Closed malachig closed 4 years ago
For 1. I would recommend CIViCpy over parsing our TSVs.
For 4. and 5. we would need to figure out how to associate their variants with ours. I would recommend using the ClinGen Allele Registry as an in between since users are already able to look up CIViC variants by CAID.
I would suggest that representation of CIViC EIDs in ProteinPaint be restricted to accepted status. some details like if an EID has is flagged might also be taken into account, but the main issue would be restricting to accepted.
If we want to do this we should instruct Xin to import/parse the accepted VCF instead of the accepted and submitted one.
Hmmm, right now you won't see too much detail about the evidence associated with each variant until you follow the link which takes you back to CIViC. There you would see the status and warnings.
Since we are not conveying any claims about the evidence in ProteinPaint maybe this is okay.
Our current default view of variants when you go to a gene in CIViC is "Show variants with accepted and/or submitted evidence".
I think we should mirror that behavior otherwise it will be confusing as one goes back and forth between a gene view in CIViC and gene view in ProteinPaint.
I also like this approach because it conveys all the variants that CIViC has some info on, but you go back to CIViC for the full details.
The statuses are being outputted in the CSQ field so if they aren’t currently being displayed in protein paint it would be easy to add.
It seems that if the links are at the variant level then there should be no problem.
We are working with ProteinPaint to have gene and variant level cross linking. After preliminary discussion with Dr. Zhang and members of her team the following action items were proposed:
Other notes: