<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Patrick Nylund</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-13813</full_dataset_link><description>Here we investigated the molecular response DNMT- and G9a inhibition in multiple myeloma.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Sequencing libraries were prepared from 100ng total RNA using the Illumina Stranded Total RNA library preparation kit with Ribo-Zero Plus treatment (cat# 20040525/20040529, Illumina Inc.)</sample_protocol><sample_protocol>Sample Collection - INA-6, OPM2 and KMS-28PE were selected for combinatorial treatment response analysis. INA-6 and KMS28-PE cells were seeded at 100.000 cells/ml while OPM2 cells were seeded at 200.000 cells/mL 24h prior treatment with H2O and DMSO (Sigma-Aldrich) or 50nM of AZA (Abcam) and 5μM or 10μM of A366 (Tocris Bio-techne). AZA treatment was administrated every day while A366 treatment was added every 3 days. Media and reagent refreshment was performed every 3 days. All experiments were performed in three independent cell batches per cell line.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA was extracted using the RNeasy Micro Kit (Qiagen; Hilden; Germany #74004) as described by the manufacturer.</sample_protocol><sample_protocol>Sequencing - Paired-end 150bp read length, NovaSeq 6000 system, S4 flowcell and v1.5 sequencing chemistry.</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 sequencing data from the combinatorial treated INA-6, KMS-28PE and OPM2 MM cell lines were analysed using the nf-core RNAseq pipeline (https://doi.org/10.5281/zenodo.3503887) in version 3.4, utilizing default parameters for paired-end analysis. Differential expression analysis was done by DESeq2 workflow as described: http://master.bioconductor.org/packages/release/workflows/vignettes/rnaseqGene/inst/doc/rnaseqGene.html</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>Homo sapiens</species><pubmed_authors>Patrick Nylund</pubmed_authors><pubmed_authors>Berta Garrido-Zabala</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq experiment of multiple myeloma cells under different treatment conditions against epigenetic modifiers</name><description>Here we investigated the molecular response DNMT- and G9a inhibition in multiple myeloma.</description><dates><release>2025-12-31T00:00:00Z</release><modification>2025-12-31T02:02:13.02Z</modification><creation>2024-02-28T21:19:02.117Z</creation></dates><accession>E-MTAB-13813</accession><cross_references><ENA>ERP157492</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>