5 |
| description | MSA is a program to do multiple sequence alignment under the sum-of-pairs criterion. |
| version | 2.1 |
| description | MSAPROBS is a new and practial protein multiple sequence alignmentalgorithm based on pair hidden markov model and partition functionposterrior probabilities. |
| version | 0.9.4 |
| description | MSPcrunch, a filtering tool for Blast matches. |
| version | 2.5 |
| description | This software will allow you to align simultaneously several biological sequences. |
| version | 5.4.1 |
| description | MUMmer is a system for rapidly aligning entire genomes, whether in complete or draft form |
| version | 3.22 |
| description | Multiple alignment software for protein and nucleotide sequences. |
| version | 3.8.31 |
| description | MView reformats the results of a sequence database search (BLAST, FASTA, etc) or a multiple alignment (MSF, PIR, CLUSTAL, etc) adding optional HTML markup to control colouring and web page layout. |
| version | 1.49 |
| description | Coiled-coils protein prediction |
| version | 2.2 |
| description | predicts the subcellular location of eukaryotic proteins. |
| version | 1.0 |
| description | predicts the subcellular location of eukaryotic proteins. |
| version | 1.0 |
| description | predicts the subcellular location of eukaryotic proteins. |
| version | 3.1 |
| description | Normalization by Expected Uniquely Mappble Area |
| version | 1.1.0 |
| description | The Newick Utilities are a suite of Unix shell tools for processing phylogenetic trees. Functions include re-rooting, extracting subtrees, trimming, pruning, condensing, drawing (ASCII graphics or SVG). |
| version | 1.6 |
| description | NJplot is a tree drawing program able to draw any phylogenetic tree expressed in the Newick phylogenetic tree format. |
| version | 20051109 |
| description | Nucleosome Positioning from Sequencing |
| version | 1.3.2 |
| description | Solexa Off-Line Basecaller Software |
| version | 1.6 |
| description | Genome-scale oligonucleotide design for microarrays. |
| version | 2.1.4 |
| description | A Python Package for Phylogenetics |
| version | 0.87.r132 |
| description | PALMapper, the fusion of the short read mapper GenomeMapper and the short read aligner QPALMA, is an easy-to-use and flexible tool to accurately and efficiently align both transcriptome reads (spliced and unspliced) from RNA-Seq experiments against a reference genome |
| version | 0.4-rc4 |
| description | PAML is a package of programs for phylogenetic analyses of DNA or protein sequences using maximum likelihood. |
| version | 4.4c |
| description | Software package for inference of evolutionary trees. |
| version | 4b10 |
| description | Tools for the statistical analysis of family-based association studies. |
| version | 3.5 |
| description | Calculate SOF: Sequences with Optimal Folding properties |
| version | 0.99 |
| description | Detecting marker typing incompatibilities in pedigree data |
| version | 1.1 |
| description | PEDSTATS is a tool for quick validation and summary of any pair of pedigree and data files. |
| version | 0.6.12 |
| description | CNV detection from Illumina whole-genome SNP genotyping arrays. It has been extended to handle candidate gene SNP arrays, to handle recent high-density arrays with non-polymorphic markers (so-called CN markers), and to handle Affymetrix genome-wide arrays. |
| version | 2009.08.27 |
| description | The pftools package contains programs for generalized profile applications. |
| version | 2.3 |
| description | Software for haplotype reconstruction, and recombination rate estimation from population data. |
| version | 2.1.1 |
| description | phrap is a program for assembling shotgun DNA sequence data. |
| version | 1.090518 |
| description | The phred software reads DNA sequencing trace files, calls bases, and assigns a quality value to each called base. |
| version | 071220.b |
| description | PHYLIP is a package of programs for inferring phylogenies. |
| version | 3.67 |
| description | PhyloBayes is a Bayesian Monte Carlo Markov Chain (MCMC) sampler for phylogenetic reconstruction using protein alignments. |
| version | 2.3c |
| description | PHYML - A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. |
| version | 3.0.1 |
| description | A program built to compute phylogenetic trees in cases where events of homologous recombination have affected an alignment. Based on original phyml (c) Stephane Guindon |
| version | 2.4.4 |
| description | command-line utilities that manipulate SAM files |
| version | 2011-12-14 |
| description | Pattern-Induced Multi-sequence Alignment program. Performs a multi-sequence alignment of a set of (presumably related) sequences using an extension of our covering pattern construction algorithm. |
| version | 1.40 |
| description | analysis of genotype/phenotype data |
| version | 1.07 |
| description | PLINK/SEQ is an open-source C/C++ library for working with human genetic variation data |
| version | 0.07 |
| description | PolyPhred is a program that compares fluorescence-based sequences across traces obtained from different individuals to identify heterozygous sites for single nucleotide substitutions. |
| version | 5.04 |
| description | Pattern discovery tool. |
| version | 2.1 |
| description | Protein secondary structure prediction software. |
| version | 2.1.2 |
| description | A Computer Program for Automatically Selecting PCR Primers |
| version | 0.5 |
| description | PCR primer design tool. |
| version | 2.2.3 |
| description | Primer design software (mostly derived from primer 0.5). |
| version |
| description | Search for Prosite patterns in protein sequences. |
| version | 0.02a |
| description | Joint Linkage and/or Linkage Disequilibrium Analysis |
| version | 1.0.6b |
| description | PSORT is a program for the prediction of protein localization sites in cells. |
| version | 981201 |
| description | Program for bacterial protein subcellular localization prediction. |
| version | 2.1.0 |
| description | TREE-PUZZLE is a computer program to reconstruct phylogenetic trees from molecular sequence data by maximum likelihood. |
| version | 5.2 |
| description | multiple genome comparison |
| version | 1.0.0 |
| description | Linkage Disequilibrium Analyses for Quantitative and Discrete Traits. |
| version | 2.6.1 |
| description | Software program for generating space-filling pictures of molecules from PDB files. |
| version | 2.1 |
| description | QuantiSNP identifies putative copy number alterations from Illumina Infinium I/II SNP genotyping data. |
| version | v2.3 beta |
| description | QuickTree is a program for the rapid reconstruction of phylogenies by the Neighbor-Joining method. |
| version | 1.1 |
| description | Report bootstrap values found with consensus program (after bootstrap analysis) on related tree found with phylogeny algorithm without bootstrap analysis. |
| version | 1.00 |
| description | RELPAIR is a program that infers the relationships of pairs of individuals based on genetic marker data, either within families or across an entire sample. |
| version | 2.0.1 |
| description | RepeatMasker is a program that screens DNA sequences for interspersed repeats and low complexity DNA sequences. |
| version | 3.1.5 |
| description | Perform ab initio method to detect multiple repeats in genomes |
| version | 1 |
| description | A method for fast database search for all k-nucleotide repeats |
| version |
| description | display statistics of large sequence files from next generation sequencing projects stored in SAM/BAM format. |
| version | 1.08 |
| description | SAM Tools provide various utilities for manipulating alignments in the SAM format, including sorting, merging, indexing and generating alignments in a per-position format. |
| version | 0.1.17 |
| description | Methods and algorithms for statistical analysis of protein sequences. |
| version |
| description | Genomewide identification of cisregulatory motifs and modules underlying gene coregulation using statistics and phylogeny |
| version | 1.0 |
| description | Search for patterns in DNA and protein sequences. |
| version | 97 |
| description | a method for transcriptome reconstruction that relies solely on RNA-Seq reads and an assembled genome |
| version | NA |
| description | SeaView is a graphical multiple sequence alignment editor. |
| version |
| description | SEG programs filter low complexity regions in sequences. |
| version |
| description | Seq-Gen is a program that will simulate the evolution of nucleotide or amino acid sequences along a phylogeny, using common models of the substitution process. |
| version | 1.3.2 |
| description | filter fasta sequences based on their size. |
| version | 0.1 |
| description | Split up query into smaller overlapping chunks |
| version |
| description | Short read mapping against a target genome |
| version | 2.1.1 |
| description | A clustering approach for identification of enriched domains from histone modification ChIP-Seq data |
| version | 1.1 |
| description | Multiple Prosite motifs searching. |
| version | 1.0 |
| description | predict signal peptides in proteins |
| version | 3.0 |
| description | A coalescent program for the simulation of complex recombination patterns over large genomic regions under various demographic models. |
| version | 2.1.2 |
| description | SimWalk2 is a statistical genetics computer application for haplotype, parametric linkage, non-parametric linkage (NPL), identity by descent (IBD) and mistyping analyses on any size of pedigree. |
| version | 2.91 |
| description | SMILE is a tool that infers motifs in a set of sequences, according to some criterias. |
| version | 1.47 |
| description | It's a variant effect predictor tool, it predicts the effect of genetic variations (SNPs, insertions, deletions and MNPs) |
| version | 1.9 |
| description | It's a variant effect predictor tool, it predicts the effect of genetic variations (SNPs, insertions, deletions and MNPs) |
| version | 1.9 |
| description | Program for estimating frequencies of haplotypes of large numbers of diallelic markers from unphased genotype data from unrelated subjects. |
| version | 1.3.1 |
| description | Genome-wide detection of polymorphisms at nucleotide resolution with a single DNA microarray. |
| version | 1.1 |
| description | SOLAR is a package for genetic variance components analysis, including linkage analysis, quantitative genetic analysis, and covariate screening. |
| version | 4.1.5 |
| description | de novo splice junction discovery and alignment too |
| version | 1.0.0 |
| description | Sequence/Alignment format checker. |
| version | 0.99a |
| description | Data analysis and statistical software. |
| version | 10.0.1 |
| description | Package for using multi-locus genotype data to investigate population structure. |
| version | 2.2.2 |
| description | tabix: Generic indexer for TAB-delimited genome position files bgzip: Block compression/decompression utility |
| version | 0.2.4 |
| description | tacg is a command-line program that performs many of the common routines in pattern matching in biological strings. |
| version | 4.1.0 |
| description | predicts the subcellular location of eukaryotic proteins. |
| version | 1.1 |
| description | taxonomy extraction |
| version | 0.99 |
| description | A program to estimate the rate of molecular evolution and time-scale of a phylogeny from dated sequences. |
| version | 1.2 |
| description | prediction of transmembrane helices in proteins. |
| version | 2.0C |
| description | TopHat is a fast splice junction mapper for RNA-Seq reads. |
| version | 1.2.0 |
| description | Transmembrane topology prediction. |
| version | 1.10 |
| description | Aligns and finds the phylogeny at the same time for a set of homologous proteins or DNA/RNA sequences. |
| version |
| description | tRNA detection in large-scale genome sequence. |
| version | 1.23 |
| description | T-Coffee is a multiple sequence alignment package. |
| version | 3.93 |
| description | RNA and DNA secondary structure prediction |
| version | 3.8 |
| description | VAAL is a polymorphism discovery algorithm for short reads |
| version | 1.6 |
| description | tool for identifying SNPs and indels in massively parallel sequencing of individual and pooled samples |
| version | 2.2.8 |
| description | A program package designed for working with VCF files |
| version | 0.1.5 |
| description | Sequence assembler for very short reads |
| version | 1.1.02 |
| description | RNA Secondary Structure Prediction and Comparison. |
| version | 1.8.4 |
| description | application designed to make the generation of sequence logos as easy and painless as possible |
| version | 2.8.2 |
| description | Weighted Neighbor Joining. |
| version | 1.2.1 |
| description | Versatile molecular modelling package that is specialized on working with proteins and the molecules in their environment like water, ligands, nucleic acids, etc. |
| version | 20080408 |
| description | Sequence assembler for very short reads |
| version | v 4 |
| description | Wise2 is a package focused on comparisons of bio polymers, commonly DNA sequence and protein sequence. |
| version | 2.2.0 |
| description | Software for exon trapping. |
| version |
| description | This software is able to extract putative cassette structures that fulfill the criteria established from analysis of previously known cassettes from integrons and superintegrons. |
| version | 3.03 |