We have previously demonstrated the capability of the Fosmid vector ba
sed on Escherichia coli F-Factor replicon to stably propagate cosmid-s
ized human genomic DNA fragments. Using the Fosmid vector, we have con
structed and arrayed a 10x human chromosome 22-specific library, partl
y by picking human positive clones from a total Fosmid library constru
cted using DNA from human-hamster hybrid cell line containing human ch
romosome 22, and partly by using flow-sorted chromosomal DNA. The clon
es and physical contig maps of the clones in the library will serve as
a valuable resource for detailed analysis of the chromosome by somal
regions of interest spanning several hundred kilobases to a megabase,
it is necessary to rapidly identify subsets of the Fosmid clones from
the library that cover such regions. In this report, we describe a met
hod of using random amplification products derived from YAC clones to
rapidly identify a subset of Fosmid clones that cover a specific genom
ic subregion.