Hi, I wonder if someone can offer some insight. I have performed an accurate de novo assembly with poly-a/t trimming. I get all reads assembled, and no singlets, into around 66k contigs. Around 27k of these are large contigs, with the largest being ~25k bases long. This does not make much sense to me as I constructed a 3' target cDNA library (454 FLX). I can envisage multiple open reading frames may create longer transcripts but 25k seems dodgy to me. Any thoughts? Best, Jack