<HashMap><database>biostudies-arrayexpress</database><scores/><additional><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><submitter>Claudia Pommerenke</submitter><study_type>genotyping by array</study_type><organism>Homo sapiens</organism><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15176</full_dataset_link><description>This dataset accompanies our step-by-step guide for analyzing chromosomal integrity in human pluripotent stem cells (hPSCs) using SNP arrays. It includes raw .idat files, a preconfigured GenomeStudio project, the sample sheet, manifest file, and cluster file. The data allows researchers - especially those new to GenomeStudio - to practice data import, normalization, and CNV detection using the cnvPartition plugin. This resource is intended for training and educational use in stem cell quality control workflows.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Nucleic Acid Extraction - Genomic DNA was extracted using the QIAamp DNA Blood Mini Kit (Qiagen).</sample_protocol><sample_protocol>Labeling - Biotin (C and G) or 2,4-Dinitrophenol (DNP) for A and T labelled, the detection is based on fluorophore-labelled antibody (for A/T) and fluorophore-labelled streptavidin (C/G), respectively.</sample_protocol><sample_protocol>Scaning - Samples were processed on Global Screening Array v3.0 (GSAMD24v3-0, Illumina, Inc. San Diego) by LIFE&amp;BRAIN GmbH (Bonn, Germany).</sample_protocol><sample_protocol>Sample Collection - Samples were collectect from cell culture.</sample_protocol><sample_protocol>Hybridization - Samples were processed on Global Screening Array v3.0 (GSAMD24v3-0, Illumina, Inc. San Diego) by LIFE&amp;BRAIN GmbH (Bonn, Germany).</sample_protocol><figure_sub>MIAME Score</figure_sub><figure_sub>Raw Data</figure_sub><figure_sub>Organization</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><pubmed_authors>Claudia Pommerenke</pubmed_authors><data_protocol>Data Transformation - SNP calling was performed using GenomeStudio V2.0.5 with a GenCall threshold of 0.2. CNV Analysis was performed using cnvPartition 3.2.0.</data_protocol></additional><is_claimable>false</is_claimable><name>Chromosomal quality control via SNP array in different hPSC lines</name><description>This dataset accompanies our step-by-step guide for analyzing chromosomal integrity in human pluripotent stem cells (hPSCs) using SNP arrays. It includes raw .idat files, a preconfigured GenomeStudio project, the sample sheet, manifest file, and cluster file. The data allows researchers - especially those new to GenomeStudio - to practice data import, normalization, and CNV detection using the cnvPartition plugin. This resource is intended for training and educational use in stem cell quality control workflows.</description><dates><release>2025-06-03T00:00:00Z</release><modification>2025-06-11T12:12:16.659Z</modification><creation>2025-05-29T09:28:29.197Z</creation></dates><accession>E-MTAB-15176</accession><cross_references><EFO>EFO_0002944</EFO><EFO>EFO_0003814</EFO><EFO>EFO_0003813</EFO><EFO>EFO_0002767</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003815</EFO></cross_references></HashMap>