<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Juan Garcia</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16224</full_dataset_link><description>To assess the regulation of trophoblast fusion by aPKC-ζ isoforms, PRKCZ-targetting siRNA was transfected into trophoblast stem cells CT29 cell lines which were subsequently used to generate placental organoids. A total of three control and 3 knockdown organoids were sequenced.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - CT29 cell lines were grown and treated with either PRKCZ-targetting siRNA or a scrambled control. The cell lines were used to generate placental organoids.</sample_protocol><sample_protocol>Growth Protocol - CT 29 lines were maintained on 5 µg/mL collagen IV coated plates and using human TSC culture medium in a humidified incubator at 37 degrees and 5% CO2. Organoids were generated using a rotatory cell culture system.</sample_protocol><sample_protocol>Library Construction - Bulk seq libraries were constructed using the Illumina Stranded mRNA Prep Kit.</sample_protocol><sample_protocol>Sample Treatment - CT29 knockdowns were achieved utilizing PRKCZ-targetting siRNA that was transfected into the cell line using Opti-MEM I Reduced Serum Medium and Lipofectamine LTX Reagent with PLUS reagent.</sample_protocol><sample_protocol>Sequencing - Partial lane sequencing was performed via Illumina next generation sequencing (NovaSeq X Plus Series PE150) for 100M read pairs per sample</sample_protocol><sample_protocol>Nucleic Acid Extraction - Placental organoids were pelleted and resuspended in trizol before being mechanically dissociated utilizing a tissue lyser. RNA was extracted by utilizing Invitrogen PureLink RNA Mini Kit.</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>Sequence Alignment - Bulk seq libraries were quality processed and trimmed utilizing the FASTQC pipeline. Trimmed sequenced were mapped to GRCh38/hg38 utilizing STAR v2.7.11</data_protocol><data_protocol>Data Transformation - Data was extracted in Ubuntu utilizing FeatureCounts. Data was analyzed utilizing the DESeq2 package in R.</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>Illumina NovaSeq X</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Meghan Riddell</pubmed_authors><pubmed_authors>Sumaiyah Shaha</pubmed_authors><pubmed_authors>Juan Garcia</pubmed_authors><pubmed_authors>Bethan Wilson</pubmed_authors><pubmed_authors>Ivan Domingo</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA seq of placental organoids generated from CT29 cell lines treated with PRKCZ-targetting siRNA versus control</name><description>To assess the regulation of trophoblast fusion by aPKC-ζ isoforms, PRKCZ-targetting siRNA was transfected into trophoblast stem cells CT29 cell lines which were subsequently used to generate placental organoids. A total of three control and 3 knockdown organoids were sequenced.</description><dates><release>2026-06-25T00:00:00Z</release><modification>2026-06-25T16:11:31.65Z</modification><creation>2025-11-20T13:24:02.694Z</creation></dates><accession>E-MTAB-16224</accession><cross_references><ENA>ERP185411</ENA><Biostudies>E-MTAB-16225</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>