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Rapid haplotype inference for nuclear families

Hapi is a new dynamic programming algorithm that ignores uninformative states and state transitions in order to efficiently compute minimum-recombinant and maximum likelihood haplotypes. When applied to a dataset containing 103 families, Hapi performs 3.8 and 320 times faster than state-of-the-art a...

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Detalles Bibliográficos
Autores principales: Williams, Amy L, Housman, David E, Rinard, Martin C, Gifford, David K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218664/
https://www.ncbi.nlm.nih.gov/pubmed/21034477
http://dx.doi.org/10.1186/gb-2010-11-10-r108
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author Williams, Amy L
Housman, David E
Rinard, Martin C
Gifford, David K
author_facet Williams, Amy L
Housman, David E
Rinard, Martin C
Gifford, David K
author_sort Williams, Amy L
collection PubMed
description Hapi is a new dynamic programming algorithm that ignores uninformative states and state transitions in order to efficiently compute minimum-recombinant and maximum likelihood haplotypes. When applied to a dataset containing 103 families, Hapi performs 3.8 and 320 times faster than state-of-the-art algorithms. Because Hapi infers both minimum-recombinant and maximum likelihood haplotypes and applies to related individuals, the haplotypes it infers are highly accurate over extended genomic distances.
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spelling pubmed-32186642011-11-18 Rapid haplotype inference for nuclear families Williams, Amy L Housman, David E Rinard, Martin C Gifford, David K Genome Biol Method Hapi is a new dynamic programming algorithm that ignores uninformative states and state transitions in order to efficiently compute minimum-recombinant and maximum likelihood haplotypes. When applied to a dataset containing 103 families, Hapi performs 3.8 and 320 times faster than state-of-the-art algorithms. Because Hapi infers both minimum-recombinant and maximum likelihood haplotypes and applies to related individuals, the haplotypes it infers are highly accurate over extended genomic distances. BioMed Central 2010 2010-10-29 /pmc/articles/PMC3218664/ /pubmed/21034477 http://dx.doi.org/10.1186/gb-2010-11-10-r108 Text en Copyright ©2010 Williams et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Method
Williams, Amy L
Housman, David E
Rinard, Martin C
Gifford, David K
Rapid haplotype inference for nuclear families
title Rapid haplotype inference for nuclear families
title_full Rapid haplotype inference for nuclear families
title_fullStr Rapid haplotype inference for nuclear families
title_full_unstemmed Rapid haplotype inference for nuclear families
title_short Rapid haplotype inference for nuclear families
title_sort rapid haplotype inference for nuclear families
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218664/
https://www.ncbi.nlm.nih.gov/pubmed/21034477
http://dx.doi.org/10.1186/gb-2010-11-10-r108
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