Comprehensive identification and characterization of the binding sites of Pol2 in mammalian genes were attempted. We used ChIP-Seq method, in which next gene sequencing technology and chromatin-immuno
R-loops are dynamic, co-transcriptional nucleic acid structures that facilitate physiological processes and cause DNA damage in certain contexts. Perturbations of transcription or R-loop resolution ar
ChIP-Seq on HepG2 For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODE_Data_Use_Policy_for_External_Users_03-07-1