Additional file 2: of Identification of single nucleotide variants using position-specific error estimation in deep sequencing data

Figure S1. Variant allele frequency (VAF) distributions for the A, T, C, G nucleotides as calculated from 30 randomly chosen normal samples across our custom AmpliSeq panel. Only VAFs < 60% are displayed. The red lines mark VAF = 20%. (PPTX 278 kb)