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. 2024 Feb 16;30(3):785–796. doi: 10.1038/s41591-024-02803-3

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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 — Panel (A) shows, for each microbial SGB listed, its slopes in patients with PFS ≥ 12 months and PFS < 12 months on monotherapy, respectively. Red and blue colors indicate whether the focal SGB is increasing or decreasing in its abundance over study visits, respectively. It then shows the average difference between patients with PFS ≥ 12 and PFS < 12 months across the different study visits. Non-gray cells in the heatmap correspond to the focal SGB’s log-fold change in abundance between patients with PFS ≥ 12 and PFS < 12 months, respectively. Teal cells correspond to study visits for which the abundance of the focal SGB is higher in in patients with PFS ≥ 12 than with PFS < 12 months on monotherapy, and vice versa for brown cells (at 90% BCL). Gray cells denote differences between patients with PFS ≥ 12 and PFS < 12 months on monotherapy whose 90% CI overlapped with zero.