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 <â60% are displayed. The red lines mark VAFâ=â20%. (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