This release improves the default filtering for germline variants on amplicon samples: we will now hide variants detected with an allelic balance under 0.2 from germline amplicon samples (they will still be allowed to pass for somatic samples).
A new algorithmic filter that filters out variants based on the number of times they have been seen in your samples.
Bugfix: Reannotating old samples now works as expected.
Bugfix: CNV analyses now have the QC report generated.
Bugfix: Fixed a display issue that could cause a mismatch between what was shown in the "VCF attributes" button and the "Filters" column of the results in specific cases.
As ever we hope you find these changes & improvements helpful, we’d love to hear any suggestions you may have, support is available as usual from firstname.lastname@example.org