ProtVar will be launched on Wednesday 24th May at an EMBL-EBI webinar at 15:30 BST (UTC+1). We will discuss the various ways in which ProtVar can help users with their work as well as recent improvements and fixes. Places are limited so please register to secure your place here.
We have made some fixes and changes since the release on May 24th.
- novel predictions now in downloaded result files
- fixed failure of some large files due to a bug
- added a max. file limit of 10MB to cope with load
- improve foldx coverage to 208M (from 5.9M) predicted values covering all 19 possible mutations
- bug fix: ensure that GRCh37 build is correctly used in the download
- bug fix: missing fields (
Genomic_location, Cytogenetic_band, Other_identifiers_for_the_variant, Diseases_associated_with_variant) added to generated download - added optional
variantAAfilter to/foldx/{acc}/{pos}and/function/{acc}/{pos}endpoints - added direct variant link using search terms