Entering edit mode
3.2 years ago
vpsev3
▴
20
Hello,
I'm desperately trying to match my genome with ClinVar, I've been on it for several hours but nothing is working
Now I have found this software which looks good https://github.com/brentp/slivar
But I don't understand anything about the parameters, I have my genome in vcf.gz and the ClinVar database in the same format aligned with the GRCh38, I would like to find variants referenced as "pathogenic" or "likely pathogenic"
Can you help me ?
Thank you.
