Closed Tinalxt closed 7 years ago
I also have this question
Yes, that is possible. You need to run SiNVICT separately on the tumor and normal sample. Afterwards, you should subtract the mutations which were also detected in the normal sample from the set of variants called in the tumor sample.
Hi~ I wonder if SiNVICT can call the somatic mutation? Such as a pair of tumor-nomal sample.