| Literature DB >> 29842781 |
Travis W Murphy, Yuan-Pang Hsieh, Sai Ma, Yan Zhu, Chang Lu.
Abstract
Genome-wide epigenetic changes, such as histone modifications, form a critical layer of gene regulations and have been implicated in a number of different disorders such as cancer and inflammation. Progress has been made to decrease the input required by gold-standard genome-wide profiling tools like chromatin immunoprecipitation followed by sequencing (i.e., ChIP-seq) to allow scarce primary tissues of a specific type from patients and lab animals to be tested. However, there has been practically no effort to rapidly increase the throughput of these low-input tools. In this report, we demonstrate LIFE-ChIP-seq (low-input fluidized-bed enabled chromatin immunoprecipitation followed by sequencing), an automated and high-throughput microfluidic platform capable of running multiple sets of ChIP assays on multiple histone marks in as little as 1 h with as few as 50 cells per assay. Our technology will enable testing of a large number of samples and replicates with low-abundance primary samples in the context of precision medicine.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29842781 PMCID: PMC6019315 DOI: 10.1021/acs.analchem.8b01541
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986