Your browser doesn't support javascript.
loading
Kernel machine methods for integrative analysis of genome-wide methylation and genotyping studies.
Zhao, Ni; Zhan, Xiang; Huang, Yen-Tsung; Almli, Lynn M; Smith, Alicia; Epstein, Michael P; Conneely, Karen; Wu, Michael C.
Afiliação
  • Zhao N; Department of Biostatistics, Johns Hopkins University, Baltimore, Maryland, 21205, United States of America.
  • Zhan X; Department of Public Health Sciences, Pennsylvania State University, Hershey, Pennsylvania, 17033, United States of America.
  • Huang YT; Institute of Statistical Science, Academia Sinica, Taipei, 11529, Taiwan.
  • Almli LM; Department of Psychiatry and Behavioral Sciences, Emory University, Atlanta, Georgia, 30322, United States of America.
  • Smith A; Department of Gynecology and Obstetrics, Emory University, Atlanta, Georgia, 30322, United States of America.
  • Epstein MP; Department of Human Genetics, Emory University, Atlanta, Georgia, 30322, United States of America.
  • Conneely K; Department of Human Genetics, Emory University, Atlanta, Georgia, 30322, United States of America.
  • Wu MC; Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, 98109, United States of America.
Genet Epidemiol ; 42(2): 156-167, 2018 03.
Article em En | MEDLINE | ID: mdl-29285792
ABSTRACT
Many large GWAS consortia are expanding to simultaneously examine the joint role of DNA methylation in addition to genotype in the same subjects. However, integrating information from both data types is challenging. In this paper, we propose a composite kernel machine regression model to test the joint epigenetic and genetic effect. Our approach works at the gene level, which allows for a common unit of analysis across different data types. The model compares the pairwise similarities in the phenotype to the pairwise similarities in the genotype and methylation values; and high correspondence is suggestive of association. A composite kernel is constructed to measure the similarities in the genotype and methylation values between pairs of samples. We demonstrate through simulations and real data applications that the proposed approach can correctly control type I error, and is more robust and powerful than using only the genotype or methylation data in detecting trait-associated genes. We applied our method to investigate the genetic and epigenetic regulation of gene expression in response to stressful life events using data that are collected from the Grady Trauma Project. Within the kernel machine testing framework, our methods allow for heterogeneity in effect sizes, nonlinear, and interactive effects, as well as rapid P-value computation.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metilação de DNA / Epigênese Genética / Estudo de Associação Genômica Ampla / Técnicas de Genotipagem Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metilação de DNA / Epigênese Genética / Estudo de Associação Genômica Ampla / Técnicas de Genotipagem Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article