Hello, I have two transcriptomes assemblys, one sequenced with Illumina and the other with 454. I assembled separated with Trinity. The transcriptomes are from the differents cultivars of Eragrostis curvula. I perform a blast 454vsIllumina and aligned only 4000 transcripts (-query "454" 96364 transcripts -db: "Illumina" 265309 transcripts, changing the db and query the result is similar). I expected a higher value of alignments, because even though they are differents cultivars the mayority of the transcript may be similar. Now i´am running a blast of both assembles against uniprot and i`ll compare them. I don´t know if this differences is due a low coverage of 454 reads or is possible that the expression is so different. Someone performed a similar analysis?