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Clustering by genetic ancestry using genome-wide SNP data
BACKGROUND: Population stratification can cause spurious associations in a genome-wide association study (GWAS), and occurs when differences in allele frequencies of single nucleotide polymorphisms (SNPs) are due to ancestral differences between cases and controls rather than the trait of interest....
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018397/ https://www.ncbi.nlm.nih.gov/pubmed/21143920 http://dx.doi.org/10.1186/1471-2156-11-108 |
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author | Solovieff, Nadia Hartley, Stephen W Baldwin, Clinton T Perls, Thomas T Steinberg, Martin H Sebastiani, Paola |
author_facet | Solovieff, Nadia Hartley, Stephen W Baldwin, Clinton T Perls, Thomas T Steinberg, Martin H Sebastiani, Paola |
author_sort | Solovieff, Nadia |
collection | PubMed |
description | BACKGROUND: Population stratification can cause spurious associations in a genome-wide association study (GWAS), and occurs when differences in allele frequencies of single nucleotide polymorphisms (SNPs) are due to ancestral differences between cases and controls rather than the trait of interest. Principal components analysis (PCA) is the established approach to detect population substructure using genome-wide data and to adjust the genetic association for stratification by including the top principal components in the analysis. An alternative solution is genetic matching of cases and controls that requires, however, well defined population strata for appropriate selection of cases and controls. RESULTS: We developed a novel algorithm to cluster individuals into groups with similar ancestral backgrounds based on the principal components computed by PCA. We demonstrate the effectiveness of our algorithm in real and simulated data, and show that matching cases and controls using the clusters assigned by the algorithm substantially reduces population stratification bias. Through simulation we show that the power of our method is higher than adjustment for PCs in certain situations. CONCLUSIONS: In addition to reducing population stratification bias and improving power, matching creates a clean dataset free of population stratification which can then be used to build prediction models without including variables to adjust for ancestry. The cluster assignments also allow for the estimation of genetic heterogeneity by examining cluster specific effects. |
format | Text |
id | pubmed-3018397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30183972011-01-24 Clustering by genetic ancestry using genome-wide SNP data Solovieff, Nadia Hartley, Stephen W Baldwin, Clinton T Perls, Thomas T Steinberg, Martin H Sebastiani, Paola BMC Genet Methodology Article BACKGROUND: Population stratification can cause spurious associations in a genome-wide association study (GWAS), and occurs when differences in allele frequencies of single nucleotide polymorphisms (SNPs) are due to ancestral differences between cases and controls rather than the trait of interest. Principal components analysis (PCA) is the established approach to detect population substructure using genome-wide data and to adjust the genetic association for stratification by including the top principal components in the analysis. An alternative solution is genetic matching of cases and controls that requires, however, well defined population strata for appropriate selection of cases and controls. RESULTS: We developed a novel algorithm to cluster individuals into groups with similar ancestral backgrounds based on the principal components computed by PCA. We demonstrate the effectiveness of our algorithm in real and simulated data, and show that matching cases and controls using the clusters assigned by the algorithm substantially reduces population stratification bias. Through simulation we show that the power of our method is higher than adjustment for PCs in certain situations. CONCLUSIONS: In addition to reducing population stratification bias and improving power, matching creates a clean dataset free of population stratification which can then be used to build prediction models without including variables to adjust for ancestry. The cluster assignments also allow for the estimation of genetic heterogeneity by examining cluster specific effects. BioMed Central 2010-12-09 /pmc/articles/PMC3018397/ /pubmed/21143920 http://dx.doi.org/10.1186/1471-2156-11-108 Text en Copyright ©2010 Solovieff et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Solovieff, Nadia Hartley, Stephen W Baldwin, Clinton T Perls, Thomas T Steinberg, Martin H Sebastiani, Paola Clustering by genetic ancestry using genome-wide SNP data |
title | Clustering by genetic ancestry using genome-wide SNP data |
title_full | Clustering by genetic ancestry using genome-wide SNP data |
title_fullStr | Clustering by genetic ancestry using genome-wide SNP data |
title_full_unstemmed | Clustering by genetic ancestry using genome-wide SNP data |
title_short | Clustering by genetic ancestry using genome-wide SNP data |
title_sort | clustering by genetic ancestry using genome-wide snp data |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018397/ https://www.ncbi.nlm.nih.gov/pubmed/21143920 http://dx.doi.org/10.1186/1471-2156-11-108 |
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