<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Lízia Branco</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-17432</full_dataset_link><description>This dataset contains single-cell RNA sequencing data generated from nine dorsal forebrain organoids collected at day 90 of differentiation. The organoids were derived from three human induced pluripotent stem cell lines: KOLF2.1J, BIONi010-C, and HMGU1. The primary objective of the study was to explore potential neurodevelopmental and differentiation-related differences among these lines, with a specific focus on the KOLF2.1J line, in which previously undetected structural variants were identified through optical genome mapping and long-read sequencing.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Libraries were sequenced on the Illumina NovaSeq 6000 system.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Approximately 25,000 cells per channel were loaded onto a Chromium Single Cell 3′ Chip (10x Genomics, Cat. no. PN-120236) and processed through the Chromium controller to generate single-cell gel beads in emulsion.</sample_protocol><sample_protocol>Library Construction - Library preparation was carried out according to the manufacturer’s protocol. Feature barcode libraries were created using a 10X accessory kit.</sample_protocol><sample_protocol>Sample Collection - Dorsal forebrain organoids were enzymatically dissociated using the Worthington Papain Dissociation System kit (Worthington Biochemical, Cat. no. LK003150). Multiplexing was performed by 3' CellPlex Kit Set A (10x Genomics, Cat. no. PN-1000261) following the manufacturer’s instructions. Multiplexed cells were counted and pooled in equal proportions to be processed by CeGat Tübingen for single cell sequencing.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><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 NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA from single cells</study_type><species>Homo sapiens</species><pubmed_title>Characterization of structural variants in KOLF2.1J iPSCs and their potential impact on forebrain organoid differentiation</pubmed_title><pubmed_authors>Zeynep Yentür</pubmed_authors><pubmed_authors>Lízia Branco</pubmed_authors><pubmed_authors>Lízia Branco, Zeynep Yentür, Madison James Yang, Parithi Balachandran, Kamilla Sedov, G Kumar, Faria Zafar, Theresa Kagermeier, Kseniia Sarieva, Katharina Becker, Bill Skarnes, Christine Beck, Birgitt Schüle, Simone Mayer</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell RNA sequencing data of human dorsal forebrain organoids derived from three iPSC lines</name><description>This dataset contains single-cell RNA sequencing data generated from nine dorsal forebrain organoids collected at day 90 of differentiation. The organoids were derived from three human induced pluripotent stem cell lines: KOLF2.1J, BIONi010-C, and HMGU1. The primary objective of the study was to explore potential neurodevelopmental and differentiation-related differences among these lines, with a specific focus on the KOLF2.1J line, in which previously undetected structural variants were identified through optical genome mapping and long-read sequencing.</description><dates><release>2026-08-03T00:00:00Z</release><modification>2026-08-03T10:57:27.991Z</modification><creation>2026-07-31T11:42:13.428Z</creation></dates><accession>E-MTAB-17432</accession><cross_references><ENA>ERP203142</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005684</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>