<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Lluis Hernandez</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16259</full_dataset_link><description>To characterize the transcriptional impact of MALAT1 in MCL a RNAseq was performed on three SOX11-positive PDLS-MCL samples comparing MALAT1-silenced PDLS to paired controls, all cultured with pro-proliferative factors.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Growth Protocol - Cells were grown with IL4, CD40L, HA-tag and BAFF as described in Araujo et al 2023 (PMID: 37031299)</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted using the RNeasy Plus Micro Kit (Qiagen), quantified with Qubit, and quality-checked using Tapestation 4200 (Agilent).</sample_protocol><sample_protocol>Sample Treatment - Silencing was performed using MALAT1 specific LNA-Gapmer (Qiagen) at 1micromolar vs Scrambled LNA-Gapmer (Qiagen) by gymnotic delivery along 5 days.</sample_protocol><sample_protocol>Sample Collection - Peripheral blood was extracted and PBMC purified with Ficoll and cryopreserved in liquid nitrogen until the day of the experiment.</sample_protocol><sample_protocol>Library Construction - Libraries were prepared from 10 ng of total RNA using the TAKARA_SMART-Seq® Total RNA Pico Input (ZapR® Mammalian) kit (following the manufacturer’s instructions).</sample_protocol><sample_protocol>Sequencing - Libraries were sequenced using a NextSeq2000 (Illumina, Inc.) in paired-end mode with a read length of 2×50 bp, generating more than 60 million paired-end 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 - For the analysis of RNAseq data, ribosomic RNA reads were filtered out using SortMeRNA (version 4.3.4).</data_protocol><data_protocol>Sequence Alignment - Kallisto (version 0.46.1). was used for   high throughput sequence alignment protocol</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>NextSeq 2000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Lluis Hernandez</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNAseq of MALAT1 silencing experiments in three Patient derived lymphoma spheroids (PDLS) from Mantle Cell Lymphoma (MCL) patients</name><description>To characterize the transcriptional impact of MALAT1 in MCL a RNAseq was performed on three SOX11-positive PDLS-MCL samples comparing MALAT1-silenced PDLS to paired controls, all cultured with pro-proliferative factors.</description><dates><release>2026-01-07T00:00:00Z</release><modification>2026-01-07T02:02:39.152Z</modification><creation>2025-11-22T20:43:43.467Z</creation></dates><accession>E-MTAB-16259</accession><cross_references><ENA>ERP185506</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>