Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 Oct 21;61:103076. doi: 10.1016/j.ebiom.2020.103076

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2020 The Author(s)

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

PMC Copyright notice

Fig 2 — Removal of the parental effects in neonatal DMRs. (a) Violin-box plots displayed the distribution of DNA methylation level in paternal samples at hyper- (upper) and hypo-DMRs (lower) of the seven comparisons, IVF-ET versus CTRL, ICSI-ET versus CTRL, IVF-FET versus CTRL, ICSI-FET versus CTRL, ICSI-ET versus IVF-ET, IVF-FET versus IVF-ET, and ICSI-FET versus IVF-ET neonatal samples. The p-value between two groups was determined by Wilcoxon rank-sum test. (b) Bar graph showed the proportion of DMRs with/without hereditary effects in the hyper- or hypo-DMRs of each comparison. Any one of the 14 groups of DMRs were classified into four subgroups, without hereditary effects (w/o), only with paternal hereditary effects (w/paternal, only overlapped with the DMRs of comparison for the corresponding fathers), only with maternal hereditary effects (w/ maternal, only overlapped with the DMRs of comparison for the corresponding mothers), and with biparental hereditary effects (w/ biparental, overlapped with the DMRs of comparisons for the corresponding fathers and mothers).