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. 2023 Apr 10;20(5):695–705. doi: 10.1038/s41592-023-01829-8

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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. 7 — a, Visualization of all the amplicons in representative cells (combined, left) and separated by gene clusters (right) across pulse-chase timepoints. Scale bar: 10 µm. Colors of amplicons indicate unique gene clusters. b, Boxplots showing the subcellular distribution of RNA reads over time in each kinetic cluster. Vertical lines indicate s.d. For each cluster, 0, 2, 4, 6 hrs chase have n = 1028, 910, 946, 542 cells, respectively.