We develop a mixed-model approach for QTL analysis in crosses between outbr
ed lines that allows for QTL segregation within lines as well as for differ
ences in mean QTL effects between lines. We also propose a method called "s
egment mapping" that is based in partitioning the genome in a series of seg
ments. The expected change in mean according to percentage of breed origin,
together with the genetic variance associated with each segment, is estima
ted using maximum likelihood. The method also allows the estimation of diff
erences in additive variances between the parental lines. Completely fixed
random and mixed models together with segment mapping are compared via simu
lation. The segment mapping and mixed-model behaviors are similar to those
of classical methods, either the fixed or random models, under simple genet
ic models (a single QTL with alternative alleles fixed in each line), where
as they provide less biased estimates and have higher power than fixed or r
andom models in more complex situations, i.e., when the QTL are segregating
within the parental lines. The segment mapping approach is particularly us
eful to determining which chromosome regions are likely to contain QTL when
these are linked.