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

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posted on 2019-08-03, 05:00 authored by Dimitrios Kleftogiannis, Marco Punta, Anuradha Jayaram, Shahneen Sandhu, Stephen Wong, Delila Gasi Tandefelt, Vincenza Conteduca, Daniel Wetterskog, Gerhardt Attard, Stefano Lise
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)

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    Next generation sequencing (NGS)Cancer genomicsVariant callingDeep sequencingTargeted sequencingIon torrentLiquid biopsiesError correction

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