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. 2022 Nov 18;20:531. doi: 10.1186/s12967-022-03723-x

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© The Author(s) 2022

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. 3 — Pseudotime analysis of Neutrophils and mutational analysis of NDRGs. According to the pseudotime (A) of Neutrophils, the cell population was divided into four different differentiation states (B), and NDRGs (G) were obtained by difference analysis of differentiation states. GSVA (KEGG terms) analyzes four different differentiation states (C–F). Top 30% mutation frequency of NDRGs and mutation type (H) and mutation status of NDRGs in different states (I)