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. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2647-399da7d841fd39e8e2de8d00ce3e321bc0d1241f696a48638fbc220d53222d183</citedby><cites>FETCH-LOGICAL-c2647-399da7d841fd39e8e2de8d00ce3e321bc0d1241f696a48638fbc220d53222d183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0049837&type=printable$$EPDF$$P50$$Gplos$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0049837$$EHTML$$P50$$Gplos$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,864,2928,23866,27344,27924,27925,33774,79600,79601</link.rule.ids></links><search><contributor>Mailund, Thomas</contributor><creatorcontrib>Elhaik, Eran</creatorcontrib><title>Empirical Distributions of FST from Large-Scale Human Polymorphism Data</title><title>PloS one</title><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.</description><subject>Adaptation</subject><subject>Alleles</subject><subject>Candidates</subject><subject>Chromosomes</subject><subject>Data processing</subject><subject>Demography</subject><subject>Differentiation</subject><subject>Empirical analysis</subject><subject>Gene frequency</subject><subject>Gene loci</subject><subject>Gene polymorphism</subject><subject>Genetic diversity</subject><subject>Genetics</subject><subject>Genomes</subject><subject>Linkage disequilibrium</subject><subject>Migration</subject><subject>Monte Carlo simulation</subject><subject>Natural selection</subject><subject>Polymorphism</subject><subject>Population</subject><subject>Population differentiation</subject><subject>Population genetics</subject><subject>Population growth</subject><subject>Population studies</subject><subject>Populations</subject><subject>Probability distribution functions</subject><subject>Race 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Distributions of FST from Large-Scale Human Polymorphism Data</title><author>Elhaik, Eran</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2647-399da7d841fd39e8e2de8d00ce3e321bc0d1241f696a48638fbc220d53222d183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adaptation</topic><topic>Alleles</topic><topic>Candidates</topic><topic>Chromosomes</topic><topic>Data processing</topic><topic>Demography</topic><topic>Differentiation</topic><topic>Empirical analysis</topic><topic>Gene frequency</topic><topic>Gene loci</topic><topic>Gene polymorphism</topic><topic>Genetic diversity</topic><topic>Genetics</topic><topic>Genomes</topic><topic>Linkage disequilibrium</topic><topic>Migration</topic><topic>Monte Carlo simulation</topic><topic>Natural selection</topic><topic>Polymorphism</topic><topic>Population</topic><topic>Population differentiation</topic><topic>Population 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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. 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.</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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