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. 2020 Jul 23;8:642. doi: 10.3389/fcell.2020.00642

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Copyright © 2020 Tu, Wu, Wang, Hu, Tao, Li, Huang and Zhu.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Functional analysis of 2571 differentially expressed genes (DEGs) between the low- and high-risk subgroups. (A) Heatmap of enriched terms across the inputted gene list, colored according to p-value. Network of enriched terms colored according to (B) cluster ID (nodes with the same cluster ID are typically close to each other) and (C) p-value (terms with more genes tend to have higher p-values). (D) Gene set enrichment analysis (GSEA) indicating that tumor hallmarks were enriched in the high-risk subgroup.