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. 2021 May 5;13:104. doi: 10.1186/s13148-021-01091-9

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — Verification of the 8 methylated markers in the GEO datasets. a A hierarchical cluster heatmap shows the methylation intensity of the 8 markers in databases of PCNSL and 11 other CNS tumors downloaded from the GEO database. b The table presents the methylation characteristics and performance of each of the 8 markers to distinguish PCNSL from the 11 other CNS tumor samples. N number of samples, AUC area under the curve, CI confidence interval, P Mann–Whitney statistics, PCNSL primary central nervous system diffuse large B-cell lymphoma, CNS central nervous system