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Simultaneous alignment of short reads against multiple genomes

Genome resequencing with short reads generally relies on alignments against a single reference. GenomeMapper supports simultaneous mapping of short reads against multiple genomes by integrating related genomes (e.g., individuals of the same species) into a single graph structure. It constitutes the...

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Detalles Bibliográficos
Autores principales: Schneeberger, Korbinian, Hagmann, Jörg, Ossowski, Stephan, Warthmann, Norman, Gesing, Sandra, Kohlbacher, Oliver, Weigel, Detlef
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768987/
https://www.ncbi.nlm.nih.gov/pubmed/19761611
http://dx.doi.org/10.1186/gb-2009-10-9-r98
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author Schneeberger, Korbinian
Hagmann, Jörg
Ossowski, Stephan
Warthmann, Norman
Gesing, Sandra
Kohlbacher, Oliver
Weigel, Detlef
author_facet Schneeberger, Korbinian
Hagmann, Jörg
Ossowski, Stephan
Warthmann, Norman
Gesing, Sandra
Kohlbacher, Oliver
Weigel, Detlef
author_sort Schneeberger, Korbinian
collection PubMed
description Genome resequencing with short reads generally relies on alignments against a single reference. GenomeMapper supports simultaneous mapping of short reads against multiple genomes by integrating related genomes (e.g., individuals of the same species) into a single graph structure. It constitutes the first approach for handling multiple references and introduces representations for alignments against complex structures. Demonstrated benefits include access to polymorphisms that cannot be identified by alignments against the reference alone. Download GenomeMapper at .
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spelling pubmed-27689872009-10-28 Simultaneous alignment of short reads against multiple genomes Schneeberger, Korbinian Hagmann, Jörg Ossowski, Stephan Warthmann, Norman Gesing, Sandra Kohlbacher, Oliver Weigel, Detlef Genome Biol Software Genome resequencing with short reads generally relies on alignments against a single reference. GenomeMapper supports simultaneous mapping of short reads against multiple genomes by integrating related genomes (e.g., individuals of the same species) into a single graph structure. It constitutes the first approach for handling multiple references and introduces representations for alignments against complex structures. Demonstrated benefits include access to polymorphisms that cannot be identified by alignments against the reference alone. Download GenomeMapper at . BioMed Central 2009 2009-09-17 /pmc/articles/PMC2768987/ /pubmed/19761611 http://dx.doi.org/10.1186/gb-2009-10-9-r98 Text en Copyright © 2009 Schneeberger et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Software
Schneeberger, Korbinian
Hagmann, Jörg
Ossowski, Stephan
Warthmann, Norman
Gesing, Sandra
Kohlbacher, Oliver
Weigel, Detlef
Simultaneous alignment of short reads against multiple genomes
title Simultaneous alignment of short reads against multiple genomes
title_full Simultaneous alignment of short reads against multiple genomes
title_fullStr Simultaneous alignment of short reads against multiple genomes
title_full_unstemmed Simultaneous alignment of short reads against multiple genomes
title_short Simultaneous alignment of short reads against multiple genomes
title_sort simultaneous alignment of short reads against multiple genomes
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768987/
https://www.ncbi.nlm.nih.gov/pubmed/19761611
http://dx.doi.org/10.1186/gb-2009-10-9-r98
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