We compared the statistical performance of sibpair-based and variance components approaches to multipoint linkage analysis of a quantitative trait in unselected samples. As a benchmark dataset, we used the simulated family data from Genetic Analysis Workshop 10 [Goldin et al., 1997], and each method
A variance component approach to dichotomous trait linkage analysis using a threshold model
β Scribed by Ravindranath Duggirala; Jeff T. Williams; Sarah Williams-Blangero; John Blangero
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 65 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
β¦ Synopsis
We developed and utilized a multipoint variance components method to test for linkage between a disease trait and markers on chromosome 5 in the simulated data provided in GAW10 Problem 2. We demonstrated that the discrete trait variance components method recovers unbiased estimates of quantitative trait locus (QTL) location and reasonable estimates of effect size. We also showed that dichotomization of (a continuous trait such as) Q1 diminished the power to detect linkage compared to direct analysis of Q1, and that extended pedigree analyses provided superior power to detect linkage compared to those in nuclear families.
π SIMILAR VOLUMES
We investigated the statistical properties of a variance components method for quantitative trait linkage analysis using nuclear families and extended pedigrees.
## Abstract We report further evidence for our previous suggestion [Garner et al., 2001: Am J Hum Genet 68:1061β1064] of a locus on 5q predisposing to bipolar I disorder (BPβI) in an extended Costa Rican pedigree. We genotyped additional microsatellite markers in this region and applied a multiβpoi