Fig. 1From: FiNGS: high quality somatic mutations using filters for next generation sequencingThe FiNGS workflow. A user supplies the BAM files from a pair of matched normal and tumor samples, along with a standard VCF file listing somatic mutations and a text file detailing the filters and thresholds to be used. FiNGS outputs a filtered VCF file, along with a number of additional files that the user may find usefulBack to article page