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. 2023 Mar 16;29(3):593–604. doi: 10.1038/s41591-022-02189-0

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© The Author(s) 2023

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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Extended Data Fig. 6 — a, Visualization of 64,260 lymphoid cells following clustering and color-coded by lymphoid lineages (CD4+T, CD8+ T, innate lymphoid, B, and plasma). Visualization of CD4+ T (b; n = 17,473), CD8+ T (c, n = 27,465), and innate lymphoid cells (d, n = 9,161) following clustering and color-coded by sublineages. e, Visualization of 23,663 myeloid cells following clustering and color-coded by lineages. All right panels: Bubble plots showing mean expression and abundance of marker genes that are differentially expressed among lymphoid cells (a), lymphoid subsets (b-d), and myeloid (e) cells based on lineage or sublineage.