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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