Empirical Distributions of FST from Large-Scale Human Polymorphism Data

Studies of the apportionment of human genetic variation have long established that most human variation is within population groups and that the additional variation between population groups is small but greatest when comparing different continental populations. These studies often used Wright’s FS...

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description Studies of the apportionment of human genetic variation have long established that most human variation is within population groups and that the additional variation between population groups is small but greatest when comparing different continental populations. These studies often used Wright’s FST that apportions the standardized variance in allele frequencies within and between population groups. Because local adaptations increase population differentiation, high-FST may be found at closely linked loci under selection and used to identify genes undergoing directional or heterotic selection. We re-examined these processes using HapMap data. We analyzed 3 million SNPs on 602 samples from eight worldwide populations and a consensus subset of 1 million SNPs found in all populations. We identified four major features of the data: First, a hierarchically FST analysis showed that only a paucity (12%) of the total genetic variation is distributed between continental populations and even a lesser genetic variation (1%) is found between intra-continental populations. Second, the global FST distribution closely follows an exponential distribution. Third, although the overall FST distribution is similarly shaped (inverse J), FST distributions varies markedly by allele frequency when divided into non-overlapping groups by allele frequency range. Because the mean allele frequency is a crude indicator of allele age, these distributions mark the time-dependent change in genetic differentiation. Finally, the change in mean-FST of these groups is linear in allele frequency. These results suggest that investigating the extremes of the FST distribution for each allele frequency group is more efficient for detecting selection. Consequently, we demonstrate that such extreme SNPs are more clustered along the chromosomes than expected from linkage disequilibrium for each allele frequency group. These genomic regions are therefore likely candidates for natural selection.
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These studies often used Wright’s FST that apportions the standardized variance in allele frequencies within and between population groups. Because local adaptations increase population differentiation, high-FST may be found at closely linked loci under selection and used to identify genes undergoing directional or heterotic selection. We re-examined these processes using HapMap data. We analyzed 3 million SNPs on 602 samples from eight worldwide populations and a consensus subset of 1 million SNPs found in all populations. We identified four major features of the data: First, a hierarchically FST analysis showed that only a paucity (12%) of the total genetic variation is distributed between continental populations and even a lesser genetic variation (1%) is found between intra-continental populations. Second, the global FST distribution closely follows an exponential distribution. Third, although the overall FST distribution is similarly shaped (inverse J), FST distributions varies markedly by allele frequency when divided into non-overlapping groups by allele frequency range. Because the mean allele frequency is a crude indicator of allele age, these distributions mark the time-dependent change in genetic differentiation. Finally, the change in mean-FST of these groups is linear in allele frequency. These results suggest that investigating the extremes of the FST distribution for each allele frequency group is more efficient for detecting selection. Consequently, we demonstrate that such extreme SNPs are more clustered along the chromosomes than expected from linkage disequilibrium for each allele frequency group. These genomic regions are therefore likely candidates for natural selection.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0049837</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Adaptation ; Alleles ; Candidates ; Chromosomes ; Data processing ; Demography ; Differentiation ; Empirical analysis ; Gene frequency ; Gene loci ; Gene polymorphism ; Genetic diversity ; Genetics ; Genomes ; Linkage disequilibrium ; Migration ; Monte Carlo simulation ; Natural selection ; Polymorphism ; Population ; Population differentiation ; Population genetics ; Population growth ; Population studies ; Populations ; Probability distribution functions ; Race relations ; Single-nucleotide polymorphism ; Statistics ; Studies ; T cell receptors</subject><ispartof>PloS one, 2012-11, Vol.7 (11), p.e49837</ispartof><rights>2012 Eran Elhaik. 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Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Empirical Distributions of FST from Large-Scale Human Polymorphism Data</atitle><jtitle>PloS one</jtitle><date>2012-11-21</date><risdate>2012</risdate><volume>7</volume><issue>11</issue><spage>e49837</spage><pages>e49837-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Studies of the apportionment of human genetic variation have long established that most human variation is within population groups and that the additional variation between population groups is small but greatest when comparing different continental populations. 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Third, although the overall FST distribution is similarly shaped (inverse J), FST distributions varies markedly by allele frequency when divided into non-overlapping groups by allele frequency range. Because the mean allele frequency is a crude indicator of allele age, these distributions mark the time-dependent change in genetic differentiation. Finally, the change in mean-FST of these groups is linear in allele frequency. These results suggest that investigating the extremes of the FST distribution for each allele frequency group is more efficient for detecting selection. Consequently, we demonstrate that such extreme SNPs are more clustered along the chromosomes than expected from linkage disequilibrium for each allele frequency group. These genomic regions are therefore likely candidates for natural selection.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0049837</doi><oa>free_for_read</oa></addata></record>
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subjects Adaptation
Alleles
Candidates
Chromosomes
Data processing
Demography
Differentiation
Empirical analysis
Gene frequency
Gene loci
Gene polymorphism
Genetic diversity
Genetics
Genomes
Linkage disequilibrium
Migration
Monte Carlo simulation
Natural selection
Polymorphism
Population
Population differentiation
Population genetics
Population growth
Population studies
Populations
Probability distribution functions
Race relations
Single-nucleotide polymorphism
Statistics
Studies
T cell receptors
title Empirical Distributions of FST from Large-Scale Human Polymorphism Data
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