Summary We propose in this article a powerful testing procedure for detecting a gene effect on a continuous outcome in the presence of possible gene–gene interactions (epistasis) in a gene set, e.g., a genetic pathway or network. Traditional tests for
this purpose require a large number of degrees of freedom by testing the main effect and all the corresponding interactions under a parametric assumption, and hence suffer from low power. In this article, we propose a powerful kernel machine based test. Specifically, our test is based on a
garrote kernel method and is constructed as a score test. Here, the term garrote refers to an extra nonnegative parameter that is multiplied to the covariate of interest so that our score test can be formulated in terms of this nonnegative parameter. A key feature of the proposed test is that
it is flexible and developed for both parametric and nonparametric models within a unified framework, and is more powerful than the standard test by accounting for the correlation among genes and hence often uses a much smaller degrees of freedom. We investigate the theoretical properties
of the proposed test. We evaluate its finite sample performance using simulation studies, and apply the method to the Michigan prostate cancer gene expression data.
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Document Type: Research Article
Department of Statistics, North Carolina State University, Raleigh, North Carolina 27695, U.S.A.
Department of Biostatistics, Harvard School of Public Health, Boston, Massachusetts 02115, U.S.A.
Publication date: 2011-12-01