<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Tao Zhou</submitter><organism>Mus musculus</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16423</full_dataset_link><description>RNA-Seq analyses were performed on GC-1 cells transfected with si-NC (control), si-Senp8, or si-Stat1, to study the regulatory networks between Senp8 and Stat1.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Preliminary quantification was conducted using a Qubit 2.0 Fluorometer, followed by accurate determination of the libraries' effective concentration via RT-qPCR. After successful library validation, the different libraries were pooled based on their effective concentrations and the required data volume for downstream Illumina sequencing.</sample_protocol><sample_protocol>Library Construction - These mRNAs were then randomly fragmented using divalent cations in a specified buffer, and library construction was performed following the NEB standard library construction protocol.</sample_protocol><sample_protocol>Nucleic Acid Extraction - The RNA extracted from the cells was initially subjected to quality control. mRNAs with poly(A) tails were enriched using  oligo(dT) magnetic beads.</sample_protocol><sample_protocol>Sample Collection - The cells (mouse GC-1) were maintained in Dulbecco’s Modified Eagle Medium and Nutrient Mixture F-12 (DMEM/F-12; Gibco, USA), supplemented with 10% fetal bovine serum (FBS;ScienCell, USA), and 1% penicillin-streptomycin solution (NCM Biotech, China).</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 DESeq2 package was used to normalize the raw expression counts, filter low expressed genes, and calculate the deferentially expressed genes between different groups at the transcriptome level. The original p - values were further corrected using the Benjamini and Hochberg (BH) method. Differentially expressed genes were defined based on a fold change > 1.5 and a false discovery rate (FDR) &lt; 0.05.</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>Tao Zhou</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bulk RNA-Seq of GC-1 cells transfected with si-NC, si-Senp8, or si-Stat1</name><description>RNA-Seq analyses were performed on GC-1 cells transfected with si-NC (control), si-Senp8, or si-Stat1, to study the regulatory networks between Senp8 and Stat1.</description><dates><release>2025-12-25T00:00:00Z</release><modification>2026-05-30T15:29:14.802Z</modification><creation>2025-12-18T18:53:31.152Z</creation></dates><accession>E-MTAB-16423</accession><cross_references><ENA>ERP186785</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0009653</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>