<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Christophe RACHEZ</submitter><organism>Mus musculus</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15194</full_dataset_link><description>Expression profiling by high throughput sequencing in Bi-potential Murine Embryonic Liver cells (BMEL cells). Three clones (TKO1, TKO2, TKO3) of BMEL TKO cells invalidated for the expression of the three HP1 isoforms (Cbx1-/-; Cbx3-/-; Cbx5-/-), compared to three clones (Het1, Het32, Het35) of BMEL Het cells (Cbx1+/+; Cbx3+/+; Cbx5+/-) expressing HP1 as controls. Expression profiling was performed on total cell extracts, on cytosolic RNA and on chromatin-enriched RNA.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Library sequencing was performed by Novogene Co, Ltd, as Paired End 150 sequencing (30G raw data/sample).</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted out of nucleosol, chromatin, or total cells by guanidinium thiocyanate-phenol-chloroform extraction followed by proteinase K and Dnase I treatment.</sample_protocol><sample_protocol>Library Construction - Total RNA library preparation was performed by Novogene Co., Ltd, as a lncRNA sequencing service, including lncRNA directional library preparation with rRNA depletion (Ribo-Zero Magnetic Kit)</sample_protocol><sample_protocol>Sample Collection - Cytosolic and chromatin-enriched fractions were obtained by sequential lysis and centrifugation steps giving a cytosolic fraction, followed by nuclei lysis and centrifugation giving a nuclear soluble fraction and a chromatin pellet.</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 - Bigwig files were generated from BAM files with bamCoverage (parameter: –normalizeUsing CPM) from Deeptools (v3.1.3).</data_protocol><data_protocol>Sequence Alignment - Mapping was carried out with STAR (v2.6.0b) (parameters: –outFilterMismatchNmax 1 – outSAMmultNmax 1 –outMultimapperOrder Random –outFilterMultimapNmax 30) on Mus musculus mm10 genome.</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>RNA-seq of total RNA</study_type><species>Mus musculus</species><pubmed_authors>Christophe RACHEZ</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNAseq of BMEL cell lines invalidated or not for the expression of the three HP1 isoforms (CBX1, CBX3, CBX5)</name><description>Expression profiling by high throughput sequencing in Bi-potential Murine Embryonic Liver cells (BMEL cells). Three clones (TKO1, TKO2, TKO3) of BMEL TKO cells invalidated for the expression of the three HP1 isoforms (Cbx1-/-; Cbx3-/-; Cbx5-/-), compared to three clones (Het1, Het32, Het35) of BMEL Het cells (Cbx1+/+; Cbx3+/+; Cbx5+/-) expressing HP1 as controls. Expression profiling was performed on total cell extracts, on cytosolic RNA and on chromatin-enriched RNA.</description><dates><release>2026-03-31T00:00:00Z</release><modification>2026-03-31T01:03:47.056Z</modification><creation>2025-06-09T11:09:32.178Z</creation></dates><accession>E-MTAB-15194</accession><cross_references><ENA>ERP173145</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0009653</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>