Testing for linkage under robust genetic models

R. Guerra, Y. Wan, A. Jia, C. I. Amos, J. C. Cohen

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

Robust genetic models are used to assess linkage between a quantitative trait and genetic variation at a specific locus using allele-sharing data. Little is known about the relative performance of different possible significance tests under these models. Under the robust variance components model approach there are several alternatives: standard Wald and likelihood ratio tests, a quasilikelihood Wald test, and a Monte Carlo test. This paper reports on the relative performance (significance level and power) of the robust sibling pair test and the different alternatives under the robust variance components model. Simulations show that (1) for a fixed sample size of nuclear families, the variance components model approach is more powerful than the robust sibling pair approach; (2) when the number of nuclear families is at least ~ 100 and heritability at the trait locus is moderate to high (> 0.20) all tests based on the variance components model are equally effective; (3) when the number of nuclear families is less than ~ 100 or heritability at the trait locus is low (< 0.20), on balance, the Monte Carlo test provides the best power and is the most valid. The different testing procedures are applied to determine which are able to detect the known association between low density lipoprotein cholesterol and the common genotypes at the locus encoding apolipoprotein E. Results from this application show that the robust sibling pair method may be more effective in practice than that indicated by simulations.

Original languageEnglish (US)
Pages (from-to)146-153
Number of pages8
JournalHuman Heredity
Volume49
Issue number3
DOIs
StatePublished - Jun 1 1999

Keywords

  • Linkage
  • Monte Carlo
  • Significance test
  • Variance components

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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