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. 2018 Feb 12;9(2):213. doi: 10.1038/s41419-017-0242-x

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© The Author(s) 2018

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. 7 — Many of the differentially expressed genes demonstrated strong prognostic value for patient survivals. Some of the genes are known associated with tumorigenesis (e.g., Fas and Id3) while others (e.g., Ankle2, Zmynd11, and Tgm2) have not been previously reported in cancers and/or GBM. Nonetheless, the known functions of these genes are highly suggestive for their potential roles in brain tumors. For each DEG, the 152 patients were arbitrarily divided as 76 patients with high expression versus 76 patients with low expression