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. 2022 May 13;13:880387. doi: 10.3389/fgene.2022.880387

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Copyright © 2022 Dai, Wen, Wu, Wu, Lv, Yan, Liu, Wang and Zheng.

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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Gene enrichment analysis for AAM-related lncRNAs based on TCGA in the high (A) and low (B) BRCA risk groups. Correlation between the TMB and the two risk subsets (C). Association between the TMB and risk score (D). Prominently mutated genes in the patients with BRCA in the different risk subgroups. The mutated genes (rows, top 20) are ranked according to mutation rate; samples (columns) are arranged to emphasize the mutual exclusivity among mutations. The right panels depicts the mutation percentage, and the top panel indicates the overall number of mutations. The color coding indicates the mutation type (E).