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Figure 1 | Genome Medicine

Figure 1

From: Cell-lineage heterogeneity and driver mutation recurrence in pre-invasive breast neoplasia

Figure 1

Variant allele frequencies from the six patients. Each SNV by sample combination is represented by a point, colored blue if it was called present in a sample, or orange if it was called absent. The 0.02 VAF cutoff used to determine presence or absence for most variants is shown as a dashed horizontal line. Means and standard deviations are shown, which are so close in the absent classes that they appear as a single horizontal line.

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