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Fig. 1 | Genome Medicine

Fig. 1

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

Fig. 1

Genome coverage and sequencing depth in the down-sampled single-cell datasets. Each panel depicts a single-cell dataset (e.g., W4) where the number in the header indicates its original sequencing depth (e.g., 47×). Solid lines represent the average genome coverage (proportion of bases covered by at least one read, measured per nucleotide) obtained for the different replicates at the different down-sampled depths. Dots correspond to single cells. Shaded areas indicate the standard deviation from the mean

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