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This repository has been archived by the owner on Apr 12, 2023. It is now read-only.
As I mentioned today, it would be good in anticipation of the paper to create a query endpoint for phenotype coverage assessment equivalent to what we did for LaySlim v GC.
As I mentioned today, it would be good in anticipation of the paper to create a query endpoint for phenotype coverage assessment equivalent to what we did for LaySlim v GC.
cc: @krageth, @kshefchek
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