Closed fangbohao closed 2 days ago
Hi @fangbohao, you can skip the partitioning, it is not a mandatory step. We recommend creating subsets of contigs, when possible and if it makes sense for the specific analysis, to reduce the computational work for PGGB.
Thanks for your comments, Andrea!
Hi, I was wondering if I could just skip the sequence partitioning because there is a chromosome-level genome provided by the VGP project. Could I just subset chromosomes based on the VGP reference genome for my HiFi haplotype contigs? Is there any hidden issue if I skip this step?
Thanks! Bohao