Integrating SNVs and CNAs on a phylogenetic tree from single-cell DNA sequencing data

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Figure 2.
Figure 2.

Group 1: evaluation of methods given varying sequencing errors. Genotype error, pairwise SNV error, and pairwise SNV/CNA error are shown for SCsnvcna, SCARLET, COMPASS, SiFit, SCG, RobustClone, and SiCloneFit on varying FP rate (A), varying FN rate (B), and varying missing rate (C).

This Article

  1. Published in Advance November 22, 2023, doi: 10.1101/gr.277249.122 Genome Res. 33: 2002-2017

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