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Updated: Dec 27, 2025

Genome-wide Snapshot of Chromatin Regulators and States in Xenopus Embryos by ChIP-Seq
Published on: February 26, 2015
Genomics Methods for Xenopus Embryos and Tissues
Michael J Gilchrist1, Ken W Y Cho2, Gert Jan C Veenstra3
1The Francis Crick Institute, London NW1 1AT, United Kingdom; drmikegilchrist@gmail.com kwcho@uci.edu g.veenstra@science.ru.nl.
Abstract:
High-throughput sequencing methods have created exciting opportunities to explore the regulatory landscape of the entire genome. Here we introduce methods to characterize the genomic locations of bound proteins, open chromatin, and sites of DNA-DNA contact in Xenopus embryos. These methods include chromatin immunoprecipitation followed by sequencing (ChIP-seq), a combination of DNase I digestion and sequencing (DNase-seq), the assay for transposase-accessible chromatin and sequencing (ATAC-seq), and the use of proximity-based DNA ligation followed by sequencing (Hi-C).
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