Amplification of known putative genes using BAC clone samples. F, M and R probes were designed at the 5'-end, middle and 3'-end portion of the Mj024A04-sequence as described in the result. The putative genes (indicated in left column) were detected with BAC clones that showed different hybridization patterns with F, M and R probes (indicated in top line). Three BAC clones for each hybridization group were tested. Reactions with three BAC clones that showed no signal (negative control: neg), Mj024A04 (positive control: pos) and without templates (-) are also included.
Koyama et al. BMC Genomics 2010 11:141 doi:10.1186/1471-2164-11-141