<HashMap><database>biostudies-arrayexpress</database><scores/><additional><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><submitter>Iris Zhu</submitter><study_type>transcription profiling by array</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-GEOD-44175</full_dataset_link><description>The effect of HMGN1 protein on gene expression of mouse ESC, NP and Neurons were investigated by comparing the transcriptome between Hmgn1+/+ and Hmgn1 -/- cells. three cell types, two genotypes, three reps per sample type</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - Total RNA was isolated by RNeasy Mini Kit (Qiagen) followed by “on-column” DNase I treatment according to the manufacturer's instructions.</sample_protocol><sample_protocol>Growth Protocol - The ES cells were co-cultured with mitomycin-c treated mouse primary embryonic fibroblast feeders or cultured under feeder-free conditions, they were maintained in Knock-out Dulbecco’s modified Eagle’s medium, with 20% serum replacement, 0.055 mM β-mercaptoethanol, 2mM L-glutamine, 0.1mM MEM non-essential amino acid, 5000 U/ml penicillin/streptomycin, and 1000 U/ml LIF. In vitro differentiation of ES cells along neural lineage was performed using the Mouse Dopaminergic Neuron Differentiation Kit (R&amp;D System) according to the manufacturer’s instruction.</sample_protocol><sample_protocol>Hybridization - Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on Mouse Genome 430 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station.</sample_protocol><sample_protocol>Labeling - Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA.</sample_protocol><figure_sub>MIAME Score</figure_sub><figure_sub>Raw Data</figure_sub><figure_sub>Organization</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><pubmed_authors>David Landsman</pubmed_authors><pubmed_authors>Tao Deng</pubmed_authors><pubmed_authors>Iris Zhu</pubmed_authors><pubmed_authors>Michael Bustin</pubmed_authors><data_protocol>Image Adquisition - Scanning was performed with the Affymetrix GeneChip scanner using default settings.</data_protocol><data_protocol>Assay Data Transformation - ID_REF =  VALUE = normalized signal intensity</data_protocol><data_protocol>Feature Extraction - All analysis was performed using R and BioConductor. Expression levels were derived using the Robust Multichip Average (RMA) protocol with default setting and differentially expressed genes were identified using an empirical Bayes method implemented in the R package “Limma”</data_protocol></additional><is_claimable>false</is_claimable><name>Expression data from mouse embyonic stem cell, neural progenitor and neuron</name><description>The effect of HMGN1 protein on gene expression of mouse ESC, NP and Neurons were investigated by comparing the transcriptome between Hmgn1+/+ and Hmgn1 -/- cells. three cell types, two genotypes, three reps per sample type</description><dates><release>2013-02-09T00:00:00Z</release><modification>2023-08-26T17:38:38.739Z</modification><creation>2022-02-07T23:29:29.107Z</creation></dates><accession>E-GEOD-44175</accession><cross_references><GEO>GSE44175</GEO><EFO>EFO_0002768</EFO></cross_references></HashMap>