Scout user meeting 6/9

[henrikstranneheim]

• Blog post 3.3
• https://github.com/Clinical-Genomics/scout/issues/587
• https://github.com/Clinical-Genomics/scout/issues/588

Coming up 3.4:

• Pin, mark https://github.com/Clinical-Genomics/scout/issues/559
• New SV annotations https://github.com/Clinical-Genomics/scout/issues/557
• Aggregate view https://github.com/Clinical-Genomics/scout/issues/320

Information points

• Reruns
• Hardware purchases

Discussion points

• Genes "lacking" transcripts https://github.com/Clinical-Genomics/scout/issues/570
• ACMG auto https://github.com/Clinical-Genomics/scout/issues/582
• Clinical filter https://github.com/Clinical-Genomics/scout/issues/577
• SNV/SV overlap https://github.com/Clinical-Genomics/scout/issues/567
• Nordic variant sharing workshop (Nov 16-17 in Oslo)
• SV training / workshop / discussion within community (2nd week of November)
• Future development projects - Discussion
  • SV Scout view
  • Aggregate statistics in Scout
  • Clinical Report feature in Scout
  • Clinical data sharing
  • WTS (Whole Transcriptome Sequencing)

[vwirta]

Made some additions

[robinandeer]

New issues:

"Sanger email for SV": https://github.com/Clinical-Genomics/scout/issues/597

[robinandeer]

• [ ] Show on variant if a gene doesn't have an NM transcript