<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Rajiv Sanwal</submitter><organism>Mus musculus</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15283</full_dataset_link><description>To determine the effect of Aeroplysinin-1 (Ap) on gene expression, we treated murine RAW264.7 macrophages (ATCC TIB-71) with DMSO control or Aeroplysinin-1 (1uM) for 2 hours. Unstimulated and LPS stimulated (0.1ug/mL) conditions were investigated. Three biological replicates were used per group for RNASeq analysis. Derivatives of Aeroplysinin-1 were also tested (Ap7, Ap-9) at the same concentration and time points. Aligned reads</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - Lysates were prepared by washing cells twice with PBS+, lysed in recommended volume of RLT Lysis buffer from the Qiagen RNeasy RNA Isolation Kit (Cat. No. / ID: 74104) and collected by scraping with a sterile cell scraper. Lysates were vortexed for 20 seconds, centrifuged at max speed for 3 minutes at room temperature at stored at -80C for up to two weeks.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA was isolated using Qiagen RNeasy RNA Isolation Kit (Cat. No. / ID: 74104) by following the manufacturer's instructions.</sample_protocol><sample_protocol>Library Construction - Library prep was performed using the NEB Ultra II Directional mRNA kit.</sample_protocol><sample_protocol>Sequencing - Sequencing was performed with the Illumina Hiseq2500 platform with high throughput Flowcell PE2x125bp (paired end 2x125 base pair configuration), with 25-30 million reads per sample.</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 - Two-condition differential gene expression analysis was performed with DESeq2 (https://bioconductor.org/packages/release/bioc/html/DESeq2.html and http://master.bioconductor.org/packages/release/workflows/vignettes/rnaseqGene/inst/doc/rnaseqGene.html) v. 1.26.0s, using R v.3.6.1.  Initial minimal filtering of 10 read counts per gene for at least 3 samples was applied to the dataset. More strict filtering to increase power is automatically applied via independent filtering on the mean of normalized counts within the DESeq results() function. Note: The genes that are filtered out have padj (FDR) value of “NA”.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina HiSeq 2500</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Mus musculus</species><pubmed_authors>Alexandre Hardy</pubmed_authors><pubmed_authors>Rajiv Sanwal</pubmed_authors><pubmed_authors>Elyse Latreille</pubmed_authors><pubmed_authors>Bhooma Thiruvahindrapuram</pubmed_authors><pubmed_authors>Warren Lee</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-Seq: Effect of Aeroplysinin-1 on gene expression in Murine RAW264.7 macrophages in basal and LPS stimulated conditions (2hours)</name><description>To determine the effect of Aeroplysinin-1 (Ap) on gene expression, we treated murine RAW264.7 macrophages (ATCC TIB-71) with DMSO control or Aeroplysinin-1 (1uM) for 2 hours. Unstimulated and LPS stimulated (0.1ug/mL) conditions were investigated. Three biological replicates were used per group for RNASeq analysis. Derivatives of Aeroplysinin-1 were also tested (Ap7, Ap-9) at the same concentration and time points. Aligned reads</description><dates><release>2025-07-14T00:00:00Z</release><modification>2025-06-27T08:17:12.509Z</modification><creation>2025-06-27T08:17:12.509Z</creation></dates><accession>E-MTAB-15283</accession><cross_references><ENA>ERP174132</ENA><Biostudies>E-MTAB-15177</Biostudies><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>