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FastQ Screen: A tool for multi-genome mapping and quality control

DNA sequencing analysis typically involves mapping reads to just one reference genome. Mapping against multiple genomes is necessary, however, when the genome of origin requires confirmation. Mapping against multiple genomes is also advisable for detecting contamination or for identifying sample swa...

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Detalles Bibliográficos
Autores principales: Wingett, Steven W., Andrews, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124377/
https://www.ncbi.nlm.nih.gov/pubmed/30254741
http://dx.doi.org/10.12688/f1000research.15931.2
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author Wingett, Steven W.
Andrews, Simon
author_facet Wingett, Steven W.
Andrews, Simon
author_sort Wingett, Steven W.
collection PubMed
description DNA sequencing analysis typically involves mapping reads to just one reference genome. Mapping against multiple genomes is necessary, however, when the genome of origin requires confirmation. Mapping against multiple genomes is also advisable for detecting contamination or for identifying sample swaps which, if left undetected, may lead to incorrect experimental conclusions. Consequently, we present FastQ Screen, a tool to validate the origin of DNA samples by quantifying the proportion of reads that map to a panel of reference genomes. FastQ Screen is intended to be used routinely as a quality control measure and for analysing samples in which the origin of the DNA is uncertain or has multiple sources.
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spelling pubmed-61243772018-09-24 FastQ Screen: A tool for multi-genome mapping and quality control Wingett, Steven W. Andrews, Simon F1000Res Software Tool Article DNA sequencing analysis typically involves mapping reads to just one reference genome. Mapping against multiple genomes is necessary, however, when the genome of origin requires confirmation. Mapping against multiple genomes is also advisable for detecting contamination or for identifying sample swaps which, if left undetected, may lead to incorrect experimental conclusions. Consequently, we present FastQ Screen, a tool to validate the origin of DNA samples by quantifying the proportion of reads that map to a panel of reference genomes. FastQ Screen is intended to be used routinely as a quality control measure and for analysing samples in which the origin of the DNA is uncertain or has multiple sources. F1000 Research Limited 2018-09-17 /pmc/articles/PMC6124377/ /pubmed/30254741 http://dx.doi.org/10.12688/f1000research.15931.2 Text en Copyright: © 2018 Wingett SW and Andrews S http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Software Tool Article
Wingett, Steven W.
Andrews, Simon
FastQ Screen: A tool for multi-genome mapping and quality control
title FastQ Screen: A tool for multi-genome mapping and quality control
title_full FastQ Screen: A tool for multi-genome mapping and quality control
title_fullStr FastQ Screen: A tool for multi-genome mapping and quality control
title_full_unstemmed FastQ Screen: A tool for multi-genome mapping and quality control
title_short FastQ Screen: A tool for multi-genome mapping and quality control
title_sort fastq screen: a tool for multi-genome mapping and quality control
topic Software Tool Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6124377/
https://www.ncbi.nlm.nih.gov/pubmed/30254741
http://dx.doi.org/10.12688/f1000research.15931.2
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