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. 2020 Oct 27;11:5417. doi: 10.1038/s41467-020-19279-7

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© The Author(s) 2020

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — a Distribution of hypomet (n = 4006) and PMA (n = 53) CGI promoter DNAme levels in embryonic day 3.5 C57 × DBA F1 ICM, androgenetic blastocysts and parthenogenetic blastocysts. Boxplots elements are as defined in Fig. 1g. Outliers not shown. Two-sided t-tests assuming unequal variances were performed. b Screenshot of the Gdap2/Wdr3 CGI promoter, presented as in Fig. 1. c, d 2D scatterplots depicting DNAme levels over individual CGI promoters in E3.5 c parthenogenetic blastocysts versus GV oocyte (data excludes polar bodies; n = 13,208) and d androgenetic blastocysts versus sperm (n = 12,225). Promoters that gain ≥20% DNAme are highlighted and genes previously identified using our allele-specific DNAme analysis pipeline are underlined. e Screenshots of the Tuba3a, Bpi and Thy1 CGI promoters. Source data are provided as a Source Data file.