{"database":"biostudies-arrayexpress","file_versions":[],"scores":null,"additional":{"submitter":["Masahito Yoshihara"],"organism":["Homo sapiens"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14019"],"description":["PAX6-EGFP, TP63-tdTomato reporter iPSCs were cultured using the self-formed ectodermal autonomous multi-zone (SEAM) method (Hayashi et al, Nature 2016). Cells were harvested at 2 weeks, 4 weeks, and 8 weeks."],"repository":["biostudies-arrayexpress"],"sample_protocol":["Library Construction - cDNA libraries were prepared as 118 bp paired-end reads using the Chromium Next GEM Single Cell 5' Kit v2 (10x Genomics)","Sample Collection - iPSCs were seeded at a density of 3,000 cells/well in a six-well plate, 1,000 cells/well in a twelve-well plate, and 500 cells/well in a twenty-four-well plate, containing 500 ng/mL iMatrix-511 silk, and cultured for 10 days. The medium was changed every 2–3 days. For SEAM differentiation, the cells were treated with DM (G-MEM; Thermo Fisher Scientific) supplemented with 10% Knockout Serum Replacement (Thermo Fisher Scientific), 1 mM sodium pyruvate (Thermo Fisher Scientific), 1× MEM non-essential amino acids (Thermo Fisher Scientific), 55 µM monothioglycerol (Wako Pure Chemical), penicillin (Meiji Seika Pharma, Tokyo, Japan), and streptomycin (Meiji Seika Pharma) for 0–28 days; then, the cells were treated with ODM [DM:CnT-Prime without EGF and FGF (CELLnTEC, Bern, Switzerland), 1:1] containing 10 µM Y-27632 (Wako Pure Chemical), 10 ng/mL KGF (Wako Pure Chemical) or EGF for 28–56 days; finally, the cells were treated with OEM (Dulbecco’s modified Eagle medium/F12 (Thermo Fisher Scientific)) containing B27-supplement (Thermo Fisher Scientific), 10 µM Y-27632, and 10 ng/mL KGF or EGF for 56–84 days. TP63-positive cells were collected by FACS.","Nucleic Acid Extraction - RNA extraction was performed per in chip inside 10x Chromium controller.","Sequencing - Libraries were sequenced using a NovaSeq system (Illumina, San Diego, CA, USA)."],"figure_sub":["Organization","MINSEQE Score","Assays and Data","Processed Data","MAGE-TAB Files"],"data_protocol":["Data Transformation - The output count data were analyzed with the R package Seurat (v4.3.0) and normalized and scaled using the SCTransform function."],"omics_type":["Metabolomics","Unknown","Transcriptomics","Genomics","Proteomics"],"instrument_platform":["Illumina HiSeq X"],"study_type":["RNA-seq of coding RNA from single cells"],"species":["Homo sapiens"],"pubmed_authors":["Masahito Yoshihara","Rei Kamuro"],"additional_accession":[]},"is_claimable":false,"name":"Single-cell RNA-sequencing analysis of human iPSC-derived ocular cells","description":"PAX6-EGFP, TP63-tdTomato reporter iPSCs were cultured using the self-formed ectodermal autonomous multi-zone (SEAM) method (Hayashi et al, Nature 2016). Cells were harvested at 2 weeks, 4 weeks, and 8 weeks.","dates":{"release":"2025-07-31T00:00:00Z","modification":"2025-08-01T00:01:47.272Z","creation":"2024-04-18T10:03:09.909Z"},"accession":"E-MTAB-14019","cross_references":{"ENA":["ERP159629"],"Biostudies":["E-MTAB-13992"],"EFO":["EFO_0002944","EFO_0004170","EFO_0005684","EFO_0005518","EFO_0003816","EFO_0004184"]}}