Cargando…

VSEARCH: a versatile open source tool for metagenomics

BACKGROUND: VSEARCH is an open source and free of charge multithreaded 64-bit tool for processing and preparing metagenomics, genomics and population genomics nucleotide sequence data. It is designed as an alternative to the widely used USEARCH tool (Edgar, 2010) for which the source code is not pub...

Descripción completa

Detalles Bibliográficos
Autores principales: Rognes, Torbjørn, Flouri, Tomáš, Nichols, Ben, Quince, Christopher, Mahé, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075697/
https://www.ncbi.nlm.nih.gov/pubmed/27781170
http://dx.doi.org/10.7717/peerj.2584
_version_ 1782461914431881216
author Rognes, Torbjørn
Flouri, Tomáš
Nichols, Ben
Quince, Christopher
Mahé, Frédéric
author_facet Rognes, Torbjørn
Flouri, Tomáš
Nichols, Ben
Quince, Christopher
Mahé, Frédéric
author_sort Rognes, Torbjørn
collection PubMed
description BACKGROUND: VSEARCH is an open source and free of charge multithreaded 64-bit tool for processing and preparing metagenomics, genomics and population genomics nucleotide sequence data. It is designed as an alternative to the widely used USEARCH tool (Edgar, 2010) for which the source code is not publicly available, algorithm details are only rudimentarily described, and only a memory-confined 32-bit version is freely available for academic use. METHODS: When searching nucleotide sequences, VSEARCH uses a fast heuristic based on words shared by the query and target sequences in order to quickly identify similar sequences, a similar strategy is probably used in USEARCH. VSEARCH then performs optimal global sequence alignment of the query against potential target sequences, using full dynamic programming instead of the seed-and-extend heuristic used by USEARCH. Pairwise alignments are computed in parallel using vectorisation and multiple threads. RESULTS: VSEARCH includes most commands for analysing nucleotide sequences available in USEARCH version 7 and several of those available in USEARCH version 8, including searching (exact or based on global alignment), clustering by similarity (using length pre-sorting, abundance pre-sorting or a user-defined order), chimera detection (reference-based or de novo), dereplication (full length or prefix), pairwise alignment, reverse complementation, sorting, and subsampling. VSEARCH also includes commands for FASTQ file processing, i.e., format detection, filtering, read quality statistics, and merging of paired reads. Furthermore, VSEARCH extends functionality with several new commands and improvements, including shuffling, rereplication, masking of low-complexity sequences with the well-known DUST algorithm, a choice among different similarity definitions, and FASTQ file format conversion. VSEARCH is here shown to be more accurate than USEARCH when performing searching, clustering, chimera detection and subsampling, while on a par with USEARCH for paired-ends read merging. VSEARCH is slower than USEARCH when performing clustering and chimera detection, but significantly faster when performing paired-end reads merging and dereplication. VSEARCH is available at https://github.com/torognes/vsearch under either the BSD 2-clause license or the GNU General Public License version 3.0. DISCUSSION: VSEARCH has been shown to be a fast, accurate and full-fledged alternative to USEARCH. A free and open-source versatile tool for sequence analysis is now available to the metagenomics community.
format Online
Article
Text
id pubmed-5075697
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher PeerJ Inc.
record_format MEDLINE/PubMed
spelling pubmed-50756972016-10-25 VSEARCH: a versatile open source tool for metagenomics Rognes, Torbjørn Flouri, Tomáš Nichols, Ben Quince, Christopher Mahé, Frédéric PeerJ Biodiversity BACKGROUND: VSEARCH is an open source and free of charge multithreaded 64-bit tool for processing and preparing metagenomics, genomics and population genomics nucleotide sequence data. It is designed as an alternative to the widely used USEARCH tool (Edgar, 2010) for which the source code is not publicly available, algorithm details are only rudimentarily described, and only a memory-confined 32-bit version is freely available for academic use. METHODS: When searching nucleotide sequences, VSEARCH uses a fast heuristic based on words shared by the query and target sequences in order to quickly identify similar sequences, a similar strategy is probably used in USEARCH. VSEARCH then performs optimal global sequence alignment of the query against potential target sequences, using full dynamic programming instead of the seed-and-extend heuristic used by USEARCH. Pairwise alignments are computed in parallel using vectorisation and multiple threads. RESULTS: VSEARCH includes most commands for analysing nucleotide sequences available in USEARCH version 7 and several of those available in USEARCH version 8, including searching (exact or based on global alignment), clustering by similarity (using length pre-sorting, abundance pre-sorting or a user-defined order), chimera detection (reference-based or de novo), dereplication (full length or prefix), pairwise alignment, reverse complementation, sorting, and subsampling. VSEARCH also includes commands for FASTQ file processing, i.e., format detection, filtering, read quality statistics, and merging of paired reads. Furthermore, VSEARCH extends functionality with several new commands and improvements, including shuffling, rereplication, masking of low-complexity sequences with the well-known DUST algorithm, a choice among different similarity definitions, and FASTQ file format conversion. VSEARCH is here shown to be more accurate than USEARCH when performing searching, clustering, chimera detection and subsampling, while on a par with USEARCH for paired-ends read merging. VSEARCH is slower than USEARCH when performing clustering and chimera detection, but significantly faster when performing paired-end reads merging and dereplication. VSEARCH is available at https://github.com/torognes/vsearch under either the BSD 2-clause license or the GNU General Public License version 3.0. DISCUSSION: VSEARCH has been shown to be a fast, accurate and full-fledged alternative to USEARCH. A free and open-source versatile tool for sequence analysis is now available to the metagenomics community. PeerJ Inc. 2016-10-18 /pmc/articles/PMC5075697/ /pubmed/27781170 http://dx.doi.org/10.7717/peerj.2584 Text en ©2016 Rognes et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biodiversity
Rognes, Torbjørn
Flouri, Tomáš
Nichols, Ben
Quince, Christopher
Mahé, Frédéric
VSEARCH: a versatile open source tool for metagenomics
title VSEARCH: a versatile open source tool for metagenomics
title_full VSEARCH: a versatile open source tool for metagenomics
title_fullStr VSEARCH: a versatile open source tool for metagenomics
title_full_unstemmed VSEARCH: a versatile open source tool for metagenomics
title_short VSEARCH: a versatile open source tool for metagenomics
title_sort vsearch: a versatile open source tool for metagenomics
topic Biodiversity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075697/
https://www.ncbi.nlm.nih.gov/pubmed/27781170
http://dx.doi.org/10.7717/peerj.2584
work_keys_str_mv AT rognestorbjørn vsearchaversatileopensourcetoolformetagenomics
AT flouritomas vsearchaversatileopensourcetoolformetagenomics
AT nicholsben vsearchaversatileopensourcetoolformetagenomics
AT quincechristopher vsearchaversatileopensourcetoolformetagenomics
AT mahefrederic vsearchaversatileopensourcetoolformetagenomics