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. 2020 May 8;10:726. doi: 10.3389/fonc.2020.00726

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Copyright © 2020 Liu, Huang, Liu, He, Zhao, Yang, Long, Zong, Zeng, Liu, Liao, Duan, Gong and Chen.

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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Mutational profiles of ALK positive NSCLC patients. (A) This is the oncoprint of the somatic SNVs and Indels in 34 patients in our study. Somatic alterations included missense, nonsense, frameshift indel, in-frame indel, splice site, translation start site, multi_Hit mutations. The genes are ranked by the frequency of the mutations across all samples. (B) This is the oncoprint of the somatic SNVs and Indels in 34 patients from the MSK-IMPACT study. Somatic alterations included missense, nonsense, frameshift indel, in-frame indel, and splice-site mutations. The genes are ranked by the frequency of the mutations across all samples.