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. 2021 Mar;9(6):500. doi: 10.21037/atm-21-927

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2021 Annals of Translational Medicine. All rights reserved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0.

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Molecular characteristics of patients in the high- and low-risk groups. (A) Gene set enrichment analysis of the top five pathways significantly enriched in the high-risk group. (B) Gene set enrichment analysis of the top five pathways significantly enriched in the low-risk group. (C) Significantly mutated genes (SMGs) in HCC patients in the high- and low-risk groups. The mutated genes are sorted by mutation rate (row, top 10). The samples are arranged to highlight the mutual exclusivity between mutations. The percentage of mutations is shown on the right, and the total number of mutations is shown on the top. Color coding indicates the type of mutation.