| 이름 | 설명 |
|---|---|
| SNVReviewer | The SNV reviewer takes as input a .vcf file (from the normal sample) and a .bam file (from the paired tumor sample). It processes a particular chromosome at a time. For all variants in the .vcf file that pass our filters, we review the variant allele frequency in the .bam file from the tumor sample. We output that data in tabular format. |
