Key New features:
Cases Page Enhancements
Persistent Filters: Filters now remain active when navigating back to the cases page. There's no need to re-select your previous settings.
Auto-Scroll: The page will automatically scroll to the last case you viewed, improving navigation and continuity.
Enhanced Table View
We've introduced additional columns to the table view for a more detailed examination:
CNV: Includes Cytoband, Copy Number, Quality, Variant Caller Name, and Family Zygosity.
SNV: Now also displays Family Zygosity, Alternate Read Count, Bayesdel value, OMIM Gene Number, and ClinVar ID.
Variant Tile Display
Quick Filters Association: Variants now show which quick filters they are associated with directly on the variant tile, streamlining the analysis process.
Case History Logging
Enhanced Event Logging: Additional events are now logged within the case history table, including any changes in the case phenotypes and case status updates.
New Filter: Internal Frequency Homozygous Count
Starting from version 73, this new filter will be available, allowing for refined searches based on the internal frequency of homozygous counts across all your cases.
These updates are designed to enhance your experience and improve the efficiency of your case analyses. We hope you find these changes beneficial and look forward to your feedback!