Genetics in geographically structured populations: defining, estimating and interpreting FST

Key Points Wright's F -statistics, and especially F ST , provide important insights into the evolutionary processes that influence the structure of genetic variation within and among populations, and they are among the most widely used descriptive statistics in population and evolutionary genet...

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Published inNature reviews. Genetics Vol. 10; no. 9; pp. 639 - 650
Main Authors Holsinger, Kent E., Weir, Bruce S.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.09.2009
Nature Publishing Group
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Abstract Key Points Wright's F -statistics, and especially F ST , provide important insights into the evolutionary processes that influence the structure of genetic variation within and among populations, and they are among the most widely used descriptive statistics in population and evolutionary genetics. F ST is a property of the distribution of allele frequencies among populations. It reflects the joint effects of drift, migration, mutation and selection on the distribution of genetic variation among populations. F ST has a central role in population and evolutionary genetics and has wide applications in fields from disease association mapping to forensic science. F ST can be used to describe the distribution of genetic variation among any set of samples, but it is most usefully applied when the samples represent discrete units rather than arbitrary divisions along a continuous distribution. Statistics related to F ST can be useful for haplotype or microsatellite data if an appropriate measure of evolutionary distance among alleles is available. Comparison of an estimate of F ST from marker data with an estimate of Q ST from continuously varying trait data can be used to detect selection, but the estimate of F ST may depend on the choice of marker and the estimate of Q ST may differ from neutral expectations if there is a non-additive component of genetic variance. Although the simple relationship between F ST and migration rates in Wright's island model makes it tempting to infer migration rates from F ST , caution is needed if such an approach is to be used. If estimates of F ST from many loci are available, it may be possible to identify certain loci as 'outliers' that may have been subject to different patterns of selection or to different demographic processes. Case–control studies for association-mapping studies must account for the possibility that population substructure accounts for an observed association between a marker and a disease. The genomic control method uses background estimates of F ST to control for such substructure. In forensic applications, the probabilities of obtaining a match are sometimes calculated for subpopulations that lack specific allele frequency data. A θ correction, in which θ is F ST , is used to calculate the probability of a match using allele frequency information from a broader population that the subpopulation is part of. The massive amount of data that is being generated by population genomics projects can be understood fundamentally as allelic variation at individual loci. We therefore expect F -statistics to be at least as useful in understanding these data sets as they have been in population and evolutionary genetics for most of the last century. F ST describes the processes that lead to genetic differentiation among and within populations and is widely used in population and evolutionary genetics. This article describes the meaning of F ST and how it should be estimated and interpreted. Wright's F -statistics, and especially F ST , provide important insights into the evolutionary processes that influence the structure of genetic variation within and among populations, and they are among the most widely used descriptive statistics in population and evolutionary genetics. Estimates of F ST can identify regions of the genome that have been the target of selection, and comparisons of F ST from different parts of the genome can provide insights into the demographic history of populations. For these reasons and others, F ST has a central role in population and evolutionary genetics and has wide applications in fields that range from disease association mapping to forensic science. This Review clarifies how F ST is defined, how it should be estimated, how it is related to similar statistics and how estimates of F ST should be interpreted.
AbstractList Wright's F-statistics, and especially F(ST), provide important insights into the evolutionary processes that influence the structure of genetic variation within and among populations, and they are among the most widely used descriptive statistics in population and evolutionary genetics. Estimates of F(ST) can identify regions of the genome that have been the target of selection, and comparisons of F(ST) from different parts of the genome can provide insights into the demographic history of populations. For these reasons and others, F(ST) has a central role in population and evolutionary genetics and has wide applications in fields that range from disease association mapping to forensic science. This Review clarifies how F(ST) is defined, how it should be estimated, how it is related to similar statistics and how estimates of F(ST) should be interpreted.
Key Points Wright's F -statistics, and especially F ST , provide important insights into the evolutionary processes that influence the structure of genetic variation within and among populations, and they are among the most widely used descriptive statistics in population and evolutionary genetics. F ST is a property of the distribution of allele frequencies among populations. It reflects the joint effects of drift, migration, mutation and selection on the distribution of genetic variation among populations. F ST has a central role in population and evolutionary genetics and has wide applications in fields from disease association mapping to forensic science. F ST can be used to describe the distribution of genetic variation among any set of samples, but it is most usefully applied when the samples represent discrete units rather than arbitrary divisions along a continuous distribution. Statistics related to F ST can be useful for haplotype or microsatellite data if an appropriate measure of evolutionary distance among alleles is available. Comparison of an estimate of F ST from marker data with an estimate of Q ST from continuously varying trait data can be used to detect selection, but the estimate of F ST may depend on the choice of marker and the estimate of Q ST may differ from neutral expectations if there is a non-additive component of genetic variance. Although the simple relationship between F ST and migration rates in Wright's island model makes it tempting to infer migration rates from F ST , caution is needed if such an approach is to be used. If estimates of F ST from many loci are available, it may be possible to identify certain loci as 'outliers' that may have been subject to different patterns of selection or to different demographic processes. Case–control studies for association-mapping studies must account for the possibility that population substructure accounts for an observed association between a marker and a disease. The genomic control method uses background estimates of F ST to control for such substructure. In forensic applications, the probabilities of obtaining a match are sometimes calculated for subpopulations that lack specific allele frequency data. A θ correction, in which θ is F ST , is used to calculate the probability of a match using allele frequency information from a broader population that the subpopulation is part of. The massive amount of data that is being generated by population genomics projects can be understood fundamentally as allelic variation at individual loci. We therefore expect F -statistics to be at least as useful in understanding these data sets as they have been in population and evolutionary genetics for most of the last century. F ST describes the processes that lead to genetic differentiation among and within populations and is widely used in population and evolutionary genetics. This article describes the meaning of F ST and how it should be estimated and interpreted. Wright's F -statistics, and especially F ST , provide important insights into the evolutionary processes that influence the structure of genetic variation within and among populations, and they are among the most widely used descriptive statistics in population and evolutionary genetics. Estimates of F ST can identify regions of the genome that have been the target of selection, and comparisons of F ST from different parts of the genome can provide insights into the demographic history of populations. For these reasons and others, F ST has a central role in population and evolutionary genetics and has wide applications in fields that range from disease association mapping to forensic science. This Review clarifies how F ST is defined, how it should be estimated, how it is related to similar statistics and how estimates of F ST should be interpreted.
Wright’s F -statistics, and especially F ST , provide important insights into the evolutionary processes that influence the structure of genetic variation within and among populations, and they are among the most widely used descriptive statistics in population and evolutionary genetics. Estimates of F ST can identify regions of the genome that have been the target of selection, and comparisons of F ST from different parts of the genome can provide insights into the demographic history of populations. For these reasons and others, F ST has a central role in population and evolutionary genetics and has wide applications in fields that range from disease association mapping to forensic science. This Review clarifies how F ST is defined, how it should be estimated, how it is related to similar statistics and how estimates of F ST should be interpreted.
Author Weir, Bruce S.
Holsinger, Kent E.
AuthorAffiliation Department of Ecology and Evolutionary Biology, U-3043, University of Connecticut, Storrs, Connecticut 06269-3043, USA
Department of Biostatistics, University of Washington, Box 357232, Seattle, Washington 98195, USA
AuthorAffiliation_xml – name: Department of Ecology and Evolutionary Biology, U-3043, University of Connecticut, Storrs, Connecticut 06269-3043, USA
– name: Department of Biostatistics, University of Washington, Box 357232, Seattle, Washington 98195, USA
Author_xml – sequence: 1
  givenname: Kent E.
  surname: Holsinger
  fullname: Holsinger, Kent E.
  email: kent@darwin.eeb.uconn.edu
  organization: Department of Ecology and Evolutionary Biology, U-3043, University of Connecticut
– sequence: 2
  givenname: Bruce S.
  surname: Weir
  fullname: Weir, Bruce S.
  email: bsweir@u.washington.edu
  organization: Department of Biostatistics, University of Washington, Box 357232
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Issue 9
Keywords Genetics
Review
Language English
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  year: 2009
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PublicationTitle Nature reviews. Genetics
PublicationTitleAbbrev Nat Rev Genet
PublicationYear 2009
Publisher Nature Publishing Group UK
Nature Publishing Group
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Snippet Key Points Wright's F -statistics, and especially F ST , provide important insights into the evolutionary processes that influence the structure of genetic...
Wright's F-statistics, and especially F(ST), provide important insights into the evolutionary processes that influence the structure of genetic variation...
Wright’s F -statistics, and especially F ST , provide important insights into the evolutionary processes that influence the structure of genetic variation...
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SubjectTerms Agriculture
Animal Genetics and Genomics
Biological and medical sciences
Biomedical and Life Sciences
Biomedicine
Cancer Research
Estimates
Forensic sciences
Fundamental and applied biological sciences. Psychology
Gene Function
Genetic diversity
Genetics of eukaryotes. Biological and molecular evolution
Genomes
Human Genetics
Migration
Population
review-article
Statistics
Title Genetics in geographically structured populations: defining, estimating and interpreting FST
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https://www.proquest.com/docview/223749851
https://pubmed.ncbi.nlm.nih.gov/PMC4687486
Volume 10
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