software_bioinformatics

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Aplicaciones Científicas

Bioinformatics, Chemistry, Physics, etc

índice : A|B|C|D|E|F|G|H|I|J|K|L|M|N|O|P|Q|R|S|T|U|V|W|X|Y|Z



 **#** | \\
 **Aplicación** | \\
 **Versión** | \\
 **Descripción** |
A
aragorn1.2.38tRNA (and tmRNA) detection
arb6.0.6Phylogenetic analysis of rRNA and other biological sequences such as amino acids
ascp3.9.9
B
bowtie20.7.17software package for mapping low-divergent sequences against a large reference genome, such as the human genome
bwa2.4.1alineación de secuencias y el análisis de secuencias en bioinformática
blast+2.9.0Alineamiento de secuencias de tipo local, ya sea de ADN, ARN o de proteínas
blast+2.10.0(default)Alineamiento de secuencias de tipo local, ya sea de ADN, ARN o de proteínas
blast2.2.26Alineamiento de secuencias de tipo local, ya sea de ADN, ARN o de proteínas
bedtools2.29.2swiss-army knife of tools for a wide-range of genomics analysis tasks
bedops2.4.38highly scalable and easily-parallelizable genome analysis toolkit
beagle-lib3.1.2high-performance library that can perform the core calculations at the heart of most Bayesian and Maximum Likelihood phylogenetics
bcftools1.10.2set of utilities that manipulate variant calls
bbtools38.86suite of fast, multithreaded bioinformatics tools designed for analysis of DNA and RNA sequence data
barrnap0.9predicts the location of ribosomal RNA genes in genomes
bamtools2.5.1toolkit for handling BAM files.
C
cufflinks2.10finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads
circos2.2.1Transcriptome assembly and differential expression analysis for RNA-Seq.
cutadapt0.69-9for visualizing data and information. It visualizes data in a circular layout
checkm1.1.2set of tools for assessing the quality of genomes recovered from isolates, single cells, or metagenomes
cdhit4.8.1Takes a fasta format sequence database as input and produces a set of 'non-redundant' (nr)…
canu1.9Fork of the Celera Assembler designed for high-noise single-molecule sequencing
D
diamond0.9.35molecular and crystal structure visualization software
E
F
G
gromacs2019.4Modelamiento Molecular
H
hmmer2.3.2biosequence analysis using profile hidden Markov models .
hmmer3.1b1biosequence analysis using profile hidden Markov models .
hmmer3.1b2biosequence analysis using profile hidden Markov models .
hmmer3.2.1biosequence analysis using profile hidden Markov models .
I
J
K
L
M
N
Namd22019-11-27-multicoreModelamiento Molecular
P
Q
R
R3.6.1Analísis Estadistico
W
WRF3.9.1Mesoscale numerical weather prediction
WRF4.0Mesoscale numerical weather prediction
X

 **6** | \\
 netcdf/c| \\
 4.7.3| \\
 Network Common Data Form|

 **7** | \\
 netcdf/fortran| \\
 4.5.2| \\
 Network Common Data Form|

 **8** | \\
 quantum-espresso/schrodinger| \\
 6.4.1-2019-4| \\
 Modelamiento Molecular|

 **32** | \\
 eggnog-mapper| \\
 2.0.1| \\
 tool for functional annotation of large sets of sequences based on fast orthology assignments using precomputed clusters|

 **33** | \\
 EMBOSS| \\
 6.6.0| \\
 European Molecular Biology Open Software Suite|

 **34** | \\
 FastANI| \\
 1.3| \\
 Produces accurate ANI estimates and is faster than alignment (e.g., BLAST)- based approaches.|

 **35** | \\
 vcftools| \\
 0.1.17| \\
 package designed for working with VCF files|

 **36** | \\
 Unicycler| \\
 0.4.9b| \\
 assembly pipeline for bacterial genomes|

 **37** | \\
 tRNAscan-SE| \\
 2.0.5| \\
 searches for tRNA genes in genomic sequences|

 **38** | \\
 trinityrnaseq| \\
 2.11.0| \\
 Trinity RNA-Seq de novo transcriptome assembly|

 **39** | \\
 trf| \\
 4.09| \\
 Analyze DNA sequences|

 **40** | \\
 TransDecoder| \\
 5.5.0| \\
 Assist in the identification of potential coding regions within ….|

 **41** | \\
 tophat| \\
 2.1.1| \\
 Alineación del rendimiento de las lecturas de secuenciación de cDNA …|

 **42** | \\
 tbl2asn| \\
 3.10.0| \\
 Automates the creation of sequence records for submission to GenBank|

 **43** | \\
 ssu-align| \\
 0.1.1| \\
 identifying, aligning, masking and visualizing archaeal 16S, bacterial 16S and eukaryotic 18S…|

 **44** | \\
 sratoolkit| \\
 2.10.7| \\
 Using the SRA Toolkit to convert .sra files into other formats …|

 **45** | \\
 SPAdes| \\
 3.14.1| \\
 Assembly toolkit containing various assembly pipelines.|

 **46** | \\
 SPAdes| \\
 3.13.2| \\
 Assembly toolkit containing various assembly pipelines.|

 **47** | \\
 SINA| \\
 1.6.1| \\
 accurate high-throughput multiple sequence alignment of ribosomal RNA genes.|

 **48** | \\
 seqtk| \\
 1.3| \\
 A fast and lightweight tool for processing sequences in the FASTA or FASTQ format.|

 **49** | \\
 seqkit| \\
 0.12.1| \\
 Seqkit is a tool for manipulating fasta and fastq files.|

 **50** | \\
 samtools| \\
 1.10.2| \\
 suite of programs for interacting with high-throughput sequencing data|

 **51** | \\
 salmon| \\
 1.2.1| \\
 Is a tool for quantifying the expression of transcripts using RNA-seq data.|

 **52** | \\
 RSEM| \\
 1.3.3| \\
 Tool for the quantification of RNA-seq data.|

 **53** | \\
 roary| \\
 1.7.7| \\
 Application for rapidly constructing pan genomes from large numbers of prokaryote sample|

 **54** | \\
 racon| \\
 1.4.16| \\
 Consensus sequence|

 **55** | \\
 quast| \\
 5.1.0rc1| \\
 Quality Assessment Tool for Genome Assemblies|

 **56** | \\
 pyani| \\
 0.2.10| \\
 a Python3 module that provides support for calculating average nucleotide identity (ANI)|

 **57** | \\
 prokka| \\
 1.14.6| \\
 tool for the rapid annotation of prokaryotic genomes|

 **58** | \\
 prodigal| \\
 2.6.3| \\
 Prodigal is an unsupervised machine learning algorithm|

 **59** | \\
 prinseq| \\
 0.20.4| \\
 Tool that generates summary statistics of sequence and quality data and that is used to filter, reformat and trim …|

 **60** | \\
 prank| \\
 170427| \\
 Is a probabilistic multiple alignment program for DNA,|

 **61** | \\
 pplacer| \\
 1.1.alpha17| \\
 Places query sequences on a fixed reference phylogenetic tree to maximize phylogenetic likelihood or posterior probability according to a reference …|

 **62** | \\
 htslib| \\
 1.10.2| \\
 An implementation of a unified C library for accessing common file formats, such as SAM, CRAM and VCF, used for high-throughput sequencing data, …|

 **63** | \\
 mash| \\
 2.2| \\
 Reduces large sequences and sequence sets to small, …|

 **64** | \\
 mafft| \\
 7.470| \\
 is a multiple sequence alignment program for unix-like operating systems|

 **65** | \\
 ksnp| \\
 3.1.2| \\
 Finds single nucleotide polymorphisms (SNPs) in whole genome data.|

 **66** | \\
 krona| \\
 2.7.1| \\
 powerful metagenomic visualization tool|

 **67** | \\
 kaiju| \\
 1.7.3| \\
 program for the taxonomic classification of high-throughput sequencing reads.|

 **68** | \\
 jellyfish| \\
 2.3.0| \\
 tool for fast, memory-efficient counting of k-mers in DNA.|

 **69** | \\
 jdk| \\
 8.0_41| \\
 Java Develop ToolKit|

 **70** | \\
 jdk| \\
 14.0.1| \\
 Java Develop ToolKit|

 **71** | \\
 jdk| \\
 11.28| \\
 Java Develop ToolKit|

 **72** | \\
 infernal| \\
 1.1.3| \\
 for searching DNA sequence databases for RNA structure and sequence similarities|

 **73** | \\
 pilon| \\
 1.23| \\
 an automated genome assembly improvement and variant detection tool|

 **74** | \\
 picard| \\
 2.23.1| \\
 a set of command line tools for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.|

 **75** | \\
 phyml| \\
 3.3.20190909| \\
 is a phylogeny software based on the maximum-likelihood principle|

 **76** | \\
 phylip| \\
 3.697| \\
 a free package of programs for inferring phylogenies|

 **77** | \\
 parallel| \\
 20200622| \\
 Parallel is an indispensible tool for speeding up bioinformatics. It allows you to easily parallelize commands|

 **78** | \\
 paml| \\
 4.9| \\
 a package of programs for phylogenetic analyses of DNA or protein sequences using maximum likelihood.|

 **79** | \\
 ncftp| \\
 3.2.6| \\
 cliente ftp|

 **80** | \\
 muscle| \\
 3.8.31| \\
 A program to create multiple sequence alignments of a large number of sequences|

 **81** | \\
 MUMmer| \\
 3.23| \\
 an open source software package for the rapid alignment of very large DNA and amino acid sequences|

 **82** | \\
 mothur| \\
 1.44.1| \\
 a single resource to analyze molecular data that is used by microbial ecologists|

 **83** | \\
 minimap2| \\
 2.17| \\
 pairwise alignment for nucleotide sequences.|

 **84** | \\
 miniconda| \\
 4.8.3| \\
 python minimalist|

 **85** | \\
 MCL| \\
 14-137| \\
 a cluster algorithm for graphs|

 **86** | \\
 MinCED| \\
 0.4.2| \\
 program to find Clustered Regularly Interspaced Short .|

 **87** | \\
 fastqc| \\
 0.11.9| \\
 a quality control application for high throughput sequence data.|

 **88** | \\
 fasttree| \\
 2.1.11| \\
 FastTree infers approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences|

 **89** | \\
 Gblocks| \\
 0.91b| \\
 computer program written in ANSI C language that eliminates poorly aligned positions and divergent regions of an alignment of DNA or protein|

 **90** | \\
 go| \\
 1.14.4| \\
 compilador de lenguaje GO|
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