Abstract
Abstract
The purpose of these analyses was to determine if incorporating or adjusting for covariates in genetic analyses helped or hindered in genetic analyses, specifically heritability and linkage analyses. To study this question, two types of covariate models were used in the simulated Genetic Analysis Workshop 14 dataset in which the true gene locations are known. All four populations of one replicate were combined for the analyses. The first model included typical covariates of sex and cohort (population) and the second included the typical covariates and also those related endophenotypes that are thought to be associated with the trait (phenotypes A, B, C, D, E, F, G, H, I, J, K, and L). A final best fit model produced in the heritability analyses was used for linkage. Linkage for disease genes D1, D3, and D4 were localized using models with and without the covariates. The use of inclusion of covariates did not appear to have any consistent advantage or disadvantage for the different phenotypes in regards to gene localization or false positive rate.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference6 articles.
1. Lange K, Westlake J, Spence MA: Extensions to pedigree analysis. III. Variance components by the scoring method. Am J Hum Genet. 1976, 39: 485-491.
2. Amos CI: Robust variance-components approach for assessing genetic linkage in pedigrees. Am J Hum Genet. 1994, 54: 535-543.
3. Goldgar DE, Oniki RS: Comparison of a multipoint identity-by-descent method with parametric multipoint linkage analysis for mapping quantitative traits. Am J Hum Genet. 1992, 50: 598-606.
4. Almasy L, Williams J, Dyer T, Blangero J: Quantitative trait locus detection using combined linkage/disequilibrium analysis. Genet Epidemiol. 1999, 17 (Suppl 1): S31-S36.
5. Duggirala R, Williams JT, Williams-Blangero S, Blangero J: A variance component approach to dichotomous trait linkage analysis using a threshold model. Genet Epidemiol. 1997, 14: 987-992. 10.1002/(SICI)1098-2272(1997)14:6<987::AID-GEPI71>3.0.CO;2-G.
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