The human X chromosome is associated with a large number of disease ph
enotypes, principally because of its unique mode of inheritance that t
ends to reveal all recessive disorders in males. With the longer term
goal of identifying and characterizing most of these genes, we have ad
opted a chromosome-wide strategy to establish a YAC contig map. We hav
e performed >3250 inter Alu-PCR product hybridizations to identify ove
rlaps between YAC clones. Positional information associated with many
of these YAC clones has been derived from our Reference Library Databa
se and a variety of other public sources. We have constructed a YAC co
ntig map of the X chromosome covering 125 Mb of DNA in 25 contigs and
containing 906 YAC clones. These contigs have been verified extensivel
y by FISH and by gel and hybridization fingerprinting techniques. This
independently derived map exceeds the coverage of recently reported X
chromosome maps built as part of whole-genome YAC maps.