Hi all,
I understand that with Pacbio error rate (~15%), it is not really suitable for SNP calling.
This is maybe a naive question, but I was wondering if we have, for example, a really high coverage sequencing of a bacteria (>200X), wouldn't it make it possible to call SNP anyway?
If so, what would be the most cleaver way to do that? Try to do the "classic" way, align to a reference genome and detect variants (is there any tool doing that?). Or maybe perform a genome assembly, and then align the assembly to the reference ?
Has anyone tried that already?
Thanks in advance for your inputs
When you have 200x coverage, it might be easiest to simply generate consensus sequence (reads of insert) and then call variants from those. That way you avoid the problems of high error rates.
Ok that was what I thought, thanks for your help.