Extending the method for linkage analysis [Zhao et al., 1998a: Am. J. Med. Genet. 77:366-383; 1998b: Am. J. Med. Genet. 79:49-61], this article describes a method for the linkage-disequilibrium analysis, and for combining linkage and linkage-disequilibrium analyses. As highly dense markers are incre
Statistical multilocus methods for disequilibrium analysis in complex traits
โ Scribed by Jurg Ott; Josephine Hoh
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 134 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1059-7794
- DOI
- 10.1002/humu.25
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โฆ Synopsis
Hundreds of thousands of SNP markers are being generated with the purpose of carrying out casecontrol association studies for complex traits, which are thought to be due to multiple underlying susceptibility genes. The number of markers is typically much larger than the number of observations so that joint analysis of marker genotypes and their interactions is not feasible. We discuss a two-stage approach to first select a small subset of markers and then model the effects of the selected markers on disease. Examples of two procedures for marker selection are given with subsequent modeling of main and interaction effects. The approaches are applied to a data set with 89 SNPs in lieu of a genome screen with many more markers. Hum Mutat 17:285-288, 2001.
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