We constructed a bacterial artificial chromosome (BAC)-based physical map o
f chromosomes 2 and 3 of Drosophila melanogaster, which constitute 81% of t
he genome. Sequence tagged site (STS) content, restriction fingerprinting,
and polytene chromosome in situ hybridization approaches were integrated to
produce a map spanning the euchromatin. Three of five remaining gaps are i
n repeat-rich regions near the centromeres. A tiling path of clones spannin
g this map and STS maps of chromosomes X and 4 was sequenced to low coverag
e; the maps and tiling path sequence were used to support and verify the wh
ole-genome sequence assembly, and tiling path BACs were used as templates i
n sequence finishing.