<HashMap><database>biostudies-arrayexpress</database><scores/><additional><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><submitter>Mingxia Li</submitter><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-10588</full_dataset_link><description>In order to find out which genes Bap1 regulates to affect the anti-tumor immune response in MC38 colon carcinoma cell linewe knocked out the Bap1 gene in the MC38 cell line through CRISPR-Cas9 technology, RNA was directly isolated for RNA seq and were able to investigate gene expression.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - RNA was breaken into smart fragments with fragment buffer, and cDNAs were synthesized using the RNA fragments as templates, after which NEBNext Adaptor with hairpin loop structure were ligated ,and 3 µl USER Enzyme (NEB, USA) was used with purified adaptor-ligated cDNA at 37°C for 15 m in followed by 5 min at 95 °C before PCR. Then PCR was performed with Phusion High -Fidelity DNA polymerase, Universal PCR primers and Index (X) Primer.</sample_protocol><sample_protocol>Sample Collection - Cell viability was detected with 0.4% trypan blue staining solution and counted with Countess II (Invitrogen) cell counter, and the cell viability was over 90%.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA was extracted with TRIzol reagent (Ambion 15596-026)follow the instructions</sample_protocol><sample_protocol>Sequencing - Sequencing libraries were generated using NEBNext UltraTM RNA Library Prep Kit for Illumina (NEB, USA) following manufacturer’s recommendations, the library preparations were sequenced on an Illumina Novaseq platform.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Mingxia Li</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bulk RNA-Seq analysis of  MC38 colon carcinoma cells and MC38 Bap1-knockout cells in vitro</name><description>In order to find out which genes Bap1 regulates to affect the anti-tumor immune response in MC38 colon carcinoma cell linewe knocked out the Bap1 gene in the MC38 cell line through CRISPR-Cas9 technology, RNA was directly isolated for RNA seq and were able to investigate gene expression.</description><dates><release>2025-07-06T00:00:00Z</release><modification>2023-07-10T16:19:09.363Z</modification><creation>2023-07-10T16:19:09.363Z</creation></dates><accession>E-MTAB-10588</accession><cross_references><ENA>ERP149374</ENA><Biostudies>E-MTAB-10610</Biostudies><Biostudies>E-MTAB-10587</Biostudies><Biostudies>E-MTAB-10593</Biostudies><Biostudies>E-MTAB-10585</Biostudies><Biostudies>E-MTAB-10584</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>