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. 2023 Sep 29;23:273. doi: 10.1186/s12866-023-03012-7

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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 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — Significant differences in ASV abundance across the epidermis was analysed using mixed linear modelling (AD patients and healthy participants visualised together). A heat tree was constructed from the 238 ASVs that were found to significantly vary between tapes, with node size representing the total number of ASVs (q-value > 0.05) and node colour representing the change in ASV abundance (log₂) between the swabs (higher relative abundance in swabs represented by blue coloration) and the tape-35 samples (higher relative abundance in tape 35 represented by green coloration)