Power of multipoint identity‐by‐descent methods to detect linkage using variance component models
- 6 December 2001
- journal article
- research article
- Published by Wiley in Genetic Epidemiology
- Vol. 21 (4) , 285-298
- https://doi.org/10.1002/gepi.1035
Abstract
Multipoint linkage analysis gives increased power over single‐point analysis to detect linkage for quantitative trait loci (QTL). Besides increased power, the use of multipoint methods makes it possible to estimate not only the location but also the magnitude of the QTL. Currently, two methods are commonly used for calculating multipoint identity‐by‐descent (IBD) allele‐sharing estimates for pedigrees of moderate sizes. The method of Fulker et al. is based on multiple regression of the IBD status at the observed marker loci, whereas the hidden Markov model approach of Kruglyak and Lander estimates the true inheritance distribution at each chromosomal location. Simulation studies of full sibs and nuclear pedigrees show that the two methods for estimating multipoint IBD scores may give very different estimates for a pair of relatives and that a small increase in power to detect linkage can be obtained by using the hidden Markov model compared with the regression method. Genet. Epidemiol. 21:285–298, 2001.Keywords
This publication has 8 references indexed in Scilit:
- Exact Multipoint Quantitative-Trait Linkage Analysis in Pedigrees by Variance ComponentsAmerican Journal of Human Genetics, 2000
- Multipoint Quantitative-Trait Linkage Analysis in General PedigreesAmerican Journal of Human Genetics, 1998
- Faster Multipoint Linkage Analysis Using Fourier TransformsJournal of Computational Biology, 1998
- Power of variance component linkage analysis to detect epistasisGenetic Epidemiology, 1997
- Asymptotic Properties of Maximum Likelihood Estimators and Likelihood Ratio Tests under Nonstandard ConditionsJournal of the American Statistical Association, 1987
- Construction of multilocus genetic linkage maps in humans.Proceedings of the National Academy of Sciences, 1987
- Extensions to multivariate normal models for pedigree analysisAnnals of Human Genetics, 1982
- Extensions to pedigree analysis III. Variance components by the scoring methodAnnals of Human Genetics, 1976