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Clinical-Genomics / scout

VCF visualization interface
https://clinical-genomics.github.io/scout
BSD 3-Clause "New" or "Revised" License
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Store pathogenic variants in own collection #167

Closed moonso closed 7 years ago

moonso commented 8 years ago

Pathogenic variants should be added when case is solved and closed

robinandeer commented 8 years ago

Tell me if we should show this somehow, or is this only for internal purposes?

moonso commented 8 years ago

I'm not completely sure if we will store them in their own collection but they will be accessible. Is there anything more we want to do with them except exporting?

henrikstranneheim commented 8 years ago

They should be accessible for the aggregate data layer and as you said exportable for downstream analysis.

moonso commented 7 years ago

I consider this covered in #320 so closing