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. 2021 Oct 6;598(7879):214–219. doi: 10.1038/s41586-021-03220-z

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© The Author(s) 2021, corrected publication 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. 1 — a, Experimental design with lobe-based sampling and profiling. AN, ansiform lobule; COP, copula pyramidis; CUL, culmen; F, flocculus; PF, paraflocculus; PRM, paramedian lobule; SIM, simple lobule. b, UMAP visualization of 611,034 nuclei (after profile quality control and annotation; Methods), coloured by cell type identity. ODC, oligodendrocyte; OPC, oligodendrocyte precursor cell. c, Dendrogram indicating hierarchical relationships between cell subtypes (left) with a paired dot plot (right) of scaled expression (exp.) of selected marker genes for cell type identity. Background text colours correspond to cell types in b. d, Allen Brain Atlas expression staining for selected gene markers of canonical cell populations, indicating cerebellar layer localization. GCL, granule cell layer; ML, molecular layer; PCL, Purkinje cell layer.