Closed ywzhang071394 closed 2 months ago
Quite a number of variants in your 28k calls are germline, do you have any PoNs for filtering the calls?
We used the default PoNs, which is embedded in the ClairS-TO package.
You might want to find or construct a PoN that is specific to your cancer type or population to further reduce the number of variants.
Hi, I am using Clairs-TO to call somatic small variant from PacBio Revio tumor data. As a result, ClairS-TO detected ~28000 variants, which is much larger than I expected. I am not sure whether there are many false positive and thus post this issue to enquire if it's normal condition when using ClairS-TO.
Thanks!