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The bcftools wrangling that was required to get the variant calls to end up in the right block groups makes me think that gen should support some of these reassigments. Contig names I can see as being out of scope, but for samples we should be able to either import a vcf into a sample regardless of the sample name in the vcf, or have an operation where a new block_group is created by taking the union of two block_groups.
This document should be expanded with more interpretation and downstream analysis of the GFA files, and use of gen branching and checkout when switching strategies from variant stacking to genome alignment.