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. 2021 Apr 14;14:105. doi: 10.1186/s12920-021-00952-9

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 7 — Simulation of the 990 PCAWG samples’ categorization based on their most clinically significant variant when the analysis is performed using either the 161 the 514 gene panels. The following categories were used: Tier 1 variants: patients carrying at least one Tier 1 alteration, 2C.1: patients whose most clinically significant variant is classified as 2C.1, 2C.2: patients with 2C.2 alterations, 2D: patients with 2D alterations, Tier 3: patients carrying Tier 3 alterations