Improvement in localization of disease susceptibility genes by simultaneous
consideration of multiple interacting loci was assessed using the Genetic
Analysis Workshop 12 simulated data. Evidence of linkage at primary loci wa
s used to weight families for analyses at secondary loci. To identify regio
ns linked to disease susceptibility genes, parametric and allele-sharing ge
nome scans were performed in the extended pedigrees and nuclear families, r
espectively. The position of the peak allele-sharing lod was used as the es
timate of a disease gene location. In weighted analyses, the positions wher
e the greatest lod increases occurred were taken as alternative estimates o
f the gene locations. Variability of the location estimates of disease gene
s given by the unweighted and weighted analyses was compared. Similar analy
ses were carried out using true disease loci to determine weights. Weighted
analyses did not in general improve the localization of disease genes in t
his data set, even with a large sample of 1,928 nuclear families, due to th
e features of the underlying additive liability threshold model. (C) 2001 W
iley-Liss, Inc.