C. Cerutti, S. Leroux, P. Terzian, D. Gourichon, Joanna Lledo, C. Iampietro, J. Sabban, Caroline Vernette, C. Klopp, C. Donnadieu, G. Devailly, Frédérique Pitel, C. Vandecasteele
2026.6.5Scientific Data
Abstract
Whole Genome Bisulfite Sequencing (WGBS) has been the gold standard DNA methylation mapping and quantification for over a decade. Oxford Nanopore Technologies (ONT) sequencing directly measures nucleotide modifications. In this study, we have compared DNA methylation levels (5-methylcytosine) at CpG sites in the quail genome using WGBS and ONT. Samples were collected to investigate transgenerational DNA methylation changes in Japanese quail following ancestral exposure to a phytoestrogen. Blood samples from 24 third-generation (G3) individuals—descendants of either treated or untreated ancestors—were sequenced after bisulfite conversion. Both methods revealed broadly consistent methylation patterns. ONT reads covered more CpG sites and detected a higher number of differentially methylated cytosines (DMCs). Principal component analyses showed that both sex and ancestral treatment groups accounted for a portion of the observed epigenetic variation, for both technologies. Strong concordance between WGBS and ONT results supports the reliability of ONT sequencing for epigenomic research, including in quails. These data pave the way for further investigation into whether genistein induces epigenetic changes for several generations.
Citation format
CERUTTI, C., et al. DNA methylation profiles of quail blood cells by whole-genome bisulfite and oxford nanopore sequencing. Scientific Data, 2026.