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Fig. 2 | Genome Medicine

Fig. 2

From: Sensitivity to sequencing depth in single-cell cancer genomics

Fig. 2

SNV recall and precision in single-cells. a Barplots illustrating the proportion of bulk germline variants called in the single-cell down-sampled datasets (germline recall). b Proportion of bulk somatic variants identified in the single-cell down-sampled datasets (somatic recall). c Proportion of somatic variants called in the down-sampled datasets that were also identified in the original single-cell dataset (somatic precision). Error bars indicate 95% confidence intervals. Numbers above bars indicate number of calls (for b and c these numbers are the same)

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