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. 2022 Sep 24;13:5614. doi: 10.1038/s41467-022-33210-2

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Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — Prospectively collected genetic data on fusions from all cancer patients, and mutational data from patients with non-small cell lung cancer (NSCLC; detected by OncoPanel at Dana Farber Cancer Institute) were combined. Unique fusions identified in patients with EGFR L858R or deletion in exon 19 (del19) were classified into five groups.