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

Genome Res · 2023 · PMC10760445 · PMID 37993137

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a clear trendno p-value reported
SCsnvcna's pairwise SNV error and pairwise SNV/CNA error did not show a clear trend, whereas the pairwise SNV error was around 0.2 and pairwise SNV/CNA error was around 0.25.

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