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. 2021 Mar 23;141(6):959–970. doi: 10.1007/s00401-021-02300-8

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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/.

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Fig. 1 — Clinical data, histology and DNA methylation profiles. a Age distribution across histological subgroups. b Percentage of areas with subependymoma and ependymoma differentiation in mixed tumors. c Unsupervised t-SNE analysis of all 50 PFSE plus 4 spatially sampled mixed tumors together with 2801 samples comprising 82 distinct molecular CNS tumor entities. Established ependymal tumor subgroups are indicated in red