Hi MIRA users, I recently tested out MIRA with error corrected PacBio reads (via PacBioToCA). After error correction our coverage was significantly lower (2.7 according to MIRA; we had a high rate of read loss through the PacBioToCA pipeline), but we ended up with a smaller number of contigs than our Illumina-only de Bruijn graph assembly and a total number of bases very close to our past assembly. While initially happy with these results, we noticed that our read mapping rate of Illumina reads to PacBio MIRA contigs (via bowtie2 with --very-sensitive option) was remarkably lower (~48%) compared to our Illumina reads mapped to Illumina-only contigs mapping rate (~97%). When we map our Illumina reads to our error corrected PacBio reads, we see a much higher mapping rate (around 84%), indicating that error correction isn't adversely affecting the process. I've looked and all contigs have reads mapping to them with decent coverage, so it's not a subset of contigs with zero alignments causing the low mapping rate. Our expected genome size is about 70Mb. Does anyone have any insight into why our mapping rate is so low? thanks, Vince -- Vince Buffalo Statistical Programmer Bioinformatics Core UC Davis Genome Center University of California, Davis "There's real poetry in the real world. Science is the poetry of reality." -Richard Dawkins