Informative Bayesian Model Selection: a method for identifying interactions in genome-wide data

被引:1
|
作者
Aflakparast, Mehran [1 ,2 ]
Masoudi-Nejad, Ali [1 ]
Bozorgmehr, Joseph H. [1 ]
Visweswaran, Shyam [3 ]
机构
[1] Univ Tehran, Inst Biochem & Biophys, Lab Syst Biol & Bioinformat LBB, Tehran 14174, Iran
[2] Vrije Univ Amsterdam, Fac Sci, Dept Math, Amsterdam, Netherlands
[3] Univ Pittsburgh, Dept Biomed Informat, Pittsburgh, PA 15260 USA
关键词
DETECTING GENE-GENE; EPISTASIS; ASSOCIATION; CHALLENGES; REVEALS; APOE;
D O I
10.1039/c4mb00123k
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In high-dimensional genome-wide (GWA) data, a key challenge is to detect genomic variants that interact in a nonlinear fashion in their association with disease. Identifying such genomic interactions is important for elucidating the inheritance of complex phenotypes and diseases. In this paper, we introduce a new computational method called Informative Bayesian Model Selection (IBMS) that leverages correlation among variants in GWA data due to the linkage disequilibrium to identify interactions accurately in a computationally efficient manner. IBMS combines several statistical methods including canonical correlation analysis, logistic regression analysis, and a Bayesians statistical measure of evaluating interactions. Compared to BOOST and BEAM that are two widely used methods for detecting genomic interactions, IBMS had significantly higher power when evaluated on synthetic data. Furthermore, when applied to Alzheimer's disease GWA data, IBMS identified previously reported interactions. IBMS is a useful method for identifying variants in GWA data, and software that implements IBMS is freely available online from http://lbb.ut.ac.ir/Download/LBBsoft/IBMS.
引用
收藏
页码:2654 / 2662
页数:9
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