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. 2024 Mar 21;25(4):703–715. doi: 10.1038/s41590-024-01782-4

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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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Extended Data Fig. 8 — a, Projected UMAP of 242,832 healthy bone marrow mononuclear cells (10x Genomics Chromium platform) from the aggregate of three prior studies to our CITE-Seq fully titrated bone marrow reference. The reference CITE-Seq clusters used for label transfer and UMAP coordinate projection are shown in the inset. b, Bone marrow cell frequencies of all unsorted cells from 38 healthy donors. c, UMAP of unsupervised clustering (ICGS2) of cells from 20 bone marrow healthy donors (GSE120221). d, Projection of CITE-Seq label mapping scores from the software cellHarmony in the UMAP from panel c to infer annotation confidence.