Literature DB >> 27488097

Prioritizing individual genetic variants after kernel machine testing using variable selection.

Qianchuan He1, Tianxi Cai2, Yang Liu1, Ni Zhao1, Quaker E Harmon3, Lynn M Almli4, Elisabeth B Binder5, Stephanie M Engel6, Kerry J Ressler7, Karen N Conneely8, Xihong Lin2, Michael C Wu1.   

Abstract

Kernel machine learning methods, such as the SNP-set kernel association test (SKAT), have been widely used to test associations between traits and genetic polymorphisms. In contrast to traditional single-SNP analysis methods, these methods are designed to examine the joint effect of a set of related SNPs (such as a group of SNPs within a gene or a pathway) and are able to identify sets of SNPs that are associated with the trait of interest. However, as with many multi-SNP testing approaches, kernel machine testing can draw conclusion only at the SNP-set level, and does not directly inform on which one(s) of the identified SNP set is actually driving the associations. A recently proposed procedure, KerNel Iterative Feature Extraction (KNIFE), provides a general framework for incorporating variable selection into kernel machine methods. In this article, we focus on quantitative traits and relatively common SNPs, and adapt the KNIFE procedure to genetic association studies and propose an approach to identify driver SNPs after the application of SKAT to gene set analysis. Our approach accommodates several kernels that are widely used in SNP analysis, such as the linear kernel and the Identity by State (IBS) kernel. The proposed approach provides practically useful utilities to prioritize SNPs, and fills the gap between SNP set analysis and biological functional studies. Both simulation studies and real data application are used to demonstrate the proposed approach.
© 2016 WILEY PERIODICALS, INC.

Entities:  

Keywords:  KNIFE; genetic association studies; kernel machine methods; set-based; variable selection

Mesh:

Substances:

Year:  2016        PMID: 27488097      PMCID: PMC5118060          DOI: 10.1002/gepi.21993

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


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