| Literature DB >> 29956160 |
Diana Youhanna Jankeel1, Justin Cayford1, Benjamin Joachim Schmiedel1, Pandurangan Vijayanand1,2, Grégory Seumois3.
Abstract
Chromatin immunoprecipitation followed by sequencing (ChIP-Seq) is the preferred approach to map histone modifications and identify cis-regulatory DNA elements throughout the genome. Multiple methods have been described to increase the efficiency of library preparation and to reduce hands-on time as well as costs. This review describes detailed steps to perform cell fixation, chromatin shearing, immunoprecipitation, and sequencing library preparation for a batch of 48-96 samples with small cell numbers. The protocol implements a semiautomated platform to reduce technical variability and improve signal-to-noise ratio as well as reduce hands-on time, thus allowing large-scale epigenetic studies of clinical samples with limited cell numbers.Entities:
Keywords: ChIP-Seq; H3K27ac; IP-Star; Tagmentation
Mesh:
Substances:
Year: 2018 PMID: 29956160 PMCID: PMC6844362 DOI: 10.1007/978-1-4939-7896-0_22
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745