PacBio self-error correction (PBcR) is possible at such high coverages. Then you can use Falcon assembler or CANU.
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Hi, everyone. I have a project about 50M fungi diploid denovo assembly. I had assembly 37M fungi haploid with pacbio reads and illuminate and Miseq reads. For haploid genome, I used Ectool and HGAP3. But for diploid genome, I have doubt about how to correct subreads, and which assembler to use.
And I have about 50x subreads.
Thanks!
My firt thought is use SOAP2 to get diploid contigs,then use these contigs and PE reads to correct subreads ,inally use FALCON.
PacBio self-error correction (PBcR) is possible at such high coverages. Then you can use Falcon assembler or CANU.
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