<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Alma Sophia Barisaac</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16857</full_dataset_link><description>To test the effect of LSm4 on RNA splicing and gene expression, we conducted RNA sequencing in U2OS cells treated with control or two LSm4-targeting siRNAs. In addition, we expressed either LSm4-WT or LSm4-del69-92 in U2OS cells treated with LSm4 siRNA #2.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Sequencing was performed using Illumina NextSeq2000, using P3 XLEAP-SBS 300 cycles (Read1-150; Index1-8; Index2-8; Read2-150) (Illumina, cat no. 20100988) sequencing kit.</sample_protocol><sample_protocol>Sample Collection - RNA was collected from 6-well plates using TRIzol reagent (Ambion) according to the manufacturer's protocol.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was isolated using TRIzol reagent (Ambion) according to the manufacturer's instructions. In brief, chloroform was added and after vortexing, sample was centrifuged for 15 minutes at 12,000 x g, 4 degrees. Upper phase was collected, RNA was precipitated in -20 degrees using glyco blue and isopropanol, and the sample was then centrifuged for 15 minutes at 12,000 x g, 4 degrees. Then, samples were washed with ice-cold 70% ethanol and centrifuged for 5 minutes at 7,500 x g, 4 degrees. Pellet was dried and reconstituted in nuclease-free water on ice.</sample_protocol><sample_protocol>Library Construction - RNA sequencing libraries were prepared using NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB, cat no. E7760).</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 - For differential gene expression analysis, raw sequencing reads were aligned to GENCODE GRCh38 genome assembly using the splice-sensitive aligner HISAT2 (PMID: 25751142) and differential gene analysis was performed in R using the DESeq2 package (PMID: 25516281). Pathway enrichment analysis and gene ontology was conducted using ShinyGO (PMID: 31882993). To analyze alternative splicing events, HISAT2-aligned reads were subjected to alternative splicing events detection using rMATS package (PMID: 25480548).</data_protocol><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>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Alma Sophia Barisaac</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq of U2OS cells treated with control or LSm4-targeting siRNAs, alone or with expression of either LSm4-WT or LSm4-del69-92</name><description>To test the effect of LSm4 on RNA splicing and gene expression, we conducted RNA sequencing in U2OS cells treated with control or two LSm4-targeting siRNAs. In addition, we expressed either LSm4-WT or LSm4-del69-92 in U2OS cells treated with LSm4 siRNA #2.</description><dates><release>2026-04-15T00:00:00Z</release><modification>2026-04-17T01:01:35.282Z</modification><creation>2026-04-02T12:47:15.914Z</creation></dates><accession>E-MTAB-16857</accession><cross_references><ENA>ERP191730</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>