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. 2022 Sep 20;13:5511. doi: 10.1038/s41467-022-33052-y

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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. 3 — a UMAP-plot of the subclustering of 18,082 cells from tumoral (n = 9) and matched peri-tumoral (n = 8) BC samples (TME and pTME respectively, composed of all cell types). b Heatmap of the expression levels of the top-10 marker genes in all 27 stromal subclusters derived from the non-EC enriched dataset (composed of all cell types). Color scale: red – high expression, blue – low expression. EC endothelial cell, DC dendritic cell, NK natural killer. c UMAP-plot of the same cells as in a, color-coded for the 12 major cell types.