<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Phaewa Chaiwijit</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15054</full_dataset_link><description>We characterized the different cell types and their differential gene expression at days 10 and 13 of maturation in 2D cortical brain models.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - The iPSC-derived brain cells were trypsinized and dissociated using 0.5% trypsin in PBS, and then resuspended in 0.04% BSA in PBS. A 40-μm strainer was used to remove cell debris and clumps, to obtain single-cell suspension.</sample_protocol><sample_protocol>Library Construction - Single-cell transcriptomic libraries were generated following the Chromium Single-cell 5' Reagent Kits V2 User Guide.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Nucleic acids were extracted following the 10x Genomics Chromium Single Cell 5' Reagent Kits v2 User Guide, up to the cDNA synthesis step. After GEM (Gel Bead-in-Emulsion) generation and reverse transcription, emulsions were broken, and barcoded cDNA was purified using silane magnetic beads, according to the manufacturer’s instructions, with a target recovery of 10,000 cells per sample.</sample_protocol><sample_protocol>Sequencing - Sequencing libraries were generated from 10x Genomics 5' cDNA and sequenced on an Illumina HiSeq X Ten platform. The library from 10-day-old human iPSC-derived brain cells was sequenced across one-third of three lanes, while the library from 13-day-old human iPSC-derived brain cells was sequenced across one-third of a single lane.</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 - Read alignment was performed using Cell Ranger (v6.1.2) against the human reference genome GRCh38. The pipeline generated filtered output matrices, including the gene-barcode matrix (matrix.tsv.gz), corresponding cell barcodes (barcodes.tsv.gz), and gene features (features.tsv.gz).</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 X</instrument_platform><study_type>RNA-seq of coding RNA from single cells</study_type><species>Homo sapiens</species><pubmed_authors>Varodom Charoensawan</pubmed_authors><pubmed_authors>Nithi Asavapanumas</pubmed_authors><pubmed_authors>Phaewa Chaiwijit</pubmed_authors><pubmed_authors>Arunee Thitithanyanont</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identifying GFAP-Expressing Cell Susceptibility to SARS-CoV-2 Infection using Human iPSC-derived neural cells</name><description>We characterized the different cell types and their differential gene expression at days 10 and 13 of maturation in 2D cortical brain models.</description><dates><release>2026-02-17T00:00:00Z</release><modification>2026-02-17T08:32:41.716Z</modification><creation>2025-04-17T10:57:46.431Z</creation></dates><accession>E-MTAB-15054</accession><cross_references><ENA>ERP171770</ENA><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>