<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Masahito Yoshihara</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14019</full_dataset_link><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.</description><repository>biostudies-arrayexpress</repository><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_protocol><sample_protocol>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.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA extraction was performed per in chip inside 10x Chromium controller.</sample_protocol><sample_protocol>Sequencing - Libraries were sequenced using a NovaSeq system (Illumina, San Diego, CA, USA).</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 - The output count data were analyzed with the R package Seurat (v4.3.0) and normalized and scaled using the SCTransform function.</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 X</instrument_platform><study_type>RNA-seq of coding RNA from single cells</study_type><species>Homo sapiens</species><pubmed_authors>Masahito Yoshihara</pubmed_authors><pubmed_authors>Rei Kamuro</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell RNA-sequencing analysis of human iPSC-derived ocular cells</name><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.</description><dates><release>2025-07-31T00:00:00Z</release><modification>2025-08-01T00:01:47.272Z</modification><creation>2024-04-18T10:03:09.909Z</creation></dates><accession>E-MTAB-14019</accession><cross_references><ENA>ERP159629</ENA><Biostudies>E-MTAB-13992</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005684</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>