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. 2024 Mar 28;56(4):652–662. doi: 10.1038/s41588-024-01688-9

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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/.

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Fig. 1 — A schematic highlighting the overall experimental design and the cell types we aimed to capture in the atlas. The diagram highlights the overall number of donors sequenced and how they are distributed among the various subgroups alongside the number of donor FFPE tissues that have been analyzed by multiplex immunostaining. The global UMAP representation of the final dataset is colored by general cell types captured from all 161 samples processed as part of this atlas.