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Wiley InterScience

Biometrics

Biometrics

Volume 63 Issue 4, Pages 1079 - 1088

Published Online: 1 May 2007

©2009 International Biometric Society



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Semiparametric Regression of Multidimensional Genetic Pathway Data: Least-Squares Kernel Machines and Linear Mixed Models
Dawei Liu 1,*,Xihong Lin 2,**; and Debashis Ghosh 3,***
  1 Center for Statistical Sciences, Brown University, Providence, Rhode Island 02912, U.S.A   2 Department of Biostatistics, Harvard School of Public Health, Boston, Massachusetts 02115, U.S.A   3 Department of Biostatistics, University of Michigan, Ann Arbor, Michigan 48109, U.S.A
Correspondence to   * email: daweiliu@stat.brown.edu   ** email: xlin@hsph.harvard.edu   *** email: ghoshd@umich.edu
Copyright 2007, The International Biometric Society
KEYWORDS
BLUPs • Kernel function • Model/variable selection • Nonparametric regression • Penalized likelihood • REML • Score test • Smoothing parameter • Support vector machines

ABSTRACT

Summary .   We consider a semiparametric regression model that relates a normal outcome to covariates and a genetic pathway, where the covariate effects are modeled parametrically and the pathway effect of multiple gene expressions is modeled parametrically or nonparametrically using least-squares kernel machines (LSKMs). This unified framework allows a flexible function for the joint effect of multiple genes within a pathway by specifying a kernel function and allows for the possibility that each gene expression effect might be nonlinear and the genes within the same pathway are likely to interact with each other in a complicated way. This semiparametric model also makes it possible to test for the overall genetic pathway effect. We show that the LSKM semiparametric regression can be formulated using a linear mixed model. Estimation and inference hence can proceed within the linear mixed model framework using standard mixed model software. Both the regression coefficients of the covariate effects and the LSKM estimator of the genetic pathway effect can be obtained using the best linear unbiased predictor in the corresponding linear mixed model formulation. The smoothing parameter and the kernel parameter can be estimated as variance components using restricted maximum likelihood. A score test is developed to test for the genetic pathway effect. Model/variable selection within the LSKM framework is discussed. The methods are illustrated using a prostate cancer data set and evaluated using simulations.


Received September 2005. Revised November 2006. Accepted January 2007.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1541-0420.2007.00799.x About DOI

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