Using graph theory, we present a theoretical basis for mapping oligogenes in the joint presence of multiple phenotypic measurements of both quantitative and qualitative types. Various statistical models proposed earlier for several traits of solely single type are special cases of the unified approa
Mapping multiple genes for quantitative or complex traits
โ Scribed by Hsiu-Khuern Tang; David Siegmund
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 95 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0741-0395
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โฆ Synopsis
Abstract
Models for complex and quantitative traits that involve multiple, possibly interacting, genes are described. Methods of linkage analysis are developed that utilize special features of these models, and their power is compared with that of simple genome scans that ignore these special features. Our calculations show that for familyโbased nonparametric linkage analysis in human genetics, in contrast to experimental genetics, there are limits to the increase in power that can be achieved by correctly modeling geneโgene interactions. In particular, the noncentrality parameter of likelihoodโbased statistics to detect single gene effects involves both single gene and interaction components of variance, so even when the interaction components of variance are relatively large, the incremental power from a statistic designed to detect both single gene and interaction effects is often quite modest. We carry out our analysis with the assistance of a parameterization that allows us to compute score statistics, noncentrality parameters, and Fisher information matrices reasonably explicitly. Genet. Epidemiol. 22:313โ327, 2002. ยฉ 2002 WileyโLiss, Inc.
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