Additional file 4: of Identification of single nucleotide variants using position-specific error estimation in deep sequencing data

Figure S3. Distributions of background error values by mutation type. Panels (a), (b), (c) and (d) refers to mutations from reference allele A, C, G and T respectively. Mutations are split by alternative allele and strand, (+) and (−). Note the higher error values for A > G (T > C) and C > T (G > A) mutations. Plots are bound to error values of 0.005 on the y-axis for visual clarity. (PPTX 201 kb)