Back to Search
Start Over
An Extension of the Regression of Offspring on Mid-Parent to Test for Association and Estimate Locus-Specific Heritability: The Revised ROMP Method
- Source :
- Annals of Human Genetics. :071203214149001
- Publication Year :
- 2007
- Publisher :
- Wiley, 2007.
-
Abstract
- Summary 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.
- Subjects :
- Parents
Genetics
Candidate gene
Korea
Polymorphism, Genetic
Quantitative Trait Loci
Fibrinogen
Locus (genetics)
Heritability
Quantitative trait locus
Biology
Confidence interval
Regression
Nuclear Family
Standard error
Cardiovascular Diseases
Research Design
Multigene Family
Statistics
Humans
Regression Analysis
Computer Simulation
Genetics (clinical)
Type I and type II errors
Subjects
Details
- ISSN :
- 14691809 and 00034800
- Database :
- OpenAIRE
- Journal :
- Annals of Human Genetics
- Accession number :
- edsair.doi.dedup.....bc90509538624044aecddd90aa080e4a
- Full Text :
- https://doi.org/10.1111/j.1469-1809.2007.00401.x