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An Extension of the Regression of Offspring on Mid-Parent to Test for Association and Estimate Locus-Specific Heritability: The Revised ROMP Method
Authors:M.-H. Roy-Gagnon  R. A. Mathias  M. D. Fallin  S. H. Jee  K. W. Broman   A. F. Wilson
Affiliation:Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, NIH, Baltimore, MD;Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD;Department of Epidemiology and Health Promotion, Graduate School of Public Health, Yonsei University, Seoul, Korea;Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD
Abstract:The Regression of Offspring on Mid-Parent (ROMP) method is a test of association between a quantitative trait and a candidate locus. ROMP estimates the trait heritability and the heritability attributable to a locus and requires genotyping the offspring only. In this study, the theory underlying ROMP was revised (ROMPrev) and extended. Computer simulations were used to determine the type I error and power of the test of association, and the accuracy of the locus-specific heritability estimate. The ROMPrev test had good power at the 5% significance level with properly controlled type I error. Locus-specific heritability estimates were, on average, close to simulated values. For non-zero locus-specific heritability, the proposed standard error was downwardly biased, yielding reduced coverage of 95% confidence intervals. A bootstrap approach with proper coverage is suggested as a second step for loci of interest.
ROMPrev was applied to a study of cardiovascular-related traits to illustrate its use. An association between polymorphisms within the fibrinogen gene cluster and plasma fibrinogen was detected (p < 0.005) that accounted for 29% of the estimated fibrinogen heritability. The ROMPrev method provides a computationally fast and simple way of testing for association and obtaining accurate estimates of locus-specific heritability while minimizing the genotyping required.
Keywords:association tests    quantitative trait    parent-offspring trios    candidate gene    cardiovascular disease
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