Change log workbench 30

Features:

  • Feature | ACMG SNV | Add note

  • Feature | Add report service activity in dashboard

  • Feature | Add template name change activity in dashboard

  • Feature | Add template upload activity in dashboard

  • Feature | Import Gene Interpretation from Curate

  • Feature | Enable kit management in organization settings

  • Feature | New Phenomeld filter added

  • Feature | Presets | Gene list | Search for gene list name

  • Feature | Var page | Add Genomenon linkout to clinical significance

  • Feature | Display varcaller in varpage

  • Feature | Varpage | Enrich related cases

  • Feature | Gene list | add NCBI ID to genes in gene list in database

  • Feature | Validation of variant retrieval. When system is degraded this will alert users not to work on cases with incomplete variant data.

Enhancement:

  • Enhancement | Visualization - add tracks order

  • Enhancement | Visualization | Change default locus zoom for BigWig

  • Enhancement | Add more ethnicities

Bug fixes:

  • Bug Fix | Display chr number for finalized cases in finalize tab

  • Bug Fix | Add new case | Reactivate batch mode using HPO IDs

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