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. 2023 Nov 10;24:252. doi: 10.1186/s13059-023-03090-w

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© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 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. 1 — The genome catalog assembled from the early-life skin samples. a Schematic of study design from sampling to analysis. MAGs were constructed from single samples and pooled samples based on the two body sites of the same infant at each time point. MAGs from infant samples comprise the ELSG catalog. MAGs from mother samples were used for comparative analysis. b Completeness and contamination based on CheckM2 for each of nonredundant prokaryotic and eukaryotic MAGs included in the ELSG catalog, colored by the quality level. c Quality and completeness distribution for eukaryotic viral sequences included in the ELSG catalog