Måns Magnusson
Måns Magnusson
We should have a gemini database with "synthetic" variants so we always know what to expect when writing tests
We should think of a solution for how to do searches for all variants in all cases. When using the gemini- and mongo adapters this will be straightforward, we just...
You know what to do @robinandeer ...
This would create a way to narrow the analysis to custom regions
Creating this issue to gather similar issues in one. In general we need suggestions of how to pick these from the vcf, what are the common named keys, are they...
One should be able to point to a chanjo database and get chanjo reports from the case/individual/variant view
These will not have any RefSeq defs. See https://github.com/Clinical-Genomics/scout/issues/644 - [ ] export MT exons/transcripts from Scout @moonso - [ ] update prod chanjo4 database - [ ] update pipeline...