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Estimating the Effective Population Size from Temporal Allele Frequency Changes in Experimental Evolution

The effective population size ([Formula: see text]) is a major factor determining allele frequency changes in natural and experimental populations. Temporal methods provide a powerful and simple approach to estimate short-term [Formula: see text] They use allele frequency shifts between temporal sam...

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Autores principales: Jónás, Ágnes, Taus, Thomas, Kosiol, Carolin, Schlötterer, Christian, Futschik, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5068858/
https://www.ncbi.nlm.nih.gov/pubmed/27542959
http://dx.doi.org/10.1534/genetics.116.191197
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author Jónás, Ágnes
Taus, Thomas
Kosiol, Carolin
Schlötterer, Christian
Futschik, Andreas
author_facet Jónás, Ágnes
Taus, Thomas
Kosiol, Carolin
Schlötterer, Christian
Futschik, Andreas
author_sort Jónás, Ágnes
collection PubMed
description The effective population size ([Formula: see text]) is a major factor determining allele frequency changes in natural and experimental populations. Temporal methods provide a powerful and simple approach to estimate short-term [Formula: see text] They use allele frequency shifts between temporal samples to calculate the standardized variance, which is directly related to [Formula: see text] Here we focus on experimental evolution studies that often rely on repeated sequencing of samples in pools (Pool-seq). Pool-seq is cost-effective and often outperforms individual-based sequencing in estimating allele frequencies, but it is associated with atypical sampling properties: Additional to sampling individuals, sequencing DNA in pools leads to a second round of sampling, which increases the variance of allele frequency estimates. We propose a new estimator of [Formula: see text] which relies on allele frequency changes in temporal data and corrects for the variance in both sampling steps. In simulations, we obtain accurate [Formula: see text] estimates, as long as the drift variance is not too small compared to the sampling and sequencing variance. In addition to genome-wide [Formula: see text] estimates, we extend our method using a recursive partitioning approach to estimate [Formula: see text] locally along the chromosome. Since the type I error is controlled, our method permits the identification of genomic regions that differ significantly in their [Formula: see text] estimates. We present an application to Pool-seq data from experimental evolution with Drosophila and provide recommendations for whole-genome data. The estimator is computationally efficient and available as an R package at https://github.com/ThomasTaus/Nest.
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spelling pubmed-50688582016-10-21 Estimating the Effective Population Size from Temporal Allele Frequency Changes in Experimental Evolution Jónás, Ágnes Taus, Thomas Kosiol, Carolin Schlötterer, Christian Futschik, Andreas Genetics Investigations The effective population size ([Formula: see text]) is a major factor determining allele frequency changes in natural and experimental populations. Temporal methods provide a powerful and simple approach to estimate short-term [Formula: see text] They use allele frequency shifts between temporal samples to calculate the standardized variance, which is directly related to [Formula: see text] Here we focus on experimental evolution studies that often rely on repeated sequencing of samples in pools (Pool-seq). Pool-seq is cost-effective and often outperforms individual-based sequencing in estimating allele frequencies, but it is associated with atypical sampling properties: Additional to sampling individuals, sequencing DNA in pools leads to a second round of sampling, which increases the variance of allele frequency estimates. We propose a new estimator of [Formula: see text] which relies on allele frequency changes in temporal data and corrects for the variance in both sampling steps. In simulations, we obtain accurate [Formula: see text] estimates, as long as the drift variance is not too small compared to the sampling and sequencing variance. In addition to genome-wide [Formula: see text] estimates, we extend our method using a recursive partitioning approach to estimate [Formula: see text] locally along the chromosome. Since the type I error is controlled, our method permits the identification of genomic regions that differ significantly in their [Formula: see text] estimates. We present an application to Pool-seq data from experimental evolution with Drosophila and provide recommendations for whole-genome data. The estimator is computationally efficient and available as an R package at https://github.com/ThomasTaus/Nest. Genetics Society of America 2016-10 2016-08-19 /pmc/articles/PMC5068858/ /pubmed/27542959 http://dx.doi.org/10.1534/genetics.116.191197 Text en Copyright © 2016 Jónás et al. Available freely online through the author-supported open access option. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Jónás, Ágnes
Taus, Thomas
Kosiol, Carolin
Schlötterer, Christian
Futschik, Andreas
Estimating the Effective Population Size from Temporal Allele Frequency Changes in Experimental Evolution
title Estimating the Effective Population Size from Temporal Allele Frequency Changes in Experimental Evolution
title_full Estimating the Effective Population Size from Temporal Allele Frequency Changes in Experimental Evolution
title_fullStr Estimating the Effective Population Size from Temporal Allele Frequency Changes in Experimental Evolution
title_full_unstemmed Estimating the Effective Population Size from Temporal Allele Frequency Changes in Experimental Evolution
title_short Estimating the Effective Population Size from Temporal Allele Frequency Changes in Experimental Evolution
title_sort estimating the effective population size from temporal allele frequency changes in experimental evolution
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5068858/
https://www.ncbi.nlm.nih.gov/pubmed/27542959
http://dx.doi.org/10.1534/genetics.116.191197
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