| Literature DB >> 27027515 |
Olga A Vsevolozhskaya1, Dmitri V Zaykin2, David A Barondess3, Xiaoren Tong3, Sneha Jadhav4, Qing Lu3.
Abstract
Recent technological advances equipped researchers with capabilities that go beyond traditional genotyping of loci known to be polymorphic in a general population. Genetic sequences of study participants can now be assessed directly. This capability removed technology-driven bias toward scoring predominantly common polymorphisms and let researchers reveal a wealth of rare and sample-specific variants. Although the relative contributions of rare and common polymorphisms to trait variation are being debated, researchers are faced with the need for new statistical tools for simultaneous evaluation of all variants within a region. Several research groups demonstrated flexibility and good statistical power of the functional linear model approach. In this work we extend previous developments to allow inclusion of multiple traits and adjustment for additional covariates. Our functional approach is unique in that it provides a nuanced depiction of effects and interactions for the variables in the model by representing them as curves varying over a genetic region. We demonstrate flexibility and competitive power of our approach by contrasting its performance with commonly used statistical tools and illustrate its potential for discovery and characterization of genetic architecture of complex traits using sequencing data from the Dallas Heart Study. Published 2016. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Keywords: functional analysis; genome-wide association studies; multivariate analysis; pleiotropy; qualitative traits; quantitative traits; sequencing studies
Mesh:
Substances:
Year: 2016 PMID: 27027515 PMCID: PMC4817279 DOI: 10.1002/gepi.21955
Source DB: PubMed Journal: Genet Epidemiol ISSN: 0741-0395 Impact factor: 2.135