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. 2021 Aug 19;158:30. doi: 10.1186/s41065-021-00193-x

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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. 5 — A The difference of enrichment scores of 28 immune cells in each subtype in the TCGA-GBM Agilent cohort. B The enrichment scores of immune cells with a significant difference in the good and poor prognosis subtypes in the TCGA-GBM Agilent cohort. C The difference of enrichment scores of 28 immune cells in each subtype in the TCGA-GBM HiSeq cohort. D The enrichment scores of immune cells with a significant difference in the good and poor prognosis subtypes in the TCGA-GBM HiSeq cohort. E The intersection of four immune molecular subtypes with the previous five molecular subtypes. F The distribution of four immune subtypes in 56 immune-related features; 11 immune features presented FDR < 0.05