<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter/><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14066</full_dataset_link><description>Proof of principle and optimization experiment on cardioid with10X-based-iPS2-seq was performed on two batches of hPSC-derived cardioids at day 7.5 and pooled together after sample multiplexing. hPSC were primed and treated with Tetracycline 5 days prior cardiac differentiation. CG000388 Rev B (when multiplexing) User Guide was followed with sample multiplexing, provided information of the multiplexing for the cellranger aggr is provided. Sequencing has been performed on a Nextseq 1000 on a P2 Illumina kit 100 cycles. Sequencing run: Read1, 28 cycles; Index1, 10 cycles; Index2, 10 cycles, Read2, 90 cycles.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - CG000388 Rev B (with cell multiplexing oligos). hPS-2seq barcode enrichment protocol was performed with custom primers binding on the TET repressor.</sample_protocol><sample_protocol>Nucleic Acid Extraction - 10X genomics technology with CG000388 Rev B (with cell multiplexing oligos). Cells were loaded on a chip G.</sample_protocol><sample_protocol>Sample Collection - Digestion with versene and trippleE. Then cells were labeled with CMO, sorted for vital cells and then loaded on the 10X controller.</sample_protocol><sample_protocol>Sequencing - Nextseq 1000 P2 100 cycles. Cell multiplexing barcodes were pulled in molar ratio compared to the gen expression library 1:6. hPS2seq barcodes were pulled in molar ratio compared to the gen expression library 1:20.</sample_protocol><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>organisation</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - Data provided are row. Use the atached aggregation.csv and config.csv files to run cell ranger aggr (aggregation.csv) and then cell ranger multi (config.csv)</data_protocol><data_protocol>Data Transformation - shRNA information is atached to allow running CatcheR.</data_protocol><data_protocol>Data Transformation - an RDS file is atached with the full processed data. Data can be read with readRDS() function in R and then it can be read and used with monocle 3. Additional txt files with data annotation and count data are  provided to be analyzed with different platforms.</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>NextSeq 1000</instrument_platform><study_type>RNA-seq of coding RNA from single cells</study_type><species>Homo sapiens</species><additional_accession>E-MTAB-14065</additional_accession><pubmed_authors>Elisa Balmas</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proof of principle for iPS2-10X-seq: cardioids experiment during 3D cardiac differentiation</name><description>Proof of principle and optimization experiment on cardioid with10X-based-iPS2-seq was performed on two batches of hPSC-derived cardioids at day 7.5 and pooled together after sample multiplexing. hPSC were primed and treated with Tetracycline 5 days prior cardiac differentiation. CG000388 Rev B (when multiplexing) User Guide was followed with sample multiplexing, provided information of the multiplexing for the cellranger aggr is provided. Sequencing has been performed on a Nextseq 1000 on a P2 Illumina kit 100 cycles. Sequencing run: Read1, 28 cycles; Index1, 10 cycles; Index2, 10 cycles, Read2, 90 cycles.</description><dates><release>2025-10-27T00:00:00Z</release><modification>2025-10-27T09:34:29.117Z</modification><creation>2024-05-10T18:09:09.116Z</creation></dates><accession>E-MTAB-14066</accession><cross_references><ENA>ERP160155</ENA><Biostudies>E-MTAB-14065</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>