Release 4.11

[4.11.0]

Added

• Display locus name on STR variant page
• Alternative key GNOMADAF_popmax for Gnomad popmax allele frequency
• Automatic suggestions on how to improve the code on Pull Requests
• Parse GERP, phastCons and phyloP annotations from vep annotated CSQ fields
• Avoid flickering comment popovers in variant list
• Parse REVEL score from vep annotated CSQ fields
• Allow users to modify general institute settings
• Optionally format code automatically on commit
• Adds command to backup vital parts scout export database
• Parsing and displaying cancer SV variants from Manta annotated VCF files
• Dismiss cancer snv variants with cancer-specific options
• Add IGV.js UPD, RHO and TIDDIT coverage wig tracks.

Fixed

• Slightly darker page background
• Fixed an issued with parsed conservation values from CSQ
• Clinvar submissions accessible to all users of an institute
• Header toolbar when on Clinvar page now shows institute name correctly
• Case should not always inactivate upon update
• Show dismissed snv cancer variants as grey on the cancer variants page
• Improved style of mappability link and local observations on variant page
• Convert all the GET requests to the igv view to POST request
• Error when updating gene panels using a file containing BOM chars
• Add/replace gene radio button not working in gene panels