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A general semi-parametric approach to the analysis of genetic association studies in population-based designs

BACKGROUND: For genetic association studies in designs of unrelated individuals, current statistical methodology typically models the phenotype of interest as a function of the genotype and assumes a known statistical model for the phenotype. In the analysis of complex phenotypes, especially in the...

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Autores principales: Lutz, Sharon, Yip, Wai-Ki, Hokanson, John, Laird, Nan, Lange, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648382/
https://www.ncbi.nlm.nih.gov/pubmed/23448186
http://dx.doi.org/10.1186/1471-2156-14-13
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author Lutz, Sharon
Yip, Wai-Ki
Hokanson, John
Laird, Nan
Lange, Christoph
author_facet Lutz, Sharon
Yip, Wai-Ki
Hokanson, John
Laird, Nan
Lange, Christoph
author_sort Lutz, Sharon
collection PubMed
description BACKGROUND: For genetic association studies in designs of unrelated individuals, current statistical methodology typically models the phenotype of interest as a function of the genotype and assumes a known statistical model for the phenotype. In the analysis of complex phenotypes, especially in the presence of ascertainment conditions, the specification of such model assumptions is not straight-forward and is error-prone, potentially causing misleading results. RESULTS: In this paper, we propose an alternative approach that treats the genotype as the random variable and conditions upon the phenotype. Thereby, the validity of the approach does not depend on the correctness of assumptions about the phenotypic model. Misspecification of the phenotypic model may lead to reduced statistical power. Theoretical derivations and simulation studies demonstrate both the validity and the advantages of the approach over existing methodology. In the COPDGene study (a GWAS for Chronic Obstructive Pulmonary Disease (COPD)), we apply the approach to a secondary, quantitative phenotype, the Fagerstrom nicotine dependence score, that is correlated with COPD affection status. The software package that implements this method is available. CONCLUSIONS: The flexibility of this approach enables the straight-forward application to quantitative phenotypes and binary traits in ascertained and unascertained samples. In addition to its robustness features, our method provides the platform for the construction of complex statistical models for longitudinal data, multivariate data, multi-marker tests, rare-variant analysis, and others.
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spelling pubmed-36483822013-05-10 A general semi-parametric approach to the analysis of genetic association studies in population-based designs Lutz, Sharon Yip, Wai-Ki Hokanson, John Laird, Nan Lange, Christoph BMC Genet Methodology Article BACKGROUND: For genetic association studies in designs of unrelated individuals, current statistical methodology typically models the phenotype of interest as a function of the genotype and assumes a known statistical model for the phenotype. In the analysis of complex phenotypes, especially in the presence of ascertainment conditions, the specification of such model assumptions is not straight-forward and is error-prone, potentially causing misleading results. RESULTS: In this paper, we propose an alternative approach that treats the genotype as the random variable and conditions upon the phenotype. Thereby, the validity of the approach does not depend on the correctness of assumptions about the phenotypic model. Misspecification of the phenotypic model may lead to reduced statistical power. Theoretical derivations and simulation studies demonstrate both the validity and the advantages of the approach over existing methodology. In the COPDGene study (a GWAS for Chronic Obstructive Pulmonary Disease (COPD)), we apply the approach to a secondary, quantitative phenotype, the Fagerstrom nicotine dependence score, that is correlated with COPD affection status. The software package that implements this method is available. CONCLUSIONS: The flexibility of this approach enables the straight-forward application to quantitative phenotypes and binary traits in ascertained and unascertained samples. In addition to its robustness features, our method provides the platform for the construction of complex statistical models for longitudinal data, multivariate data, multi-marker tests, rare-variant analysis, and others. BioMed Central 2013-02-28 /pmc/articles/PMC3648382/ /pubmed/23448186 http://dx.doi.org/10.1186/1471-2156-14-13 Text en Copyright © 2013 Lutz 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 Methodology Article
Lutz, Sharon
Yip, Wai-Ki
Hokanson, John
Laird, Nan
Lange, Christoph
A general semi-parametric approach to the analysis of genetic association studies in population-based designs
title A general semi-parametric approach to the analysis of genetic association studies in population-based designs
title_full A general semi-parametric approach to the analysis of genetic association studies in population-based designs
title_fullStr A general semi-parametric approach to the analysis of genetic association studies in population-based designs
title_full_unstemmed A general semi-parametric approach to the analysis of genetic association studies in population-based designs
title_short A general semi-parametric approach to the analysis of genetic association studies in population-based designs
title_sort general semi-parametric approach to the analysis of genetic association studies in population-based designs
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648382/
https://www.ncbi.nlm.nih.gov/pubmed/23448186
http://dx.doi.org/10.1186/1471-2156-14-13
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