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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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Detalles Bibliográficos
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
Descripción
Sumario: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.