<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Martin Simon</submitter><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16825</full_dataset_link><description>This study investigates the correlation of lncRNA Neat1 to liver inflammation and fibrosis. Different diets were applied to wt and Neat1 Knockout Mice:  1. normal diet 2. MCS: methionine-choline-supplemented diet 3. MCD: methionine-choline-deficiend diet The samples represent RNA Seq from liver.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - To isolate total RNA from the mouse liver tissues, 200 µl of TRI Reagent® (Zymo Research Europe GmbH, Freiburg, Germany, catalogue no.: R2053) was dispensed into a 1.5 ml reaction tube. The liver tissues stored at -80°C were then placed on dry ice for the following procedure. A piece weighing approximately 5 mg was cut off with a scalpel and added to the TRI Reagent®. This was homogenised using the Mixy Professional tissue homogeniser (FastGene® Nippon Genetics, Düren, Germany), a further 200 µl of TRI Reagent® was added, the mixture was vortexed for 10 seconds and centrifuged for 1 minute at room temperature at 14.0 x g. The supernatant was transferred to a fresh 1.5 ml reaction tube and the RNA was then isolated using the kit in accordance with the manufacturer’s instructions. The elution volume was 50 µl.</sample_protocol><sample_protocol>Sequencing - Libraries were dual indexed and sequenced on a Illumina Next Seq 6000S4 lane</sample_protocol><sample_protocol>Sample Collection - Following the three-week feeding period, the mice were euthanised by CO₂ followed by cardiac incision for serum preparation. The livers were excised, weighed and washed in PBS. The liver lobes were divided and each was flash-frozen in liquid nitrogen in a 1.5 ml reaction tube and stored at -80°C.</sample_protocol><sample_protocol>Library Construction - Ribisomal RNA was depeleted using the NEB rRNA depeltion Kit and libraries for Illumina were preared using teh NEB NExt Ultra Express RNA Library Kit with 100ng input RNA</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Martin Simon</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNASeq of mice livers with different genotypes</name><description>This study investigates the correlation of lncRNA Neat1 to liver inflammation and fibrosis. Different diets were applied to wt and Neat1 Knockout Mice:  1. normal diet 2. MCS: methionine-choline-supplemented diet 3. MCD: methionine-choline-deficiend diet The samples represent RNA Seq from liver.</description><dates><release>2026-04-07T00:00:00Z</release><modification>2026-04-07T17:03:06.634Z</modification><creation>2026-03-30T13:11:05.812Z</creation></dates><accession>E-MTAB-16825</accession><cross_references><ENA>ERP191552</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>