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. 2020 Jan 3;11:69. doi: 10.1038/s41467-019-13803-0

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© The Author(s) 2020

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. 4 — a Copy-number changes in breast cancer (amplification of oncogenes in red and deletion of tumor suppressors in blue) identified according to criteria described in the Methods section. The orange line represents the significance threshold (FDR = 0.25). The complete list of chromosome location peaks associated to cancer driver genes in Pan-Cancer study is included in Supplementary Data 8. b Boxplot showing log2 (intron mutation counts), c log2 (missense mutation counts) for tumor suppressor and oncogenes detected in Pan-Cancer study, and d breast cancer log2 (mutation type count).