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software_bioinformatics [2020/11/24 14:40]
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software_bioinformatics [2024/05/11 03:56] (current)
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-====== ​Aplicaciones Científicas ​======+====== ​Software y librerías disponibles ​======
  
-<font 14px/​inherit;;​inherit;;​inherit>​Bioinformatics,​ Chemistry, Physics, etc</​font>​+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 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
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-| \\ +| \\ **#** | \\ **Aplicación** | \\ **Versión** | \\ **Descripción** |
-   **#** | \\ +
-   **Aplicación** | \\ +
-   **Versión** | \\ +
-   **Descripción** |+
 |**A** | | | | |**A** | | | |
-| |aragorn|1.2.38|tRNA (and tmRNA) detection| +| |aragorn|1.2.36|A software tool for predicting ​tRNA genes in DNA sequences, used for annotating genomes ​and identifying transfer RNA genes with high accuracy.|
-| |arb|6.0.6|Phylogenetic analysis of rRNA and other biological sequences such as amino acids| +
-| |ascp|3.9.9|–|+
 |**B** | | | | |**B** | | | |
-| |bowtie2|0.7.17|software ​package ​for mapping low-divergent sequences against a large reference genome, such as the human genome| +| |barrnap|0.9|software ​tool for predicting ribosomal RNA (rRNAgenes in DNA sequencesused for annotating genomes and identifying rRNA genes with high accuracy.| 
-| |bwa|2.4.1|alineación de secuencias y el análisis de secuencias en bioinformática| +| |bedtools|2.27.1|A powerful suite of tools for genomic ​analysis, providing functionality for the manipulation,​ comparison, ​and annotation ​of genomic intervals stored in BED format
-| |blast+|2.9.0|Alineamiento de secuencias de tipo local, ya sea de ADN, ARN o de proteínas| +| |bcftools|1.8|Set of utilities ​for variant ​calling ​and manipulation ​of variant call format (VCF) files in genomics research.
-| |blast+|2.10.0(default)|Alineamiento de secuencias de tipo localya sea de ADN, ARN o de proteínas| +| |bowtie2|2.5.3|A fast and memory-efficient alignment tool for mapping DNA sequencing reads to a reference genome
-| |blast|2.2.26|Alineamiento de secuencias de tipo local, ya sea de ADN, ARN o de proteínas+| |bzip2|1.0.8|A compression utility and file format used to compress and decompress files, known for its high compression ratio and efficient compression algorithms|
-| |bedtools|2.29.2|swiss-army knife of tools for a wide-range of genomics ​analysis ​tasks| +
-| |bedops|2.4.38|highly scalable ​and easily-parallelizable genome analysis toolkit| +
-| |beagle-lib|3.1.2|high-performance library that can perform the core calculations at the heart of most Bayesian and Maximum Likelihood phylogenetics+
-| |bcftools|1.10.2|set of utilities ​that manipulate ​variant ​calls| +
-| |bbtools|38.86|suite of fast, multithreaded bioinformatics tools designed for analysis of DNA and RNA sequence data| +
-| |barrnap|0.9|predicts the location ​of ribosomal RNA genes in genomes+
-| |bamtools|2.5.1|toolkit ​for handling BAM files.+
-| | | | |+
 |**C** | | | | |**C** | | | |
-| |cufflinks|2.10|finds and removes adapter sequencesprimers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads+| |cd-hit|4.6.8-2017-0621|A fast and efficient clustering tool for sequence analysiscommonly used in bioinformatics to identify ​and remove redundancy within large sets of sequences.
-| |circos|2.2.1|Transcriptome assembly and differential expression analysis ​for RNA-Seq.| +| |cmake|3.15.4|Cross-platform build system generator, widely used for managing the build process of software projects.| 
-| |cutadapt|0.69-9|for visualizing data and informationIt visualizes data in a circular layout+| |cmake|3.20.6|Cross-platform build system generator, widely used for managing the build process of software projects.| 
-| |checkm|1.1.2|set of tools for assessing the quality of genomes recovered ​from isolates, single cells, or metagenomes+| |cpanm|1.7047-perl-5.38.2|Lightweight command-line tool for installing Perl modules ​from CPAN.
-| |cdhit|4.8.1|Takes a fasta format sequence database as input and produces ​set of '​non-redundant'​ (nr)…| +| |curl|8.7.1|A command-line tool and library for transferring data with URLs, supporting ​wide range of protocols including HTTP, HTTPS, FTP, and more.|
-| |canu|1.9|Fork of the Celera Assembler designed for high-noise single-molecule sequencing| +
-| | | | | +
-| | | | |+
 |**D** | | | | |**D** | | | |
-| |diamond|0.9.35|molecular and crystal structure visualization software| 
 |**E** | | | | |**E** | | | |
 +| |expat|2.6.2|Fast,​ lightweight,​ and robust XML parser library written in C.|
 |**F** | | | | |**F** | | | |
 +| |fastqc|0.12.1|A quality control tool for high-throughput sequencing data, commonly used to assess the quality of raw sequence data generated by next-generation sequencing (NGS) platforms|
 +| |fasttree|2.1.10|A tool for inferring approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences|
 +| |fftw|3.3.10|FFTW (Fastest Fourier Transform in the West) is a highly efficient library for computing discrete Fourier transforms.|
 +| |fftw|3.3.10-openmp-threads|FFTW (Fastest Fourier Transform in the West) is a highly efficient library for computing discrete Fourier transforms.|
 |**G** | | | | |**G** | | | |
-| |gromacs|2019.4|Modelamiento ​Molecular|+| |gromacs|2019.4-fftw-3.3.10-openmpi-4.1.1|Molecular ​dynamics simulation software widely used for biomolecular studies.| 
 +| |gromacs|2024.1-fftw-3.3.10-openmpi-4.1.6|Molecular dynamics simulation software widely used for biomolecular studies.|
 |**H** | | | | |**H** | | | |
-| |hmmer|2.3.2|biosequence ​analysis ​using profile hidden Markov models .+| |harvest|1.1.2|A suite of tools for analyzing and visualizing genomic data, it provides functionalities for genome alignment, synteny ​analysis, and visualization of genomic features
-| |hmmer|3.1b1|biosequence analysis using profile hidden Markov models ​.| +| |hdf5|1.14.4-2|HDF5 (Hierarchical Data Format version 5): A versatile and high-performance file format and library for managing and storing large and complex datasets
-| |hmmer|3.1b2|biosequence analysis ​using profile hidden Markov models ​.| +| |hmmer|3.4|A software suite for searching sequence databases ​using profile hidden Markov models ​(HMMs), used for protein sequence ​analysis, homology detection, and functional annotation.|
-| |hmmer|3.2.1|biosequence ​analysis ​using profile hidden Markov models ​.+
-| | | | |+
 |**I** | | | | |**I** | | | |
 +| |infernal|1.1.5|A software suite for searching sequence databases using covariance models (CMs) and profile stochastic context-free grammars (SCFGs).|
 |**J** | | | | |**J** | | | |
 +| |jasper|4.2.4|JPEG-2000 reference software, commonly used for encoding and decoding images in the JPEG-2000 format, with support for various image compression and decompression functionalities.|
 +| |jdk|8.0_41|JDK (Java Development Kit): A set of software tools and libraries for developing Java applications,​ including compilers, debuggers, and class libraries|
 +| |jdk|17.0.10|JDK (Java Development Kit): A set of software tools and libraries for developing Java applications,​ including compilers, debuggers, and class libraries|
 |**K** | | | | |**K** | | | |
 |**L** | | | | |**L** | | | |
 +| |lammps|17Apr2024-openmpi-4.1.6|Large-scale Atomic/​Molecular Massively Parallel Simulator, a versatile molecular dynamics software package for simulating a wide range of materials and biological systems.|
 +| |libdb|5.3.28|A library providing high-performance embedded database functionality,​ commonly used in applications requiring efficient data storage and retrieval.|
 +| |libidn|1.33|A library for handling Internationalized Domain Names (IDN), providing support for encoding and decoding domain names containing non-ASCII characters.|
 +| |libncurses|6.5|A programming library that provides an API for creating text-based user interfaces (TUI) in a terminal environment|
 +| |libnsl|1.2.0|A library providing support for Network Services Library (NSL) functions, including name and address resolution, used for network communication in Unix-based systems.|
 +| |libnsl|1.3.0|A library providing support for Network Services Library (NSL) functions, including name and address resolution, used for network communication in Unix-based systems.|
 +| |libnsl|2.0.1|A library providing support for Network Services Library (NSL) functions, including name and address resolution, used for network communication in Unix-based systems.|
 +| |libpng|1.6.43|A platform-independent library that contains C functions for handling PNG images.|
 +| |libreadline|8.2|A library for creating interactive command-line interfaces (CLI) with advanced line-editing capabilities,​ including command history, completion, and customizable key bindings.|
 +| |libtirpc|1.0.2|A library providing transport-independent RPC (Remote Procedure Call) protocol support, facilitating communication between distributed applications over a network.|
 +| |libtirpc|1.3.4|A library providing transport-independent RPC (Remote Procedure Call) protocol support, facilitating communication between distributed applications over a network.|
 |**M** | | | | |**M** | | | |
 +| |mafft|7.310|A versatile and accurate multiple sequence alignment program, widely used for aligning nucleotide and protein sequences to infer evolutionary relationships.|
 +| |mcl|14-137|MCL (Markov Cluster Algorithm): A graph clustering algorithm used to identify clusters in large networks or graphs.|
 +| |minced|0.4.2|Is a program to find Clustered Regularly Interspaced Short Palindromic Repeats (CRISPRs) in full genomes or environmental datasets such as assembled contigs from metagenomes.|
 +| |miniconda3|24.3.0|Lightweight distribution of the Conda package manager and Python environment|
 |**N** | | | | |**N** | | | |
-| |Namd2|2019-11-27-multicore|Modelamiento Molecular|+| |ncbi-blast|2.6.0-libnsl-1.2.0-libidn-1.33|BLAST finds regions of similarity between biological sequences. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance.| 
 +| |ncbi-blast ​ |2.13.0|BLAST finds regions of similarity between biological sequences. The program compares nucleotide or protein sequences to sequence databases and calculates the statistical significance.| 
 +| |netcdf ​ |c-4.7.3-fortran-4.5.2|NetCDF (Network Common Data Form): A file format and set of software libraries used for storing and accessing multidimensional scientific data| 
 +|**O** | | | | 
 +| |openfoam|v2312|Open-source computational fluid dynamics (CFD) software package for simulating complex fluid flows.| 
 +| |openmpi|4.1.1|Open-source implementation of the Message Passing Interface (MPI) standard for parallel computing, enabling efficient communication among distributed processes.| 
 +| |openmpi|4.1.6|Open-source implementation of the Message Passing Interface (MPI) standard for parallel computing, enabling efficient communication among distributed processes.|
 |**P** | | | | |**P** | | | |
 +| |parallel|20160722|A shell tool for executing jobs in parallel, allowing for efficient and concurrent execution of tasks across multiple cores or machines.|
 +| |parsnp|2.0.5|Tool for rapid core-genome alignment and SNP detection|
 +| |pcre|2.10.43|PCRE (Perl Compatible Regular Expressions):​ A library for implementing regular expression pattern matching using syntax similar to Perl|
 +| |perl|5.38.2|High-level,​ general-purpose programming language known for its versatility in text processing and system administration tasks.|
 +| |prank|170427|A tool for the rapid and accurate generation of phylogenetic trees based on sequence alignment data|
 +| |prodigal|2.6.3|A software tool for predicting protein-coding genes in DNA sequences, used for annotating genomes and identifying protein-coding genes with high accuracy.|
 +| |prokka|1.14.6|A software tool for annotating bacterial, archaeal, and viral genomes, used for predicting protein-coding genes, identifying non-coding RNAs, and annotating genomic features with functional information.|
 +| |python|3.12.1|High-level programming language, widely used for scripting, web development,​ data analysis, and more.|
 |**Q** | | | | |**Q** | | | |
 +| |qiime2|amplicon-2024.2-py38|A bioinformatics software package for analyzing and visualizing microbial community data generated from high-throughput sequencing technologies|
 |**R** | | | | |**R** | | | |
-| |R|3.6.1|Analísis Estadistico+| |R|4.4.0|A programming language and environment for statistical computing and graphics, widely used in data analysis, statistical modeling, and visualization| 
-| | | | |+| |roary|3.12|A tool for rapidly identifying core and accessory genes from bacterial genome assemblies, used in comparative genomics studies to analyze bacterial pan-genomes and assess genomic diversity.
 +|**S** | | | | 
 +| |samtools|1.9|Suite of programs for interacting with high-throughput sequencing data| 
 +| |singularity|4.1.0|Containerization platform designed for HPC environments,​ facilitating reproducibility and portability of software stacks.| 
 +|**T** | | | | 
 +| |tabix|0.2.5|Tool for indexing and querying large tab-delimited text files, commonly used in genomics research for efficient retrieval of specific genomic regions.| 
 +| |table2asn|1.28.943|A command-line tool for converting structured data tables into GenBank submission files, used for annotating DNA sequences and preparing submissions to the GenBank database.| 
 +|**U** | | | | 
 +|**V** | | | |
 |**W** | | | | |**W** | | | |
-| |WRF|3.9.1|Mesoscale numerical weather prediction| 
-| |WRF|4.0|Mesoscale numerical weather prediction| 
 |**X** | | | | |**X** | | | |
-\\ +|**Y** | | | | 
-   **6** | \\ +|**Z** | | | | 
-   ​netcdf/​c\\ +| |zlib|1.2.13|A ​versatile compression ​library for data compression ​and decompression.|
-   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| \\ +
-   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| +
-| \\ +
-   ​**91** | \\ +
-   ​gtdbtk| \\ +
-   ​1.2.0| \\ +
-   a toolkit to classify genomes with the Genome Taxonomy Database, B|+
  
  
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  • Last modified: 2020/11/24 14:40
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