Mundade, RasikaOzer, Hatice GulcinWei, HanPrabhu, LakshmiLu, Tao2016-10-202016-10-202014Mundade, R., Ozer, H. G., Wei, H., Prabhu, L., & Lu, T. (2014). Role of ChIP-seq in the discovery of transcription factor binding sites, differential gene regulation mechanism, epigenetic marks and beyond. Cell Cycle, 13(18), 2847–2852. http://doi.org/10.4161/15384101.2014.9492011551-4005https://hdl.handle.net/1805/11209Many biologically significant processes, such as cell differentiation and cell cycle progression, gene transcription and DNA replication, chromosome stability and epigenetic silencing etc. depend on the crucial interactions between cellular proteins and DNA. Chromatin immunoprecipitation (ChIP) is an important experimental technique for studying interactions between specific proteins and DNA in the cell and determining their localization on a specific genomic locus. In recent years, the combination of ChIP with second generation DNA-sequencing technology (ChIP-seq) allows precise genomic functional assay. This review addresses the important applications of ChIP-seq with an emphasis on its role in genome-wide mapping of transcription factor binding sites, the revelation of underlying molecular mechanisms of differential gene regulation that are governed by specific transcription factors, and the identification of epigenetic marks. Furthermore, we also describe the ChIP-seq data analysis workflow and a perspective for the exciting potential advancement of ChIP-seq technology in the future.en-USAttribution-NonCommercial 3.0 United StatesChromatin ImmunoprecipitationmethodsEpigenesis, GeneticGene Expression ProfilingSequence Analysis, DNATranscription FactorsmetabolismArticle