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. Author manuscript; available in PMC: 2020 Aug 10.
Published in final edited form as: Nat Biotechnol. 2020 Feb 10;38(4):433–438. doi: 10.1038/s41587-020-0407-5

Figure 2 -. Single Nucleotide Variants.

Figure 2 -

(A) Plot of sensitivity versus coverage using four tools to call single nucleotide variants from enrichment data in GM12878 for a 140kb region containing 174 annotated SNVs (B) Visual representation of high-confidence variants detected by nanopolish in the MinION data from GM12878 for the captured region around TP53, reads phased into homologous alleles using WhatsHap. (C) High-confidence variants identified in primary tissue from a tumor/normal pair, red arrows used to demarcate tumor-specific variants.