| Literature DB >> 36173565 |
Shinjiro Hino1, Tetsuya Sato2, Mitsuyoshi Nakao3.
Abstract
Chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq) is the most widely used method for analyzing genome-wide DNA-protein interactions. Because there is considerable variation in the modes and strengths of DNA-protein interactions, chromatin immunoprecipitation (ChIP) protocols have been diversified and optimized for different needs. Here, we describe protocols for detecting histone modifications and modifiers using various crosslinking and immunoprecipitation conditions. We provide a complete ChIP-seq workflow covering sample preparation, immunoprecipitation, next-generation sequencing (NGS) library preparation, and data analyses.Entities:
Keywords: Dual crosslink; Histone; Immunoprecipitation; Next-generation sequencing
Mesh:
Substances:
Year: 2023 PMID: 36173565 DOI: 10.1007/978-1-0716-2724-2_4
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745