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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...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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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. |
format | Text |
id | pubmed-2795896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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