Hi guys,

Congrats on the release. For this next one, one focus, in my opinion, should
be on analyzing variants in the context of sequencing data. This includes
infrastructure for things like calling variants (in DNA and RNA), as well as
determining their effects (e.g., coding and splicing changes). It would be
good if we could come up with a plan. If we had one, we could commit some
resources here to the problem.

Is anyone willing to help out on this? What do you guys think?

Thanks,
Michael

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