Fig. 4From: Genome-wide DNA methylome analysis identifies methylation signatures associated with survival and drug resistance of ovarian cancersHGSOC with high DNA methylation is usually involved in high recurrence and short overall survival (OS). a Heatmap visualization constructed using k-means clustering of differential methylation positions (DMPs: 5844) (5% false discovery rate) with at least a 20% difference in the methylation level between the platinum- sensitive and platinum-resistant groups across the 30 HGSOC cases. b Boxplot visualization of comparison of the DMP methylation levels of platinum-sensitive and platinum-resistant HGSOC. The median DMP methylation levels were 0.692 and 0.373 in platinum-resistant and platinum-sensitive cells, respectively. P value (****P < 0.0001) was computed by the Wilcoxon test. c Manhattan plot of differentially methylated positions, where each point represents the observed  − log10-adjusted P value at a CpG site. A total of 23 significant DMPs (annotated to 20 DMP-associated genes) (adjusted P < 5*10−3) found on the relevant gene promoter regions were marked. d Volcano plot showing the distribution of 5844 DMP hypermethylated DMPs (red) with FDR-adjusted P < 0.05 and difference in β value (|logFC|> 0.2). Lines represent cutoff values used to identify the most hypermethylated DMPs (red). Dashed lines represent cutoffs for the significant DMP-associated genes [1471 genes]. The most differentially regulated genes of hypermethylated sites are marked. e Boxplot visualization of comparisons of the DNA methylation levels of platinum-resistant and platinum-sensitive groups. P value (****P < 0.0001) was computed by the Wilcoxon test. f KEGG signaling pathway enrichment of differentially methylated genes analyzed by the clusterProfiler package in R. The circle size represents gene numbers, and the color represents the p-adjusted valueBack to article page