Journal
GENETIC EPIDEMIOLOGY
Volume 29, Issue 1, Pages 12-22Publisher
WILEY
DOI: 10.1002/gepi.20075
Keywords
linkage analysis; association analysis; quantitative trait locus; iterative generalized least squares
Funding
- NCRR NIH HHS [RR03655] Funding Source: Medline
- NIDDK NIH HHS [DK57292] Funding Source: Medline
- NIGMS NIH HHS [GM28356] Funding Source: Medline
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The Haseman-Elston (HE) (Haseman and Elston [1972] Behav Genet 2:3-19) method is widely used in genetic linkage studies for quantitative traits. We propose a new version of the HE regression model, a two-level HE regression model (tHE) in which the variance-covariance structure of family data is modeled under the framework of multiple-level regression. An iterative generalized least squares (IGLS) algorithm is adopted to handle the varying variance-covariance structures across families in a simple fashion. In this way, the tHE can compete favorably with any current version of HE in that it can naturally make use of all the trait information available in any general pedigree, Simultaneously incorporate individual-level and pedigree-level covariates, marker genotypes for linkage (i.e., the number of allele shared identically by descent [IBD]), and marker alleles for association. Under the assumption of normality, the method is asymptotically equivalent to the usual variance component model for detecting linkage. For the situation where the asumption of normality is critical, a robust globally consistent estimator of the quantitative trait locus (QTL) variance is available. Complex genetic mechanisms, including gene-gene interaction, gene-environmental interaction, and imprinting, can be directly modeled in this version of HE regression. (c) 2005 Wiley-Liss, Inc.
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