Skip to main content
. 2023 Jul 27;55(8):1301–1310. doi: 10.1038/s41588-023-01446-3

Extended Data Fig. 2. Analyses of single molecule sequence changes in PCAWG lung cancer and normal samples.

Extended Data Fig. 2

a, Single molecule mutation frequencies in Pan-Cancer Analysis of Whole Genomes (PCAWG) lung cancers (n = 31) and blood derived matched normal samples (n = 31). Adjusted p-values (padj) were generated using the two-sided Wilcoxon rank sum test and were corrected for multiple comparisons using the Benjamini-Hochberg method. The horizontal dashed line indicates a p-value of 0.05. b, Cross-validated regional differences in single molecule mutation frequencies in PCAWG lung cancers (n = 31) and blood derived matched normal samples (n = 31), median-centered within each mutation type. Adjusted p-values were generated using the two-sided Wilcoxon rank sum test and were corrected for multiple comparisons using the Benjamini-Hochberg method. The horizontal dashed line indicates a p-value of 0.05. All boxplots represent the interquartile range with whiskers drawn to the highest value within the upper and lower fences (upper fence = 0.75 quantile + 1.5 × interquartile range; lower fence = 0.25 quantile – 1.5 × interquartile range). The solid middle line in the boxplot corresponds to the median value.