Additional file 2: of Identification of single nucleotide variants using position-specific error estimation in deep sequencing data Dimitrios Kleftogiannis Marco Punta Anuradha Jayaram Shahneen Sandhu Stephen Wong Delila Gasi Tandefelt Vincenza Conteduca Daniel Wetterskog Gerhardt Attard Stefano Lise 10.6084/m9.figshare.9247331.v1 https://springernature.figshare.com/articles/presentation/Additional_file_2_of_Identification_of_single_nucleotide_variants_using_position-specific_error_estimation_in_deep_sequencing_data/9247331 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) 2019-08-03 05:00:00 Next generation sequencing (NGS) Cancer genomics Variant calling Deep sequencing Targeted sequencing Ion torrent Liquid biopsies Error correction