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. 2022 May 19;606(7913):389–395. doi: 10.1038/s41586-022-04735-9

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© The Author(s) 2022

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 — a, Shannon entropy (S, left), and the difference in Shannon entropy between recurrent (S_rec) and primary (S_prim) PDACs (right). b, TMB and neoantigen number (NA) in primary and recurrent PDACs. c, d, The difference in TMB and NA (c), and the number of mutations that generate neoantigens (NA Mut) (d) between recurrent and primary PDACs. n indicates the number of individual tumours. The horizontal bars show the median values. For a–d, P values were determined using two-tailed Mann–Whitney U-tests.

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