Linkage strategies for genetically complex traits. I. Multilocus models
- PMID: 2301392
- PMCID: PMC1684987
Linkage strategies for genetically complex traits. I. Multilocus models
Abstract
In order to investigate linkage detection strategies for genetically complex traits, multilocus models of inheritance need to be specified. Here, two types of multilocus model are described: (1) a multiplicative model, representing epistasis (interaction) among loci, and (2) an additive model, which is shown to closely approximate genetic heterogeneity, which is characterized by no interlocus interaction. A ratio lambda R of risk for type R relatives that is compared with population prevalence is defined. For a single-locus model, lambda R - 1 decreases by a factor of two with each degree of relationship. The same holds true for an additive multilocus model. For a multiplicative (epistasis) model, lambda R - 1 decreases more rapidly than by a factor of two with degree of relationship. Examination of lambda R values for various classes of relatives can potentially suggest the presence of multiple loci and epistasis. For example, data for schizophrenia suggest multiple loci in interaction. It is shown in the second paper of this series that lambda R is the critical parameter in determining power to detect linkage by using affected relative pairs.
Comment in
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Cutting a Gordian knot in the linkage analysis of complex human traits.Am J Hum Genet. 1990 Feb;46(2):219-21. Am J Hum Genet. 1990. PMID: 2405655 Free PMC article. Review. No abstract available.
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Inflated false-positive rates in Hardy-Weinberg and linkage-equilibrium tests are due to sampling on the basis of rare familial phenotypes in finite populations.Am J Hum Genet. 2000 Jul;67(1):258-9. doi: 10.1086/302964. Am J Hum Genet. 2000. PMID: 10848498 Free PMC article. No abstract available.
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