Testing the robustness of the new Haseman-Elston quantitative-trait loci-mapping procedure
- PMID: 10820126
- PMCID: PMC1287085
- DOI: 10.1086/302966
Testing the robustness of the new Haseman-Elston quantitative-trait loci-mapping procedure
Abstract
Variance components (VC) techniques have emerged as among the more powerful methods for detection of quantitative-trait loci (QTL) in linkage analysis. Allison et al. found that, with particularly marked leptokurtosis in the phenotypic distribution and moderate-to-high residual sibling correlation, maximum likelihood (ML) VC methods may produce a severe excess of type I errors. The new Haseman-Elston (NHE) method is a least-squares-based VC method for mapping of QTL in sib pairs (Elston et al.). Using simulation, we investigate the robustness of the NHE to marked nonnormality, by means of the same distributions and worst-case conditions identified by Allison et al. for the ML approach (i.e., 100 pairs; high residual sibling correlation). Results showed that, when marked nonnormality is present, the NHE can be used without severe type I error-rate inflation, even at very small alpha levels.
References
-
- Allison DB, Schork NJ (1997) Selected methodological issues in meiotic mapping of obesity genes in humans: issues of power and efficiency. Behav Genet 27:401–421 - PubMed
-
- Amos CI, Laing AE (1993) A comparison of univariate and multivariate tests for genetic linkage. Genet Epidemiol 10:671–676 - PubMed
-
- Dolan CV, Boomsma DI (1998) Optimal selection of sib pairs from random samples for linkage analysis of a QTL using the EDAC Test. Behav Genet 28:197–206 - PubMed
-
- Elston RC, Buxbaum S, Jacobs KB, Olson JM. Haseman and Elston revisited. Genet Epidemiol (in press) - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources