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. 2021 Sep 30;44(2):699–717. doi: 10.1007/s11357-021-00466-3

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© The Author(s) 2021

Open AccessThis 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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Fig. 4 — Multi-tissue vervet clock applied to 16 tissue types from humans. Each dot corresponds to a human tissue samples. The predicted DNAm age in human tissues according to the vervet multi-tissue clock (y-axis) and chronological age of the human specimens (x-axis). The number of samples is shown in parentheses; cor, Pearson’s correlation; MAE, median absolute error