Closed zhoudreames closed 2 years ago
Sorry, I only noticed this issue now while doing something else. This is a good question, and you're probably best looking at the paper https://www.biorxiv.org/content/10.1101/2022.07.09.499321v1.abstract for a discussion on it.
with vg construct
graphs are created from
reads -> map-against-reference -> variant calls -> VCF -> graph
whereas the graphs presented here are created from
reads->assembled genome-> multiple genome alignment -> graph
by using the multiple alignment, we hope to have better representation of complex variation, particularly in regions that are not easily represented along the reference.
thanks~
I'm very curious about why I can't adapt to vg to construct pangenome Is there any limitation in vg method? we used hifi data to obtain multiple haplotype-revolved assemblies,but I don't know how to choose which method to construct the pangenome? Is there any recommendation ? thanks~