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. 2020 Dec 14;21(Suppl 17):484. doi: 10.1186/s12859-020-03782-1

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© The Author(s) 2020

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. 2 — Discrimination of CD8⁺ T cell epitopes by immunoproteasome cleavage predictions considering HLA I restriction. Figure shows the accuracy (ACC) of C-terminus immunoproteasome cleavage predictions discriminating virus-specific CD8⁺ T cell epitopes restricted by specific HLA I molecules (columns) from 9-mer peptides, selected randomly from the same source proteins than the epitopes. The analysis was carried out using PCPS immunoproteasome model at a threshold of 0.5 and the represented ACC corresponds to means ± SD obtained after repeating the analysis five times with different random 9-mer peptides