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. 2022 Apr 28;7:30. doi: 10.1038/s41525-022-00300-5

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — Nucleosome scores (a) and genome-wide z-scores (b) are shown for 130 patients with benign ovarian disease, 141 patients with borderline and invasive carcinoma (including 8 patients with metastases) combined, 41 patients with borderline ovarian tumors (BOT), 100 patients with invasive ovarian carcinoma (including 8 patients with metastases), 62 patients with HGSOC, 30 patients with non-HGSOC, and 8 patients with adnexal metastases of other primary cancers. Every case is indicated by a blue dot and HGSOC cases are highlighted in red. The axis of the genome-wide z-scores was truncated for visualization purposes. ***p-value < 0.001; *p-value < 0.05 (Mann–Whitney). Further descriptive statistics are detailed in Supplementary Tables 2 and 3.