<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Eva Wirth</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14973</full_dataset_link><description>Thyroid hormones are important for many developmental processes. We evaluated the improvement of iPSC-derived hepatocyte-like cell maturation under hypoxic culture conditions, specialized cell culture media, and ±5 nM T3 during the final week of culture in two iPSC lines.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - RNA from samples was extracted with Aurum™ Total RNA Mini Kit (Bio-Rad) according to manufacturer's instructions.</sample_protocol><sample_protocol>Library Construction - Bulk RNA-seq libraries were generated using Poly(A) mRNA selection and prepared with the NEBNext Ultra II RNA Library Prep Kit for Illumina, following the manufacturer’s instructions.</sample_protocol><sample_protocol>Sample Collection - On day 28 of differentiation, the cell culture medium was discarded, and cells were transferred and stored at -80 °C. On the day of RNA extraction, plates were thawed on ice, lysis buffer was added to the culture wells, and the surface was scraped to maximize lysate yield.</sample_protocol><sample_protocol>Sequencing - Sequencing was performed using a paired-end configuration of 2x150 bp, generating approximately 25 million paired-end reads per sample on the Illumina platform.</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 - Processing and analysis of RNA-seq data were performed using an established pipeline from BIH Core Unit Bioinformatics (1). Reads were mapped to GRCh38 (patch release 7) using the STAR aligner (v.2.7.10b; (2)) and counted using the featureCounts command (subreads v2.0.1; (3)) with GENCODE annotation (v25).  1. Pett P. SeA-SnaP: (Se)q (A)nalysis (Sna)kemake (P)ipeline. github.com/bihealth/seasnap-pipeline.  Accessed April 26, 2024. 2. Dobin A, Davis CA, Schlesinger F, Drenkow J, Zaleski C, Jha S, et al. STAR: ultrafast universal RNA-seq aligner. Bioinformatics. 2013;29(1):15-21. 3. Liao Y, Smyth GK, and Shi W. The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote. Nucleic Acids Res. 2013;41(10):e108.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina HiSeq 3000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Eva Wirth</pubmed_authors></additional><is_claimable>false</is_claimable><name>Maturation of iPSC-derived Hepatocyte-Like Cells with 5 nM T3</name><description>Thyroid hormones are important for many developmental processes. We evaluated the improvement of iPSC-derived hepatocyte-like cell maturation under hypoxic culture conditions, specialized cell culture media, and ±5 nM T3 during the final week of culture in two iPSC lines.</description><dates><release>2025-07-31T00:00:00Z</release><modification>2025-03-26T10:08:57.446Z</modification><creation>2025-03-26T10:08:57.446Z</creation></dates><accession>E-MTAB-14973</accession><cross_references><ENA>ERP170844</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>