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Release NotesΒΆ

Release 5.0.0

Updates

  • Case statuses are now integrated with the IP, please see Case Management for further details
  • Cancer Hotspots are available in the somatic small variant details page
  • The patient header has been condensed to maximise page space
  • Improvements to the germline BAF plot makes regions with no coverage easier to distinguish from LOH regions (e.g. resulting from UPD)
  • 8 Bug Fixes including a fix to the SV plot - arcs will now readjust on the y-axis when zooming in

Release 4.5.0

Updates

  • Germline CNVs are visible in the case summary table
  • 7 Bug Fixes

Release 4.4.0

Updates

  • Updated to use the new National Genomic Test Directory
  • Fixed link to the User Guide
  • Ability to mark variant as an artefact during Variant Interpretation
  • Moved variant list tabs to the main menu
  • 6 Bug Fixes including the population frequency round off in the variant list

Release 4.3.0

Updates

  • New case warning for unaccredited sample types
  • Colour updates for the Coverage Depth, B-allele frequency and Copy Number plots
  • Gene plots are now available in full screen mode
  • 14 Bug Fixes
Last update: 2023-10-03