<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Sagar Sengupta</submitter><organism>Homo sapiens</organism><software>BWA</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14629</full_dataset_link><description>DREAM complex is known to regulate DNA repair and cell cycle-regulated genes in a p53-p21 dependent axis. This experiment identified an alternate pathway of DREAM target regulation.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - Cells were lysed using a nuclear lysis buffer. Followed by sonication of genomic DNA. 1ng of DNA used for library preparation.</sample_protocol><sample_protocol>Sequencing - Next-generation sequencing oflibraries was performed using the NovaSeq 6000 S4 Reagent Kit v1.5 for the paired-end, 30 million reads.</sample_protocol><sample_protocol>Sample Collection - Cells were harvested from 6 well-plate, followed by trypsinization, crosslinking and fixaton.</sample_protocol><sample_protocol>Library Construction - The Re-ChIP DNA libraries were constructed using the Kapa Hyperprep Kit with sample purification beads according to the manufacturer’s instructions.</sample_protocol><sample_protocol>Sample Treatment - HCT116 p21-/- cell were grown in 6 well plate, without any treatment.  HCT116 p53-/- p53 TAD mutant grown in 6 well in presence of Doxycycline.</sample_protocol><sample_protocol>Growth Protocol - Cells were grown under asynchronous condition in McCoy media</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - Peaks were detected using MACS2 and annotated with ChIPseeker R package.</data_protocol><data_protocol>Sequence Alignment - Bases with a high Phred score (more than 30) were aligned to the current human genome (hg38 assembly) using BWA</data_protocol><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>ChIP-seq</study_type><species>Homo sapiens</species><pubmed_authors>Sagar Sengupta</pubmed_authors></additional><is_claimable>false</is_claimable><name>E2F4-p53 Re-ChIP seq in HCT116 p21-/- cells &amp; HCT116 p53-/- TAD mutant cells</name><description>DREAM complex is known to regulate DNA repair and cell cycle-regulated genes in a p53-p21 dependent axis. This experiment identified an alternate pathway of DREAM target regulation.</description><dates><release>2025-08-23T00:00:00Z</release><modification>2024-11-22T14:48:55.17Z</modification><creation>2024-11-22T14:42:24.766Z</creation></dates><accession>E-MTAB-14629</accession><cross_references><ENA>ERP166451</ENA><Biostudies>E-MTAB-13359</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0002692</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>