We model functions that use genetic information as input and trait informat
ion as output to understand genetic linkage in complex diseases. Using simu
lated data from GAW11, we have applied categorical classification methods a
nd neural network analysis. We use sharing at selected markers as input, an
d the classification of the sib pair (for example, affected-affected or aff
ected-unaffected) as output. In addition, our methods include environmental
risk factors as predictors of phenotype. Categorical and neural network me
thods each led to results consistent with findings from other methods such
as the logistic regression method of Rice et al. [this issue]. Post-analysi
s comparison with the GAW11 answers showed that these methods are capable o
f detecting correct signals in a single replicate. One advantage of our met
hods is that they allow analysis of the entire genome at once, so that inte
ractions among multiple trait-influencing loci may be detected. Furthermore
, these methods can use a variety of sib pairs rather than affected pairs o
nly. (C) 1999 Wiley-Liss, Inc.