2008
DOI: 10.1534/genetics.108.092221
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A Genome-Scan Method to Identify Selected Loci Appropriate for Both Dominant and Codominant Markers: A Bayesian Perspective

Abstract: Identifying loci under natural selection from genomic surveys is of great interest in different research areas. Commonly used methods to separate neutral effects from adaptive effects are based on locusspecific population differentiation coefficients to identify outliers. Here we extend such an approach to estimate directly the probability that each locus is subject to selection using a Bayesian method. We also extend it to allow the use of dominant markers like AFLPs. It has been shown that this model is robu… Show more

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Cited by 2,349 publications
(2,866 citation statements)
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References 39 publications
(78 reference statements)
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“…We used genotype by sequencing (GBS; Peterson et al., 2012) of two Illumina Hiseq libraries, de novo assembly into 90‐bp GBS tags with STACKS (Catchen, Amores, Hohenlohe, Cresko, & Postlethwait, 2011), latent factor mixed modeling [a genotype–environment association (GEA) method; Frichot, Schoville, Bouchard, & François, 2013], and two F ST outlier methods (Excoffier, Hofer, & Foll, 2009; Foll & Gaggiotti, 2008) to classify putatively neutral SNPS and SNPs exhibiting varying support for being under selection (Pais et al., 2016). Putatively neutral reference SNPs were used to calculate marker‐based inbreeding coefficients ( F ; Keller, Visscher, & Goddard, 2011) and identity‐by‐state matrices using PLINK (Purcell et al., 2007).…”
Section: Methodsmentioning
confidence: 99%
“…We used genotype by sequencing (GBS; Peterson et al., 2012) of two Illumina Hiseq libraries, de novo assembly into 90‐bp GBS tags with STACKS (Catchen, Amores, Hohenlohe, Cresko, & Postlethwait, 2011), latent factor mixed modeling [a genotype–environment association (GEA) method; Frichot, Schoville, Bouchard, & François, 2013], and two F ST outlier methods (Excoffier, Hofer, & Foll, 2009; Foll & Gaggiotti, 2008) to classify putatively neutral SNPS and SNPs exhibiting varying support for being under selection (Pais et al., 2016). Putatively neutral reference SNPs were used to calculate marker‐based inbreeding coefficients ( F ; Keller, Visscher, & Goddard, 2011) and identity‐by‐state matrices using PLINK (Purcell et al., 2007).…”
Section: Methodsmentioning
confidence: 99%
“…Methods of detecting F ST outliers resulting from “soft sweeps” suitable for low‐density SNP chip datasets include (i) FDIST2, which compares the F ST observed for a locus to the F ST expected under neutrality relative to its observed heterozygosity assuming an “n‐island” model where the effective population size of all population is constant as is the pairwise population migration rate (Antao, Lopes, Lopes, Beja‐Pereira, & Luikart, 2008; Beaumont & Nichols, 1996), (ii) Arlequin v.3.5, which implements FDIST2 methodology with the addition of a hierarchical island option that assumes two different constant migration rates with the lower rate among regional groups of populations and the higher rate among populations within the same region (Excoffier et al., 2009), and (iii) BayeScan, which separately estimates the posterior probability that each locus is under selection without assuming that all effective population sizes and migration rates are equal (Beaumont & Balding, 2004; Foll & Gaggiotti, 2008). In this study, Arlequin 3.5 and BayeScan 2.1 were chosen for the outlier analysis to be a good combination to reduce type I (false positive) and type II (false negative) error rates, which have been evaluated using simulation (Lotterhos & Whitlock, 2014; Narum & Hess, 2011; Vilas, Perez‐Figueroa, & Caballero, 2012).…”
Section: Methodsmentioning
confidence: 99%
“…BayeScan software V 2.1 (Foll & Gaggiotti, 2008) used a Bayesian approach via Markov Chain Monte Carlo (MCMC), assuming a prior Dirichlet distribution of alleles within populations and a hierarchical Bayesian model. The program calculates posterior odds, from the posterior probability of the models, with and without selection on a locus, using the proportion of loci with a strong increase in F ST relative to other loci among the MCMC outputs of its simulations (Beaumont & Balding, 2004).…”
Section: Methodsmentioning
confidence: 99%