ChIP-seq of H3K4me2, H3K9me2, and H3K27me3 was performed in YB5 cells to determine the impact of baseline histone methylation patterns on gene reactivation by epigenetic therapy Biological duplicates
Comprehensive identification and characterization of the binding sites of DLD-1 cells. We used ChIP-Seq method, in which next gene sequencing technology and chromatin-immunoprecipitation assay were co
H3K4me3 ChIP-seq on activated T-cell male adult (38 years) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODE_D
Identification of the DNA binding landscape of the transcription factor regulatory factor X 7 (RFX7) in Nutlin-3a and DMSO control treated RPE-1 cells. Overall design: RFX7 ChIP-seq in Nutlin-3a and D
