<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Shinkichi Ishikawa</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14782</full_dataset_link><description>Human Pulmonary Alveolar Epithelial Cells (HPAEpiCs) purchased from ScienCell Research Laboratories were cultured at the air-liquid interface (ALI) for 28 days with medium containing Y-27632, A-83-01, and CHIR99021. The gene expression profile of HPAEpiCs was investigated on ALI day 28 by Fixed RNA Profiling.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - HPAEpiCs on ALI day 28 were washed with PBS, incubated in 0.25% trypsin-EDTA, detached from the inserts, and separated by pipetting. Trypsinization was stopped by adding Dulbecco’s Modified Eagle’s Medium supplemented with 10% fetal bovine serum. The cell suspension was then centrifuged, washed, and passed through a 40 µm Flowmi cell strainer (Bel-Art Products, Wayne, NJ, USA). The obtained cells were fixed with 4% formaldehyde in PBS, and subsequently treated with the Quenching Buffer and Enhancer contained in a Chromium Next GEM Single Cell Fixed RNA Sample Preparation Kit (10x Genomics).</sample_protocol><sample_protocol>Library Construction - Isolated single cells were loaded onto a 10x Chromium X (10x Genomics), barcoded, and pre-amplified to construct the sequencing library.</sample_protocol><sample_protocol>Sequencing - The library was sequenced on a DNBSEQ-G400 platform (MGI Tech).</sample_protocol><sample_protocol>Nucleic Acid Extraction - Cell barcoding, amplification, and library construction were performed using a Chromium Fixed RNA Profiling Reagent Kit (10x Genomics) in accordance with the manufacturer's protocol.</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 sequenced reads were subjected to demultiplexing, alignment, barcode counting, UMI counting, and filtering using Cell Ranger (version 7.1.0; 10x Genomics). The human genome (GRCh38-2020-A) was used as a reference to align the reads.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>DNBSEQ-G400</instrument_platform><study_type>RNA-seq of coding RNA from single cells</study_type><species>Homo sapiens</species><pubmed_authors>Shinkichi Ishikawa</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fixed RNA Profiling of HPAEpiCs Cultured at the ALI</name><description>Human Pulmonary Alveolar Epithelial Cells (HPAEpiCs) purchased from ScienCell Research Laboratories were cultured at the air-liquid interface (ALI) for 28 days with medium containing Y-27632, A-83-01, and CHIR99021. The gene expression profile of HPAEpiCs was investigated on ALI day 28 by Fixed RNA Profiling.</description><dates><release>2026-01-01T00:00:00Z</release><modification>2026-01-01T02:02:03.17Z</modification><creation>2025-01-27T20:39:24.852Z</creation></dates><accession>E-MTAB-14782</accession><cross_references><ENA>ERP168680</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>