Figure 1From: Identification of somatic mutations in cancer through Bayesian-based analysis of sequenced genome pairsPerformance of Seurat’s somatic point mutation detection with varying genomic coverage. Legend: The sensitivity ( A ) and false discovery rate ( B ) for Seurat’s somatic point mutation detection method, evaluated on simulated cancer genome data with no simulated normal tissue contamination. Each series represents the coverage used for the ‘normal’ genome data set, and the x-axis represents the ‘tumor’ genome average coverage.Back to article page