Open wenweixiong opened 3 years ago
Hello, souporcell only contains germline variants which may consist of both SNP and SNV. Let's assumed that your batch contains normal and cancer samples from an individual. From the comparison between normal and cancer, you might get SNVs. When you find specific the SNV loci in the souporcell.vcf, it will be helpful to identify which souporcell cluster is cancer sample. good luck!
I'm interested in tracing previously identified somatic mutation for each single cell. am wondering if the souporcell_merged_sorted_vcf.vcf.gz contains only germline variants or it also contains somatic variants? If the vcf only contains germline variants, how may I tweak the pipeline to also call somatic variants?