<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Luciano Cascione</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15933</full_dataset_link><description>We investigated the transcriptomic profiles of non-stimulated samples from day 14 of differentiation with those from day 0</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - The libraries have been sequenced using HiSeq2000 in the Genomics Facility of the institute of oncology research</sample_protocol><sample_protocol>Sample Collection - sample preparation began with gel digestion of muscle constructs using Trizol (TR118 MRC), followed by phase separation with 1-Bromo-3-chloropropane (B9673).</sample_protocol><sample_protocol>Library Construction - NEBNext UltraExpress RNA Library Prep Kit for Illumina (New England BioLabs Inc.) was employed with the NEBNext Multiplex Oligos for Illumina (New England BioLabs Inc.) and NEBNext® Poly(A) mRNA Magnetic Isolation Module for cDNA synthesis with the addition of barcode sequences.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA extraction from muscle cells was then performed according to ReliaPrep™ RNA Miniprep Systems’ protocol (Promega), which included DNase treatment.</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>Sequence Alignment - Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to hg38 whole genome using STAR with default paramenters. Genes' Expression have been quantified using HT-Seq count using gencode v22 as gtf.</data_protocol><data_protocol>Data Transformation - Read counts have been normalized with TMM algorithm, and converted into log2 counts per million of mapped reads (cpm)</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 HiSeq 2000</instrument_platform><pubmed_abstract>Image 1.</pubmed_abstract><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_title>Biofabrication of a 3D human skeletal muscle microenvironment to study the early steps of fibrosis</pubmed_title><pubmed_authors>Luciano Cascione</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptomics profile of myobundles' maturation level</name><description>We investigated the transcriptomic profiles of non-stimulated samples from day 14 of differentiation with those from day 0</description><dates><release>2025-10-30T00:00:00Z</release><modification>2026-06-16T12:20:49.558Z</modification><creation>2025-10-30T15:19:51.583Z</creation></dates><accession>E-MTAB-15933</accession><cross_references><ENA>ERP183400</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO><doi>10.1016/j.mtbio.2025.102386</doi></cross_references></HashMap>