| Literature DB >> 30247537 |
Bo Chen1, Radu V Craiu1, Lei Sun1.
Abstract
X-chromosome is often excluded from the so called "whole-genome" association studies due to the differences it exhibits between males and females. One particular analytical challenge is the unknown status of X-inactivation, where one of the two X-chromosome variants in females may be randomly selected to be silenced. In the absence of biological evidence in favor of one specific model, we consider a Bayesian model averaging framework that offers a principled way to account for the inherent model uncertainty, providing model averaging-based posterior density intervals and Bayes factors. We examine the inferential properties of the proposed methods via extensive simulation studies, and we apply the methods to a genetic association study of an intestinal disease occurring in about 20% of cystic fibrosis patients. Compared with the results previously reported assuming the presence of inactivation, we show that the proposed Bayesian methods provide more feature-rich quantities that are useful in practice.Entities:
Keywords: Bayes factors; Bayesian methods; Bayesian model averaging; Genome-wide association studies; Markov chain Monte Carlo; Model uncertainty; Ranking; X-chromosome
Mesh:
Year: 2020 PMID: 30247537 DOI: 10.1093/biostatistics/kxy049
Source DB: PubMed Journal: Biostatistics ISSN: 1465-4644 Impact factor: 5.899