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software_bioinformatics [2020/11/24 14:40]
admin old revision restored (2020/11/08 22:22)
software_bioinformatics [2024/05/11 03:56] (current)
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-====== ​Aplicaciones Científicas ​======+====== ​Software y librerías disponibles ​======
  
 Bioinformatics,​ Chemistry, Physics, etc Bioinformatics,​ Chemistry, Physics, etc
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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** | | | |
-\\ **6** | \\ netcdf/c\\ 4.7.3\\ Network Common Data Form+|**Y** | | | | 
-\\ **7** | \\ netcdf/​fortran\\ 4.5.2\\ Network Common Data Form+|**Z** | | | | 
-\\ **8** \\ quantum-espresso/​schrodinger\\ 6.4.1-2019-4| \\ Modelamiento Molecular| +| |zlib|1.2.13|A ​versatile compression ​library for data compression ​and decompression.|
-| \\ **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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