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A coalescent sampler successfully detects biologically meaningful population structure overlooked by F‐statistics

Assessing the geographic structure of populations has relied heavily on Sewell Wright's F‐statistics and their numerous analogues for many decades. However, it is well appreciated that, due to their nonlinear relationship with gene flow, F‐statistics frequently fail to reject the null model of...

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Autores principales: Crandall, Eric D., Toonen, Robert J., Selkoe, Kimberly A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346657/
https://www.ncbi.nlm.nih.gov/pubmed/30697337
http://dx.doi.org/10.1111/eva.12712
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author Crandall, Eric D.
Toonen, Robert J.
Selkoe, Kimberly A.
author_facet Crandall, Eric D.
Toonen, Robert J.
Selkoe, Kimberly A.
author_sort Crandall, Eric D.
collection PubMed
description Assessing the geographic structure of populations has relied heavily on Sewell Wright's F‐statistics and their numerous analogues for many decades. However, it is well appreciated that, due to their nonlinear relationship with gene flow, F‐statistics frequently fail to reject the null model of panmixia in species with relatively high levels of gene flow and large population sizes. Coalescent genealogy samplers instead allow a model‐selection approach to the characterization of population structure, thereby providing the opportunity for stronger inference. Here, we validate the use of coalescent samplers in a high gene flow context using simulations of a stepping‐stone model. In an example case study, we then re‐analyze genetic datasets from 41 marine species sampled from throughout the Hawaiian archipelago using coalescent model selection. Due to the archipelago's linear nature, it is expected that most species will conform to some sort of stepping‐stone model (leading to an expected pattern of isolation by distance), but F‐statistics have only supported this inference in ~10% of these datasets. Our simulation analysis shows that a coalescent sampler can make a correct inference of stepping‐stone gene flow in nearly 100% of cases where gene flow is ≤100 migrants per generation (equivalent to F (ST) = 0.002), while F‐statistics had mixed results. Our re‐analysis of empirical datasets found that nearly 70% of datasets with an unambiguous result fit a stepping‐stone model with varying population sizes and rates of gene flow, although 37% of datasets yielded ambiguous results. Together, our results demonstrate that coalescent samplers hold great promise for detecting weak but meaningful population structure, and defining appropriate management units.
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spelling pubmed-63466572019-01-29 A coalescent sampler successfully detects biologically meaningful population structure overlooked by F‐statistics Crandall, Eric D. Toonen, Robert J. Selkoe, Kimberly A. Evol Appl Original Articles Assessing the geographic structure of populations has relied heavily on Sewell Wright's F‐statistics and their numerous analogues for many decades. However, it is well appreciated that, due to their nonlinear relationship with gene flow, F‐statistics frequently fail to reject the null model of panmixia in species with relatively high levels of gene flow and large population sizes. Coalescent genealogy samplers instead allow a model‐selection approach to the characterization of population structure, thereby providing the opportunity for stronger inference. Here, we validate the use of coalescent samplers in a high gene flow context using simulations of a stepping‐stone model. In an example case study, we then re‐analyze genetic datasets from 41 marine species sampled from throughout the Hawaiian archipelago using coalescent model selection. Due to the archipelago's linear nature, it is expected that most species will conform to some sort of stepping‐stone model (leading to an expected pattern of isolation by distance), but F‐statistics have only supported this inference in ~10% of these datasets. Our simulation analysis shows that a coalescent sampler can make a correct inference of stepping‐stone gene flow in nearly 100% of cases where gene flow is ≤100 migrants per generation (equivalent to F (ST) = 0.002), while F‐statistics had mixed results. Our re‐analysis of empirical datasets found that nearly 70% of datasets with an unambiguous result fit a stepping‐stone model with varying population sizes and rates of gene flow, although 37% of datasets yielded ambiguous results. Together, our results demonstrate that coalescent samplers hold great promise for detecting weak but meaningful population structure, and defining appropriate management units. John Wiley and Sons Inc. 2018-10-15 /pmc/articles/PMC6346657/ /pubmed/30697337 http://dx.doi.org/10.1111/eva.12712 Text en © 2018 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Crandall, Eric D.
Toonen, Robert J.
Selkoe, Kimberly A.
A coalescent sampler successfully detects biologically meaningful population structure overlooked by F‐statistics
title A coalescent sampler successfully detects biologically meaningful population structure overlooked by F‐statistics
title_full A coalescent sampler successfully detects biologically meaningful population structure overlooked by F‐statistics
title_fullStr A coalescent sampler successfully detects biologically meaningful population structure overlooked by F‐statistics
title_full_unstemmed A coalescent sampler successfully detects biologically meaningful population structure overlooked by F‐statistics
title_short A coalescent sampler successfully detects biologically meaningful population structure overlooked by F‐statistics
title_sort coalescent sampler successfully detects biologically meaningful population structure overlooked by f‐statistics
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346657/
https://www.ncbi.nlm.nih.gov/pubmed/30697337
http://dx.doi.org/10.1111/eva.12712
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