a project of vibrio complete genome sequencing, next generation 454 and solexa got the genome draft.
super-integron in many vibrios, such as, vibrio cholera . super-integron, about 100 kb, within much short repeats (120 bp) . PCR to close gap, there is no PCR amplification product
how should i do now? any suggestion?
thank you
super-integron in many vibrios, such as, vibrio cholera . super-integron, about 100 kb, within much short repeats (120 bp) . PCR to close gap, there is no PCR amplification product
how should i do now? any suggestion?
thank you