Assessing population differentiation and isolation from single-nucleotide polymorphism data

We introduce a new, hierarchical, model for single-nucleotide polymorphism allele frequencies in a structured population, which is naturally fitted via Markov chain Monte Carlo methods. There is one parameter for each population, closely analogous to a population-specific version of Wright's FS...

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Vydáno v:Journal of the Royal Statistical Society. Series B, Statistical methodology Ročník 64; číslo 4; s. 695 - 715
Hlavní autoři: Nicholson, George, Smith, Albert V., Jónsson, Frosti, Gústafsson, Ómar, Stefánsson, Kári, Donnelly, Peter
Médium: Journal Article
Jazyk:angličtina
Vydáno: Oxford, UK Blackwell Publishers 01.10.2002
Blackwell
Royal Statistical Society
Edice:Journal of the Royal Statistical Society Series B
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ISSN:1369-7412, 1467-9868
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Abstract We introduce a new, hierarchical, model for single-nucleotide polymorphism allele frequencies in a structured population, which is naturally fitted via Markov chain Monte Carlo methods. There is one parameter for each population, closely analogous to a population-specific version of Wright's FST, which can be interpreted as measuring how isolated the relevant population has been. Our model includes the effects of single-nucleotide polymorphism ascertainment and is motivated by population genetics considerations, explicitly in the transient setting after divergence of populations, rather than as the equilibrium of a stochastic model, as is traditionally the case. For the sizes of data set that we consider the method provides good parameter estimates and considerably outperforms estimation methods analogous to those currently used in practice. We apply the method to one new and one existing human data set, each with rather different characteristics-the first consisting of three rather close European populations; the second of four populations taken from across the globe. A novelty of our framework is that the fit of the underlying model can be assessed easily, and these results are encouraging for both data sets analysed. Our analysis suggests that Iceland is more differentiated than the other two European populations (France and Utah), a finding which is consistent with the historical record, but not obvious from comparisons of simple summary statistics.
AbstractList We introduce a new, hierarchical, model for single-nucleotide polymorphism allele frequencies in a structured population, which is naturally fitted via Markov chain Monte Carlo methods. There is one parameter for each population, closely analogous to a population-specific version of Wright's FST, which can be interpreted as measuring how isolated the relevant population has been. Our model includes the effects of single-nucleotide polymorphism ascertainment and is motivated by population genetics considerations, explicitly in the transient setting after divergence of populations, rather than as the equilibrium of a stochastic model, as is traditionally the case. For the sizes of data set that we consider the method provides good parameter estimates and considerably outperforms estimation methods analogous to those currently used in practice. We apply the method to one new and one existing human data set, each with rather different characteristics—the first consisting of three rather close European populations; the second of four populations taken from across the globe. A novelty of our framework is that the fit of the underlying model can be assessed easily, and these results are encouraging for both data sets analysed. Our analysis suggests that Iceland is more differentiated than the other two European populations (France and Utah), a finding which is consistent with the historical record, but not obvious from comparisons of simple summary statistics.
We introduce a new, hierarchical, model for single-nucleotide polymorphism allele frequencies in a structured population, which is naturally fitted via Markov chain Monte Carlo methods. There is one parameter for each population, closely analogous to a population-specific version of Wright's "F""ST", which can be interpreted as measuring how isolated the relevant population has been. Our model includes the effects of single-nucleotide polymorphism ascertainment and is motivated by population genetics considerations, explicitly in the transient setting after divergence of populations, rather than as the equilibrium of a stochastic model, as is traditionally the case. For the sizes of data set that we consider the method provides good parameter estimates and considerably outperforms estimation methods analogous to those currently used in practice. We apply the method to one new and one existing human data set, each with rather different characteristics-the first consisting of three rather close European populations; the second of four populations taken from across the globe. A novelty of our framework is that the fit of the underlying model can be assessed easily, and these results are encouraging for both data sets analysed. Our analysis suggests that Iceland is more differentiated than the other two European populations (France and Utah), a finding which is consistent with the historical record, but not obvious from comparisons of simple summary statistics. Copyright 2002 Royal Statistical Society.
Author Gústafsson, Ómar
Stefánsson, Kári
Nicholson, George
Donnelly, Peter
Smith, Albert V.
Jónsson, Frosti
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  givenname: Albert V.
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  surname: Jónsson
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  surname: Stefánsson
  fullname: Stefánsson, Kári
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  givenname: Peter
  surname: Donnelly
  fullname: Donnelly, Peter
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Issue 4
Keywords Human
Bottleneck
Stochastic model
Monte Carlo method
Parameter estimation
Demography
Index
History
Population genetics
Markov chain
Statistical method
Fixation
Wright Fisher diffusion
Genetics
Hierarchical model
Population dynamics
Diffusion
Differentiation
Fixation index
Population history
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Royal Statistical Society
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References_xml – reference: Bowcock, A., Hebert, J., Mountain, J., Kidd, J., Rogers, J., Kidd, K. and Cavalli-Sforza, L. (1991a) Study of an additional 58 dna markers in five populations from four continents. Gene Geogr., 5, 151-173.
– reference: Roeder, K., Escobar, M., Kadane, J. and Balazs, I. (1998) Measuring heterogeneity in forensic databases using hierarchical Bayes models. Biometrika, 85, 269-287.
– reference: - (1982) The shifting balances theory and macroevolution. A. Rev. Genet., 16, 1-19.
– reference: Wakeley, J. (2001) The coalescent in an island model of population subdivision with variation among demes. Theor. Popln Biol., 59, 133-144.
– reference: Wakeley, J., Nielsen, R., Liu-Cordero, S. and Ardlie, K. (2001) The discovery of single-nucleotide polymorphisms-and inferences about human demographic history. Am. J. Hum. Genet., 69, 1332-1347.
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Snippet We introduce a new, hierarchical, model for single-nucleotide polymorphism allele frequencies in a structured population, which is naturally fitted via Markov...
We introduce a new, hierarchical, model for single‐nucleotide polymorphism allele frequencies in a structured population, which is naturally fitted via Markov...
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SubjectTerms Bayes estimators
Biological and medical sciences
Bottleneck
Chromosomes
Coalescent
Datasets
Demography
Estimation
Estimators
Exact sciences and technology
Fixation indices
Forensic genetics
France
Fundamental and applied biological sciences. Psychology
Gene frequency
General aspects
Genetic loci
Human genetics
Iceland
Inference from stochastic processes; time series analysis
Markov chain Monte Carlo methods
Markov processes
Markovian processes
Mathematics
Mathematics in biology. Statistical analysis. Models. Metrology. Data processing in biology (general aspects)
Monte Carlo simulation
Population
Population genetics
Population histories
Population parameters
Probability and statistics
Probability theory and stochastic processes
Sciences and techniques of general use
Statistical methods
Statistical models
Statistics
Sufficiency and information
U.S.A
Utah
Title Assessing population differentiation and isolation from single-nucleotide polymorphism data
URI https://api.istex.fr/ark:/67375/WNG-DW0NR729-5/fulltext.pdf
https://www.jstor.org/stable/3088810
https://onlinelibrary.wiley.com/doi/abs/10.1111%2F1467-9868.00357
http://econpapers.repec.org/article/blajorssb/v_3a64_3ay_3a2002_3ai_3a4_3ap_3a695-715.htm
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