Fluoresence in situ hybridization (FISH) was used to localize cosmids
to regions of human chromosome 10. A total of 301 cosmids were selecte
d randomly from a flow-sorted human chromosome 10 cosmid library const
ructed from human x hamster cell line 762-8A and arrayed in microtiter
storage dishes. Over 70% (211/301) of the cosmids mapped to unique re
gions of chromosome 10. About 7% (22/301) produced multiple hybridizat
ion signals indicative of chimeric clones or sequences repeated at low
copy number. Three cosmids (3/301, or 1%) hybridized to the centromer
ic regions of chromosome 10 and one or more other human chromosomes. A
bout 19% (59/301) consisted mostly or- entirely of hamster DNA inserts
, and about 2% (6/301) appeared to be nonrecombinants.