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. 2024 Apr 10;25(5):2220–2238. doi: 10.1038/s44319-024-00128-3

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© The Author(s) 2024

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 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/. Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/ applies to the data associated with this article, unless otherwise stated in a credit line to the data, but does not extend to the graphical or creative elements of illustrations, charts, or figures. This waiver removes legal barriers to the re-use and mining of research data. According to standard scholarly practice, it is recommended to provide appropriate citation and attribution whenever technically possible.

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Figure EV5 — (A) The bar graph shows an equal contribution of all the splicing events toward the potential formation of tumor neoantigens reported previously (Lu et al, 2021). (B) Heat maps show HLA haplotype representation in untreated controls (Untr.). and LB-100-stimulated HT-29 human colorectal carcinoma cells from n = 3 biological replicates. (C) The plot shows the cumulative distribution of log₂ fold change in peptides presentation between LB-100-stimulated and untreated control (Untr.) HT-29 cells from n = 3 biological replicates. Highlighted in red and blue are peptides detected exclusively in LB-100 and control cells, respectively.