Entering edit mode
6.3 years ago
nancy
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90
To what extent does a de novo genome need to be assembled for it to be used as a reference? If I have a de novo assembly for a large mammalian genome comprising of a under 1M contigs (Illumina + PacBio), and I want to call SNPs against this reference from samples that have been sequenced (shallow 5x-10x Illumina short read data), will it work well?
What would be the parameters to tweak for alignment, variant calling, and what would be the warning signs to look out for? Thank you
1,000,000 (one million) contigs? Or 1,000 (one thousand) contigs?