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Genome Scans for Detecting Footprints of Local Adaptation Using a Bayesian Factor Model
There is a considerable impetus in population genomics to pinpoint loci involved in local adaptation. A powerful approach to find genomic regions subject to local adaptation is to genotype numerous molecular markers and look for outlier loci. One of the most common approaches for selection scans is...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137708/ https://www.ncbi.nlm.nih.gov/pubmed/24899666 http://dx.doi.org/10.1093/molbev/msu182 |
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author | Duforet-Frebourg, Nicolas Bazin, Eric Blum, Michael G.B. |
author_facet | Duforet-Frebourg, Nicolas Bazin, Eric Blum, Michael G.B. |
author_sort | Duforet-Frebourg, Nicolas |
collection | PubMed |
description | There is a considerable impetus in population genomics to pinpoint loci involved in local adaptation. A powerful approach to find genomic regions subject to local adaptation is to genotype numerous molecular markers and look for outlier loci. One of the most common approaches for selection scans is based on statistics that measure population differentiation such as F(ST). However, there are important caveats with approaches related to F(ST) because they require grouping individuals into populations and they additionally assume a particular model of population structure. Here, we implement a more flexible individual-based approach based on Bayesian factor models. Factor models capture population structure with latent variables called factors, which can describe clustering of individuals into populations or isolation-by-distance patterns. Using hierarchical Bayesian modeling, we both infer population structure and identify outlier loci that are candidates for local adaptation. In order to identify outlier loci, the hierarchical factor model searches for loci that are atypically related to population structure as measured by the latent factors. In a model of population divergence, we show that it can achieve a 2-fold or more reduction of false discovery rate compared with the software BayeScan or with an F(ST) approach. We show that our software can handle large data sets by analyzing the single nucleotide polymorphisms of the Human Genome Diversity Project. The Bayesian factor model is implemented in the open-source PCAdapt software. |
format | Online Article Text |
id | pubmed-4137708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41377082014-08-21 Genome Scans for Detecting Footprints of Local Adaptation Using a Bayesian Factor Model Duforet-Frebourg, Nicolas Bazin, Eric Blum, Michael G.B. Mol Biol Evol Methods There is a considerable impetus in population genomics to pinpoint loci involved in local adaptation. A powerful approach to find genomic regions subject to local adaptation is to genotype numerous molecular markers and look for outlier loci. One of the most common approaches for selection scans is based on statistics that measure population differentiation such as F(ST). However, there are important caveats with approaches related to F(ST) because they require grouping individuals into populations and they additionally assume a particular model of population structure. Here, we implement a more flexible individual-based approach based on Bayesian factor models. Factor models capture population structure with latent variables called factors, which can describe clustering of individuals into populations or isolation-by-distance patterns. Using hierarchical Bayesian modeling, we both infer population structure and identify outlier loci that are candidates for local adaptation. In order to identify outlier loci, the hierarchical factor model searches for loci that are atypically related to population structure as measured by the latent factors. In a model of population divergence, we show that it can achieve a 2-fold or more reduction of false discovery rate compared with the software BayeScan or with an F(ST) approach. We show that our software can handle large data sets by analyzing the single nucleotide polymorphisms of the Human Genome Diversity Project. The Bayesian factor model is implemented in the open-source PCAdapt software. Oxford University Press 2014-09 2014-06-03 /pmc/articles/PMC4137708/ /pubmed/24899666 http://dx.doi.org/10.1093/molbev/msu182 Text en © The Author 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Duforet-Frebourg, Nicolas Bazin, Eric Blum, Michael G.B. Genome Scans for Detecting Footprints of Local Adaptation Using a Bayesian Factor Model |
title | Genome Scans for Detecting Footprints of Local Adaptation Using a Bayesian Factor Model |
title_full | Genome Scans for Detecting Footprints of Local Adaptation Using a Bayesian Factor Model |
title_fullStr | Genome Scans for Detecting Footprints of Local Adaptation Using a Bayesian Factor Model |
title_full_unstemmed | Genome Scans for Detecting Footprints of Local Adaptation Using a Bayesian Factor Model |
title_short | Genome Scans for Detecting Footprints of Local Adaptation Using a Bayesian Factor Model |
title_sort | genome scans for detecting footprints of local adaptation using a bayesian factor model |
topic | Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137708/ https://www.ncbi.nlm.nih.gov/pubmed/24899666 http://dx.doi.org/10.1093/molbev/msu182 |
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