The discovery of Single-Nucleotide Polymorphisms: and Inferences about Human Demographic History

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The discovery of Single-Nucleotide Polymorphisms : and Inferences about Human Demographic History. / Wakeley, John; Nielsen, Rasmus; Liu-Cordero, Shau Neen; Ardlie, Kristin.

In: American Journal of Human Genetics, Vol. 69, No. 6, 2001, p. 1332-1347.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Wakeley, J, Nielsen, R, Liu-Cordero, SN & Ardlie, K 2001, 'The discovery of Single-Nucleotide Polymorphisms: and Inferences about Human Demographic History', American Journal of Human Genetics, vol. 69, no. 6, pp. 1332-1347. https://doi.org/10.1086/324521

APA

Wakeley, J., Nielsen, R., Liu-Cordero, S. N., & Ardlie, K. (2001). The discovery of Single-Nucleotide Polymorphisms: and Inferences about Human Demographic History. American Journal of Human Genetics, 69(6), 1332-1347. https://doi.org/10.1086/324521

Vancouver

Wakeley J, Nielsen R, Liu-Cordero SN, Ardlie K. The discovery of Single-Nucleotide Polymorphisms: and Inferences about Human Demographic History. American Journal of Human Genetics. 2001;69(6):1332-1347. https://doi.org/10.1086/324521

Author

Wakeley, John ; Nielsen, Rasmus ; Liu-Cordero, Shau Neen ; Ardlie, Kristin. / The discovery of Single-Nucleotide Polymorphisms : and Inferences about Human Demographic History. In: American Journal of Human Genetics. 2001 ; Vol. 69, No. 6. pp. 1332-1347.

Bibtex

@article{397e2db07dfa4db2a11c0d4c91755a81,
title = "The discovery of Single-Nucleotide Polymorphisms: and Inferences about Human Demographic History",
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.",
author = "John Wakeley and Rasmus Nielsen and Liu-Cordero, {Shau Neen} and Kristin Ardlie",
year = "2001",
doi = "10.1086/324521",
language = "English",
volume = "69",
pages = "1332--1347",
journal = "American Journal of Human Genetics",
issn = "0002-9297",
publisher = "Cell Press",
number = "6",

}

RIS

TY - JOUR

T1 - The discovery of Single-Nucleotide Polymorphisms

T2 - and Inferences about Human Demographic History

AU - Wakeley, John

AU - Nielsen, Rasmus

AU - Liu-Cordero, Shau Neen

AU - Ardlie, Kristin

PY - 2001

Y1 - 2001

N2 - 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.

AB - 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.

U2 - 10.1086/324521

DO - 10.1086/324521

M3 - Journal article

C2 - 11704929

AN - SCOPUS:0035205317

VL - 69

SP - 1332

EP - 1347

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

IS - 6

ER -

ID: 222645092