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. 2021 Feb 23;9:54. doi: 10.1186/s40168-020-00986-8

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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/. 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. 7 — No influence of genetics on mother-child distances for individual species. Violin plots comparing the distribution of mother-child dissimilarities in the biologic and adoptive groups. For the 10 most abundant species, Bray-Curtis dissimilarities were generated based on presence/absence of strains for each species. Mother-child distances (dissimilarities) were not significantly different between the adoptive and biologic groups for any species. Wilcoxon rank sum test was used for statistical comparisons, and p values generated were corrected for false positives (Benjamini-Hochberg procedure) to generate q values shown. The 50th quantile of each distribution is marked for comparison. Data is based on the saliva/soft tissue swab samples