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. 2024 Jan 3;27(1):137–147. doi: 10.1038/s41593-023-01510-5

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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 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. 5 — Mean population average of all non-targeted cells in response to each 10 cell ensemble stimulation (gray dot). Average ± SEM for each recording FOV in red. Divided by expression selectivity driver (Emx-cre, CamK2-tTA, or SepW1-Cre) and viral construct (Syn-DIO-ChroME, Tre-ChroME, Tre-ChroME2s, or CAG DIO-ChroME2s). Sex of each mouse is noted below. Note SepW1-Cre ensembles are more likely to be spread out, due to the sparse nature. Each dot is the mean response to an ensemble across all conditions N = 160 Ensembles, 18 FOVs, 13 mice.