Literature DB >> 11704929

The discovery of single-nucleotide polymorphisms--and inferences about human demographic history.

J Wakeley1, R Nielsen, S N Liu-Cordero, K Ardlie.   

Abstract

A method of historical inference that accounts for ascertainment bias is developed and applied to single-nucleotide polymorphism (SNP) data in humans. The data consist of 84 short fragments of the genome that were selected, from three recent SNP surveys, to contain at least two polymorphisms in their respective ascertainment samples and that were then fully resequenced in 47 globally distributed individuals. Ascertainment bias is the deviation, from what would be observed in a random sample, caused either by discovery of polymorphisms in small samples or by locus selection based on levels or patterns of polymorphism. The three SNP surveys from which the present data were derived differ both in their protocols for ascertainment and in the size of the samples used for discovery. We implemented a Monte Carlo maximum-likelihood method to fit a subdivided-population model that includes a possible change in effective size at some time in the past. Incorrectly assuming that ascertainment bias does not exist causes errors in inference, affecting both estimates of migration rates and historical changes in size. Migration rates are overestimated when ascertainment bias is ignored. However, the direction of error in inferences about changes in effective population size (whether the population is inferred to be shrinking or growing) depends on whether either the numbers of SNPs per fragment or the SNP-allele frequencies are analyzed. We use the abbreviation "SDL," for "SNP-discovered locus," in recognition of the genomic-discovery context of SNPs. When ascertainment bias is modeled fully, both the number of SNPs per SDL and their allele frequencies support a scenario of growth in effective size in the context of a subdivided population. If subdivision is ignored, however, the hypothesis of constant effective population size cannot be rejected. An important conclusion of this work is that, in demographic or other studies, SNP data are useful only to the extent that their ascertainment can be modeled.

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Year:  2001        PMID: 11704929      PMCID: PMC1235544          DOI: 10.1086/324521

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  39 in total

1.  Estimation of population parameters and recombination rates from single nucleotide polymorphisms.

Authors:  R Nielsen
Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

2.  Haplotype variation and linkage disequilibrium in 313 human genes.

Authors:  J C Stephens; J A Schneider; D A Tanguay; J Choi; T Acharya; S E Stanley; R Jiang; C J Messer; A Chew; J H Han; J Duan; J L Carr; M S Lee; B Koshy; A M Kumar; G Zhang; W R Newell; A Windemuth; C Xu; T S Kalbfleisch; S L Shaner; K Arnold; V Schulz; C M Drysdale; K Nandabalan; R S Judson; G Ruano; G F Vovis
Journal:  Science       Date:  2001-07-12       Impact factor: 47.728

3.  Usefulness of single nucleotide polymorphism data for estimating population parameters.

Authors:  M K Kuhner; P Beerli; J Yamato; J Felsenstein
Journal:  Genetics       Date:  2000-09       Impact factor: 4.562

4.  On the number of segregating sites in genetical models without recombination.

Authors:  G A Watterson
Journal:  Theor Popul Biol       Date:  1975-04       Impact factor: 1.570

5.  Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1.

Authors:  N Yu; Z Zhao; Y X Fu; N Sambuughin; M Ramsay; T Jenkins; E Leskinen; L Patthy; L B Jorde; T Kuromori; W H Li
Journal:  Mol Biol Evol       Date:  2001-02       Impact factor: 16.240

6.  Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.

Authors:  F Tajima
Journal:  Genetics       Date:  1989-11       Impact factor: 4.562

7.  RFLP analysis on a sample from northern Italy.

Authors:  G Matullo; R M Griffo; J L Mountain; A Piazza; L L Cavalli-Sforza
Journal:  Gene Geogr       Date:  1994-04

8.  Statistical tests of neutrality of mutations.

Authors:  Y X Fu; W H Li
Journal:  Genetics       Date:  1993-03       Impact factor: 4.562

9.  Mitochondrial DNA and human evolution.

Authors:  R L Cann; M Stoneking; A C Wilson
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10.  Extensive nuclear DNA sequence diversity among chimpanzees.

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  51 in total

1.  SNPSTRs: empirically derived, rapidly typed, autosomal haplotypes for inference of population history and mutational processes.

Authors:  Joanna L Mountain; Alec Knight; Matthew Jobin; Christopher Gignoux; Adam Miller; Alice A Lin; Peter A Underhill
Journal:  Genome Res       Date:  2002-11       Impact factor: 9.043

2.  Interrogating a high-density SNP map for signatures of natural selection.

Authors:  Joshua M Akey; Ge Zhang; Kun Zhang; Li Jin; Mark D Shriver
Journal:  Genome Res       Date:  2002-12       Impact factor: 9.043

3.  A genealogical interpretation of linkage disequilibrium.

Authors:  Gilean A T McVean
Journal:  Genetics       Date:  2002-10       Impact factor: 4.562

4.  New explicit expressions for relative frequencies of single-nucleotide polymorphisms with application to statistical inference on population growth.

Authors:  A Polanski; M Kimmel
Journal:  Genetics       Date:  2003-09       Impact factor: 4.562

5.  Reconstituting the frequency spectrum of ascertained single-nucleotide polymorphism data.

Authors:  Rasmus Nielsen; Melissa J Hubisz; Andrew G Clark
Journal:  Genetics       Date:  2004-09-15       Impact factor: 4.562

6.  Ascertainment biases in SNP chips affect measures of population divergence.

Authors:  Anders Albrechtsen; Finn Cilius Nielsen; Rasmus Nielsen
Journal:  Mol Biol Evol       Date:  2010-06-17       Impact factor: 16.240

7.  Multi-locus inference of population structure: a comparison between single nucleotide polymorphisms and microsatellites.

Authors:  R J Haasl; B A Payseur
Journal:  Heredity (Edinb)       Date:  2010-03-24       Impact factor: 3.821

8.  Maximum-likelihood estimation of demographic parameters using the frequency spectrum of unlinked single-nucleotide polymorphisms.

Authors:  Alison M Adams; Richard R Hudson
Journal:  Genetics       Date:  2004-11       Impact factor: 4.562

9.  Calibrating a coalescent simulation of human genome sequence variation.

Authors:  Stephen F Schaffner; Catherine Foo; Stacey Gabriel; David Reich; Mark J Daly; David Altshuler
Journal:  Genome Res       Date:  2005-11       Impact factor: 9.043

10.  Assessment of Population Structure and Its Effects on Genome-Wide Association Studies.

Authors:  Hongyan Xu; Varghese George
Journal:  Commun Stat Theory Methods       Date:  2009-01-01       Impact factor: 0.893

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