Skip to main content
. 2018 Nov;20(6):822–835. doi: 10.1016/j.jmoldx.2018.06.007

Figure 3.

Figure 3

Whole-genome sequencing coverage. A: Representation of the coverage (mean and SD) for all variants in cancer census genes based on our validation sample data. Red filled circles indicate mean coverage of genes in our validation sample set. Black lines indicate SD limits from mean. Mean coverage per gene when targeting 80× is shown. B: Percentage of genome sequencing coverage for all 64 samples at 30× read depth (PCT_30X) and 40× read depth (PCT_40X). FF, fresh or frozen; FFPE, formalin-fixed, paraffin-embedded.