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. 2022 Apr 4;2022(2):hoac016. doi: 10.1093/hropen/hoac016

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© The Author(s) 2022. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 3. — Functional enrichment analysis of the endometrial receptivity genes within the meta-analysed transcripts. The most representative items detected were consistently dysregulated in the intersection between each endometrial receptivity test and the studies included in the meta-analysis (endometrial receptivity array (ERA) versus studies; ER Map^®/ER Grade^® test versus studies; and beREADY^® test versus studies). Only the processes that have a significant false discovery rate (FDR) across the three comparisons are shown. The values of FDR in the figure correspond to the average value of the FDR for each comparison. Complete details of the results of the meta-analysis are described in Supplementary Table SV. BP, biological processes; CC, cellular components; MF, molecular functions.