<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Neus Visa</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-17179</full_dataset_link><description>CUT&amp;Tag was performed to identify the effect of DIS3 depletion on DNA:RNA hybrids genome-wide. DIS3-AID HCT116 cells were treated with either Auxin (for rapid depletion of DIS3) or DMSO (control). CUT&amp;Tag was performed targeting DNA:RNA hybrids using the CUT&amp;Tag-IT® R-loop Assay Kit (Active Motive) with the S9.6 antibody.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - DIS3-AID HCT116 human cell line from Davidson et al. (doi: 10.1016/j.celrep.2019.02.012). DIS3-AID cells were treated with either Auxin (for rapid depletion of DIS3) or DMSO (control). CUT&amp;Tag was performed using CUT&amp;Tag-IT® R-loop Assay Kit (Active Motif, cat. no. 53167) according to manufacturer's instructions.</sample_protocol><sample_protocol>Growth Protocol - Cells were cultured at 37°C in a humidified incubator with 5% CO2, in DMEM supplemented with Penicillin and Streptomycin and 10% of heat-inactivated fetal bovine serum.</sample_protocol><sample_protocol>Nucleic Acid Extraction - The DNA was extracted using SPRI beads provided as kit component.</sample_protocol><sample_protocol>Sequencing - Samples were sequenced on a Nextseq 2000 P3 100 Flowcell.</sample_protocol><sample_protocol>Sample Treatment - DIS3-AID cells were treated with either 500 μM  Auxin or DMSO.</sample_protocol><sample_protocol>Library Construction - Q5 Polymerase master mix was used for library enrichment, using uniquely barcoded i5 and i7 primers.</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 - The CPM normalization was performed using the  nf-core cutandrun pipeline (v3.2.2).</data_protocol><data_protocol>Sequence Alignment - CUT&amp;TAG data was preprocessed using the nf-core cutandrun pipeline (v3.2.2) using the following parameters: nextflow run nf-core/cutandrun \   -r 3.2.2 \   --input samplesheet_18exp.csv \   --genome hg38 \   --spikein_genome dm6 \   --igenomes_base /sw/data/igenomes \   --use_control false \   --peakcaller macs2 \   --macs2_narrow_peak true \   --macs2_qvalue 0.05 \   --blacklist \"${PWD}/hg38-blacklist.v2.bed\" \   --consensus_peak_mode group \   --replicate_threshold 2 \ BAM files were converted to bigWig files using bamCoverage.</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>NextSeq 2000</instrument_platform><study_type>CUT&amp;Tag</study_type><species>Homo sapiens</species><pubmed_authors>Shruti Jain</pubmed_authors><pubmed_authors>Neus Visa</pubmed_authors></additional><is_claimable>false</is_claimable><name>CUT&amp;Tag for S9.6 in DIS3-depleted cells</name><description>CUT&amp;Tag was performed to identify the effect of DIS3 depletion on DNA:RNA hybrids genome-wide. DIS3-AID HCT116 cells were treated with either Auxin (for rapid depletion of DIS3) or DMSO (control). CUT&amp;Tag was performed targeting DNA:RNA hybrids using the CUT&amp;Tag-IT® R-loop Assay Kit (Active Motive) with the S9.6 antibody.</description><dates><release>2026-08-03T00:00:00Z</release><modification>2026-08-03T10:02:49.21Z</modification><creation>2026-06-17T14:47:02.269Z</creation></dates><accession>E-MTAB-17179</accession><cross_references><ENA>ERP195285</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>