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Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing.
Thornton, Timothy; Conomos, Matthew P; Sverdlov, Serge; Blue, Elizabeth M; Cheung, Charles Yk; Glazner, Christopher G; Lewis, Steven M; Wijsman, Ellen M.
Afiliação
  • Thornton T; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Conomos MP; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Sverdlov S; Department of Statistics, University of Washington, 313 Padelford Hall, Seattle, WA 98195, USA.
  • Blue EM; Department of Medicine, Division of Medical Genetics, University of Washington, Health Sciences Building, K-253, Box 357720, Seattle, WA 98195, USA.
  • Cheung CY; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Glazner CG; Department of Statistics, University of Washington, 313 Padelford Hall, Seattle, WA 98195, USA.
  • Lewis SM; Department of Statistics, University of Washington, 313 Padelford Hall, Seattle, WA 98195, USA.
  • Wijsman EM; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA ; Department of Medicine, Division of Medical Genetics, University of Washington, Health Sciences Building, K-253, Box 357720, Seattle, WA 98195, USA.
BMC Proc ; 8(Suppl 1): S5, 2014.
Article em En | MEDLINE | ID: mdl-25519330
It is well known that genetic association studies are not robust to population stratification. Two widely used approaches for the detection and correction of population structure are principal component analysis and model-based estimation of ancestry. These methods have been shown to give reliable inference on population structure in unrelated samples. We evaluated these two approaches in Mexican American pedigrees provided by the Genetic Analysis Workshop 18. We also estimated identity-by-descent sharing probabilities and kinship coefficients, with adjustment for ancestry admixture, to confirm documented pedigree relationships as well as to identify cryptic relatedness in the sample. We also estimated the heritability of the first simulated replicate of diastolic blood pressure (DBP). Finally, we performed an association analysis with simulated DBP, comparing the performance of an association method that corrects for population structure but does not account for relatedness to a method that adjusts for both population and pedigree structure. Analyses with simulated DBP were performed with knowledge of the underlying trait model.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: BMC Proc Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: BMC Proc Ano de publicação: 2014 Tipo de documento: Article