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 er
rors. The new Haseman-Elston (NHE) method is a least-squares-based VC metho
d for mapping of QTL in sib pairs (Elston et al.). Using simulation, we inv
estigate the robustness of the NHE to marked nonnormality, by means of the
same distributions and worst-case conditions identified by Allison et al. f
or the ML approach (i.e., 100 pairs; high residual sibling correlation). Re
sults showed that, when marked nonnormality is present, the NHE can be used
without severe type I error-rate inflation, even at very small alpha level
s.