| Literature DB >> 26478762 |
Jiahan Li1, Zhong Wang2, Runze Li3, Rongling Wu4.
Abstract
Although genome-wide association studies (GWAS) have proven powerful for comprehending the genetic architecture of complex traits, they are challenged by a high dimension of single-nucleotide polymorphisms (SNPs) as predictors, the presence of complex environmental factors, and longitudinal or functional natures of many complex traits or diseases. To address these challenges, we propose a high-dimensional varying-coefficient model for incorporating functional aspects of phenotypic traits into GWAS to formulate a so-called functional GWAS or fGWAS. Bayesian group lasso and the associated MCMC algorithms are developed to identify significant SNPs and estimate how they affect longitudinal traits through time-varying genetic actions. The model is generalized to analyze the genetic control of complex traits using subject-specific sparse longitudinal data. The statistical properties of the new model are investigated through simulation studies. We use the new model to analyze a real GWAS data set from the Framingham Heart Study, leading to the identification of several significant SNPs associated with age-specific changes of body mass index. The fGWAS model, equipped with Bayesian group lassso, will provide a useful tool for genetic and developmental analysis of complex traits or diseases.Entities:
Keywords: Bayesian approach; GWAS; Group variable selection; Longitudinal data
Year: 2015 PMID: 26478762 PMCID: PMC4605444 DOI: 10.1214/15-AOAS808
Source DB: PubMed Journal: Ann Appl Stat ISSN: 1932-6157 Impact factor: 2.083