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Testing for genetic association taking into account phenotypic information of relatives

We investigated efficient case-control association analysis using family data. The outcome of interest was coronary heart disease. We employed existing and new methods that take into account the correlations among related individuals to obtain the proper type I error rates. The methods considered fo...

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Detalles Bibliográficos
Autores principales: Uh, Hae-Won, Wijk, Henk Jan van der, Houwing-Duistermaat, Jeanine J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795896/
https://www.ncbi.nlm.nih.gov/pubmed/20017989
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author Uh, Hae-Won
Wijk, Henk Jan van der
Houwing-Duistermaat, Jeanine J
author_facet Uh, Hae-Won
Wijk, Henk Jan van der
Houwing-Duistermaat, Jeanine J
author_sort Uh, Hae-Won
collection PubMed
description We investigated efficient case-control association analysis using family data. The outcome of interest was coronary heart disease. We employed existing and new methods that take into account the correlations among related individuals to obtain the proper type I error rates. The methods considered for autosomal single-nucleotide polymorphisms were: 1) generalized estimating equations-based methods, 2) variance-modified Cochran-Armitage (MCA) trend test incorporating kinship coefficients, and 3) genotypic modified quasi-likelihood score test. Additionally, for X-linked single-nucleotide polymorphisms we proposed a two-degrees-of-freedom test. Performance of these methods was tested using Framingham Heart Study 500 k array data.
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spelling pubmed-27958962009-12-18 Testing for genetic association taking into account phenotypic information of relatives Uh, Hae-Won Wijk, Henk Jan van der Houwing-Duistermaat, Jeanine J BMC Proc Proceedings We investigated efficient case-control association analysis using family data. The outcome of interest was coronary heart disease. We employed existing and new methods that take into account the correlations among related individuals to obtain the proper type I error rates. The methods considered for autosomal single-nucleotide polymorphisms were: 1) generalized estimating equations-based methods, 2) variance-modified Cochran-Armitage (MCA) trend test incorporating kinship coefficients, and 3) genotypic modified quasi-likelihood score test. Additionally, for X-linked single-nucleotide polymorphisms we proposed a two-degrees-of-freedom test. Performance of these methods was tested using Framingham Heart Study 500 k array data. BioMed Central 2009-12-15 /pmc/articles/PMC2795896/ /pubmed/20017989 Text en Copyright ©2009 Uh et al; 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
Uh, Hae-Won
Wijk, Henk Jan van der
Houwing-Duistermaat, Jeanine J
Testing for genetic association taking into account phenotypic information of relatives
title Testing for genetic association taking into account phenotypic information of relatives
title_full Testing for genetic association taking into account phenotypic information of relatives
title_fullStr Testing for genetic association taking into account phenotypic information of relatives
title_full_unstemmed Testing for genetic association taking into account phenotypic information of relatives
title_short Testing for genetic association taking into account phenotypic information of relatives
title_sort testing for genetic association taking into account phenotypic information of relatives
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2795896/
https://www.ncbi.nlm.nih.gov/pubmed/20017989
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