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ClinGen / gene-and-variant-curation-tools

ClinGen's gene and variant curation interfaces (GCI & VCI). Developed by Stanford ClinGen team.
https://curation.clinicalgenome.org/
MIT License
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Display warning when user is viewing duplicated PMIDs in the case/seg table #125

Closed cgpreston closed 1 year ago

cgpreston commented 2 years ago

To enable curators to identify and eliminate double counting in the case/seg tab:

  1. Provide a visual cue the length of the column for PMIDs that are duplicated
  2. Display warning symbols and hover-over language when duplicate PMIDs are displayed in the Case/Seg tab 
  3. The mockup slides are here, with the relevant slides being "feature 1" (slides 7-11) https://docs.google.com/presentation/d/1Y4oi4lP-72xrDK1AzlAxTWwVlV2XKRPzBrl9rToc7lg/edit#slide=id.g1104afc3cf9_0_86

SP ticket: https://broadinstitute.atlassian.net/browse/CGSP-617

liammulh commented 1 year ago

I think as of https://github.com/ClinGen/gci-vci-aws/commit/7871db11673e53faa3936157fb0ffe8d6fdf38e2, feature 1 has been implemented.

liammulh commented 1 year ago

This is now in prod, closing.