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hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets

Understanding how the genome is shaped by selective processes forms an integral part of modern biology. However, as genomic datasets continue to grow larger it is becoming increasingly difficult to apply traditional statistics for detecting signatures of selection to these cohorts. There is therefor...

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Detalles Bibliográficos
Autores principales: Maclean, Colin A., Chue Hong, Neil P., Prendergast, James G.D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4651233/
https://www.ncbi.nlm.nih.gov/pubmed/26248562
http://dx.doi.org/10.1093/molbev/msv172
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author Maclean, Colin A.
Chue Hong, Neil P.
Prendergast, James G.D.
author_facet Maclean, Colin A.
Chue Hong, Neil P.
Prendergast, James G.D.
author_sort Maclean, Colin A.
collection PubMed
description Understanding how the genome is shaped by selective processes forms an integral part of modern biology. However, as genomic datasets continue to grow larger it is becoming increasingly difficult to apply traditional statistics for detecting signatures of selection to these cohorts. There is therefore a pressing need for the development of the next generation of computational and analytical tools for detecting signatures of selection in large genomic datasets. Here, we present hapbin, an efficient multithreaded implementation of extended haplotype homzygosity-based statistics for detecting selection, which is up to 3,400 times faster than the current fastest implementations of these algorithms.
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spelling pubmed-46512332015-11-25 hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets Maclean, Colin A. Chue Hong, Neil P. Prendergast, James G.D. Mol Biol Evol Resources Understanding how the genome is shaped by selective processes forms an integral part of modern biology. However, as genomic datasets continue to grow larger it is becoming increasingly difficult to apply traditional statistics for detecting signatures of selection to these cohorts. There is therefore a pressing need for the development of the next generation of computational and analytical tools for detecting signatures of selection in large genomic datasets. Here, we present hapbin, an efficient multithreaded implementation of extended haplotype homzygosity-based statistics for detecting selection, which is up to 3,400 times faster than the current fastest implementations of these algorithms. Oxford University Press 2015-11 2015-08-06 /pmc/articles/PMC4651233/ /pubmed/26248562 http://dx.doi.org/10.1093/molbev/msv172 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Resources
Maclean, Colin A.
Chue Hong, Neil P.
Prendergast, James G.D.
hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets
title hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets
title_full hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets
title_fullStr hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets
title_full_unstemmed hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets
title_short hapbin: An Efficient Program for Performing Haplotype-Based Scans for Positive Selection in Large Genomic Datasets
title_sort hapbin: an efficient program for performing haplotype-based scans for positive selection in large genomic datasets
topic Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4651233/
https://www.ncbi.nlm.nih.gov/pubmed/26248562
http://dx.doi.org/10.1093/molbev/msv172
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