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Whats new in 3.4?

What's new in 3.4?

Posted: 19 Sep 2017

Time for a new update - this time without any major changes

New features

  • Aggregate dashboard: view global statistics like how many cases have been solved in Scout?
  • Pin and mark SV variants, thanks @dnil!
  • Gene view: information is now displayed for both build GRCh37 and GRCh38
  • you can now filter genes by HGNC id as well as HGNC symbol
  • new popup with variant comments, thanks @dnil!
  • we now store more information about previous analyses for every case like delivery report
  • the gene panel update function has been improved and the documentation is also up-to-date!


  • worked to improve the documentation in general
  • fixed issue that made commenting on a variant fail
  • cases will now change status from "solved" when unmarking causative
  • fixed a bug with the ClinSig filter, thanks @dnil!
  • the order of ACMG classification and criteria is now correct
  • you can now toggle a selected ACMG classification on/off
  • the OMIM inheritance concordance is now fixed