<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Misbah Abbas</submitter><organism>Mus musculus</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-13572</full_dataset_link><description>Hi-C experiment was performed to map and compare potential changes in wildtype and Ddx5 Knockout neural stem cells.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Sequencing was performed using Illumina NovaSeq X-Plus series paired-end, 150bp mode</sample_protocol><sample_protocol>Nucleic Acid Extraction - Hi-C experiments were performed as described as describer before (Rao et al., 2014)</sample_protocol><sample_protocol>Growth Protocol - NS cells were grown on laminin-coated plates in neural differentiation medium containing N2 and B27 supplements along with recombinant murine EGF and bFGF to a final concentration of 10 ng/ml. Cells were split at 80% confluence with a density of 35000 cells/sq.cm. The medium was exchanged daily.</sample_protocol><sample_protocol>Sample Treatment - Ddx5 depletion was carried out in Ddx5-FKBP NS Cells by treating with 500nM of dTAG13 dissolved in culture media for 24h</sample_protocol><sample_protocol>Library Construction - Hi-C libraries were generated using NEBNext Ultra II DNA Library Kit, according to manufacturer's instructions</sample_protocol><sample_protocol>Sequencing - Sequencing was performed using Illumina 6000 platform in paired-end, 100bp mode</sample_protocol><sample_protocol>Sample Collection - Cells were detached with Accutase, counted and crosslinked with 1% (final) formaldehyde in their medium. The reaction was quenched with 0.125M (final) glycine, and cell pellets were washed with PBS, snap-frozen, and stored in a -80 freezer. The pellet of 5 million cells was used for each Hi-C experiment.</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>Sequence Alignment - Reads were aligned to reference genome (mm10) using the juicer pipeline with default settings.</data_protocol><data_protocol>Data Transformation - Normalisation of the data was done automatically as a part of the juicer pipeline</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><instrument_platform>Illumina NovaSeq X</instrument_platform><study_type>Hi-C</study_type><species>Mus musculus</species><pubmed_authors>Bondita Dehingia</pubmed_authors><pubmed_authors>Małgorzata Milewska</pubmed_authors><pubmed_authors>Aleksandra Pękowska</pubmed_authors><pubmed_authors>Debadeep Chaudhury</pubmed_authors><pubmed_authors>Misbah Abbas</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hi-C from mouse embryonic stem cell derived neural stem cells</name><description>Hi-C experiment was performed to map and compare potential changes in wildtype and Ddx5 Knockout neural stem cells.</description><dates><release>2025-07-30T00:00:00Z</release><modification>2025-08-08T11:22:08.106Z</modification><creation>2023-11-27T14:27:36.282Z</creation></dates><accession>E-MTAB-13572</accession><cross_references><ENA>ERP172942</ENA><EFO>EFO_0007693</EFO><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>