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Effects of population structure on genetic association studies

Population-based case-control association is a promising approach for unravelling the genetic basis of complex diseases. One potential problem of this approach is the presence of population structure in the samples. Using the Collaborative Study on the Genetics of Alcoholism (COGA) single-nucleotide...

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Detalles Bibliográficos
Autores principales: Xu, Hongyan, Shete, Sanjay
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866830/
https://www.ncbi.nlm.nih.gov/pubmed/16451565
http://dx.doi.org/10.1186/1471-2156-6-S1-S109
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author Xu, Hongyan
Shete, Sanjay
author_facet Xu, Hongyan
Shete, Sanjay
author_sort Xu, Hongyan
collection PubMed
description Population-based case-control association is a promising approach for unravelling the genetic basis of complex diseases. One potential problem of this approach is the presence of population structure in the samples. Using the Collaborative Study on the Genetics of Alcoholism (COGA) single-nucleotide polymorphism (SNP) datasets, we addressed three questions: How can the degree of population structure be quantified, and how does the population structure affect association studies? How accurate and efficient is the genomic control method in correcting for population structure? The amount of population structure in the COGA SNP data was found to inflate the p-value in association tests. Genomic control was found to be effective only when the appropriate number of markers was used in the control group in order to correctly calibrate the test. The approach presented in this paper could be used to select the appropriate number of markers for use in the genomic control method of correcting population structure.
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spelling pubmed-18668302007-05-11 Effects of population structure on genetic association studies Xu, Hongyan Shete, Sanjay BMC Genet Proceedings Population-based case-control association is a promising approach for unravelling the genetic basis of complex diseases. One potential problem of this approach is the presence of population structure in the samples. Using the Collaborative Study on the Genetics of Alcoholism (COGA) single-nucleotide polymorphism (SNP) datasets, we addressed three questions: How can the degree of population structure be quantified, and how does the population structure affect association studies? How accurate and efficient is the genomic control method in correcting for population structure? The amount of population structure in the COGA SNP data was found to inflate the p-value in association tests. Genomic control was found to be effective only when the appropriate number of markers was used in the control group in order to correctly calibrate the test. The approach presented in this paper could be used to select the appropriate number of markers for use in the genomic control method of correcting population structure. BioMed Central 2005-12-30 /pmc/articles/PMC1866830/ /pubmed/16451565 http://dx.doi.org/10.1186/1471-2156-6-S1-S109 Text en Copyright © 2005 Xu and Shete; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
Xu, Hongyan
Shete, Sanjay
Effects of population structure on genetic association studies
title Effects of population structure on genetic association studies
title_full Effects of population structure on genetic association studies
title_fullStr Effects of population structure on genetic association studies
title_full_unstemmed Effects of population structure on genetic association studies
title_short Effects of population structure on genetic association studies
title_sort effects of population structure on genetic association studies
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866830/
https://www.ncbi.nlm.nih.gov/pubmed/16451565
http://dx.doi.org/10.1186/1471-2156-6-S1-S109
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