Detecting Selection from Linked Sites Using an F-Model

被引:4
|
作者
Galimberti, Marco [1 ,2 ]
Leuenberger, Christoph [3 ]
Wolf, Beat [4 ]
Szilagyi, Sandor Miklos [5 ]
Foll, Matthieu [6 ]
Wegmann, Daniel [1 ,2 ]
机构
[1] Univ Fribourg, Dept Biol, Chemin Musee 10, CH-1700 Fribourg, Switzerland
[2] Univ Fribourg, Dept Math, CH-1700 Fribourg, Switzerland
[3] Swiss Inst Bioinformat, CH-1700 Fribourg, Switzerland
[4] Univ Appl Sci Western Switzerland, iCoSys, CH-1700 Switzerland, Switzerland
[5] Univ Med Pharm Sci & Technol Targu Mures, Dept Informat, Targu Mures 540139, Romania
[6] Int Agcy Res Canc IARC WHO, Sect Genet, F-69372 Lyon, France
基金
瑞士国家科学基金会;
关键词
Bayesian statistics; F-statistics; hidden Markov model; divergent selection; balancing selection; RECENT POSITIVE SELECTION; POPULATION-STRUCTURE; LACTASE-PERSISTENCE; GENOMIC REGIONS; MARKOV MODEL; GENE FLOW; LOCI; ADAPTATION; DIVERGENCE; SPECIATION;
D O I
10.1534/genetics.120.303780
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Allele frequencies vary across populations and loci, even in the presence of migration. While most differences may be due to genetic drift, divergent selection will further increase differentiation at some loci. Identifying those is key in studying local adaptation, but remains statistically challenging. A particularly elegant way to describe allele frequency differences among populations connected by migration is the F-model, which measures differences in allele frequencies by population specific F-ST coefficients. This model readily accounts for multiple evolutionary forces by partitioning F-ST coefficients into locus- and population-specific components reflecting selection and drift, respectively. Here we present an extension of this model to linked loci by means of a hidden Markov model (HMM), which characterizes the effect of selection on linked markers through correlations in the locus specific component along the genome. Using extensive simulations, we show that the statistical power of our method is up to twofold higher than that of previous implementations that assume sites to be independent. We finally evidence selection in the human genome by applying our method to data from the Human Genome Diversity Project (HGDP).
引用
收藏
页码:1205 / 1215
页数:11
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