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Discussion continued in #219. |
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Discussion continued in #219. |
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I'm putting this as an "idea" here.
A common request is adding support for the current human genome release GRCh38/hg38 to VarFish. By design, VarFish is able to store variant sets from "arbitrary" genomes, it would even be able to store mouse data -- in principle. However, this underlies the following constraints.
While certainly feasible this requires a commitment of resources that the VarFish team in Berlin currently do not have. This is on our list and so far we've always postponed it until gnomAD and gnomAD SV are available for GRCh38.
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