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. 2023 Jun 15;29(7):1662–1670. doi: 10.1038/s41591-023-02397-2

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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. 8 — (a) snATAC-seq profiles of each nucleus colored by which donor it originated from. (b) snATAC-seq profiles colored by sub-cluster (left) and sub-cluster composition of each sample (right). (c) snATAC-seq profiles of nuclei colored by brain region (top) or sort status (bottom). (d) Quantification of accessibility in each single nucleus for selected marker genes (ArchR GeneScore). Nuclei from our samples are grouped by sub-cluster, and microglia from the Corces 2020 reference dataset, as well as C7 and C8 from Fig. 4, are included for reference.