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Comparison of Genome-Wide Association Methods in Analyses of Admixed Populations with Complex Familial Relationships
Population structure is known to cause false-positive detection in association studies. We compared the power, precision, and type-I error rates of various association models in analyses of a simulated dataset with structure at the population (admixture from two populations; P) and family (K) levels...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963841/ https://www.ncbi.nlm.nih.gov/pubmed/24662750 http://dx.doi.org/10.1371/journal.pone.0088926 |
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author | Kadri, Naveen K. Guldbrandtsen, Bernt Sørensen, Peter Sahana, Goutam |
author_facet | Kadri, Naveen K. Guldbrandtsen, Bernt Sørensen, Peter Sahana, Goutam |
author_sort | Kadri, Naveen K. |
collection | PubMed |
description | Population structure is known to cause false-positive detection in association studies. We compared the power, precision, and type-I error rates of various association models in analyses of a simulated dataset with structure at the population (admixture from two populations; P) and family (K) levels. We also compared type-I error rates among models in analyses of publicly available human and dog datasets. The models corrected for none, one, or both structure levels. Correction for K was performed with linear mixed models incorporating familial relationships estimated from pedigrees or genetic markers. Linear models that ignored K were also tested. Correction for P was performed using principal component or structured association analysis. In analyses of simulated and real data, linear mixed models that corrected for K were able to control for type-I error, regardless of whether they also corrected for P. In contrast, correction for P alone in linear models was insufficient. The power and precision of linear mixed models with and without correction for P were similar. Furthermore, power, precision, and type-I error rate were comparable in linear mixed models incorporating pedigree and genomic relationships. In summary, in association studies using samples with both P and K, ancestries estimated using principal components or structured assignment were not sufficient to correct type-I errors. In such cases type-I errors may be controlled by use of linear mixed models with relationships derived from either pedigree or from genetic markers. |
format | Online Article Text |
id | pubmed-3963841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39638412014-03-27 Comparison of Genome-Wide Association Methods in Analyses of Admixed Populations with Complex Familial Relationships Kadri, Naveen K. Guldbrandtsen, Bernt Sørensen, Peter Sahana, Goutam PLoS One Research Article Population structure is known to cause false-positive detection in association studies. We compared the power, precision, and type-I error rates of various association models in analyses of a simulated dataset with structure at the population (admixture from two populations; P) and family (K) levels. We also compared type-I error rates among models in analyses of publicly available human and dog datasets. The models corrected for none, one, or both structure levels. Correction for K was performed with linear mixed models incorporating familial relationships estimated from pedigrees or genetic markers. Linear models that ignored K were also tested. Correction for P was performed using principal component or structured association analysis. In analyses of simulated and real data, linear mixed models that corrected for K were able to control for type-I error, regardless of whether they also corrected for P. In contrast, correction for P alone in linear models was insufficient. The power and precision of linear mixed models with and without correction for P were similar. Furthermore, power, precision, and type-I error rate were comparable in linear mixed models incorporating pedigree and genomic relationships. In summary, in association studies using samples with both P and K, ancestries estimated using principal components or structured assignment were not sufficient to correct type-I errors. In such cases type-I errors may be controlled by use of linear mixed models with relationships derived from either pedigree or from genetic markers. Public Library of Science 2014-03-24 /pmc/articles/PMC3963841/ /pubmed/24662750 http://dx.doi.org/10.1371/journal.pone.0088926 Text en © 2014 Kadri et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kadri, Naveen K. Guldbrandtsen, Bernt Sørensen, Peter Sahana, Goutam Comparison of Genome-Wide Association Methods in Analyses of Admixed Populations with Complex Familial Relationships |
title | Comparison of Genome-Wide Association Methods in Analyses of Admixed Populations with Complex Familial Relationships |
title_full | Comparison of Genome-Wide Association Methods in Analyses of Admixed Populations with Complex Familial Relationships |
title_fullStr | Comparison of Genome-Wide Association Methods in Analyses of Admixed Populations with Complex Familial Relationships |
title_full_unstemmed | Comparison of Genome-Wide Association Methods in Analyses of Admixed Populations with Complex Familial Relationships |
title_short | Comparison of Genome-Wide Association Methods in Analyses of Admixed Populations with Complex Familial Relationships |
title_sort | comparison of genome-wide association methods in analyses of admixed populations with complex familial relationships |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963841/ https://www.ncbi.nlm.nih.gov/pubmed/24662750 http://dx.doi.org/10.1371/journal.pone.0088926 |
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