I got a bacteria genome which sequencing by 454 technique and Illumina technique separately.
After run 454 reads by using MIRA and BAMBUS, I extract the longest scaffold and treat it as a backbone. I hope that I able to polish this longest scaffold by using Illumina reads to get better assembly result.
I just confusing how to use MIRA to polish my longest scaffold and get better assembly result.
Thanks again for everybody.
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