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Publication Detail

Title: Adaptive Set-Based Methods for Association Testing.

Authors: Su, Yu-Chen; Gauderman, William James; Berhane, Kiros; Lewinger, Juan Pablo

Published In Genet Epidemiol, (2016 Feb)

Abstract: With a typical sample size of a few thousand subjects, a single genome-wide association study (GWAS) using traditional one single nucleotide polymorphism (SNP)-at-a-time methods can only detect genetic variants conferring a sizable effect on disease risk. Set-based methods, which analyze sets of SNPs jointly, can detect variants with smaller effects acting within a gene, a pathway, or other biologically relevant sets. Although self-contained set-based methods (those that test sets of variants without regard to variants not in the set) are generally more powerful than competitive set-based approaches (those that rely on comparison of variants in the set of interest with variants not in the set), there is no consensus as to which self-contained methods are best. In particular, several self-contained set tests have been proposed to directly or indirectly "adapt" to the a priori unknown proportion and distribution of effects of the truly associated SNPs in the set, which is a major determinant of their power. A popular adaptive set-based test is the adaptive rank truncated product (ARTP), which seeks the set of SNPs that yields the best-combined evidence of association. We compared the standard ARTP, several ARTP variations we introduced, and other adaptive methods in a comprehensive simulation study to evaluate their performance. We used permutations to assess significance for all the methods and thus provide a level playing field for comparison. We found the standard ARTP test to have the highest power across our simulations followed closely by the global model of random effects (GMRE) and a least absolute shrinkage and selection operator (LASSO)-based test.

PubMed ID: 26707371 Exiting the NIEHS site

MeSH Terms: Computer Simulation; Genetic Predisposition to Disease; Genome-Wide Association Study/methods*; Humans; Models, Genetic*; Polymorphism, Single Nucleotide/genetics*; Regression Analysis; Risk; Sample Size

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