Additional file 3: of Identification of single nucleotide variants using position-specific error estimation in deep sequencing data KleftogiannisDimitrios PuntaMarco JayaramAnuradha SandhuShahneen WongStephen Gasi TandefeltDelila ConteducaVincenza WetterskogDaniel AttardGerhardt LiseStefano 2019 Figure S2. Fraction of sites in a normal sample sequenced at a given coverage or more across our custom AmpliSeq panel. The values are calculated over 30 randomly selected samples. (PPTX 59 kb)