2023 Release Notes¶
Release 5.1.0¶
Release date: December 20, 2023
Updates
- Structural and copy number variants can now be filtered by size
- Structural variants can now be filtered by supporting reads e.g., a minimum number of paired or split reads
- Structural and copy number variant plots can now be moved up and down
- Link outs to resources such as MSK Impact, Genie and Mitelman Database have been added to the variant details pages for somatic small, somatic structural and somatic copy number variants
- Structural and copy number variant plot error message are now specific to the relevant visualisation
- Bug fixes including the classification options available to TINC cases
Release 5.0.0¶
Release date: November 15, 2023
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¶
Release date: September 20, 2023
Updates
- Germline CNVs are visible in the case summary table
- 7 Bug Fixes
Release 4.4.0¶
Release date: September 6, 2023
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¶
Release date: August 23, 2023
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