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Additional file 3: 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 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)

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    BMC Medical Genomics

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

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