<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Lisa DUGAST</submitter><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15460</full_dataset_link><description>CD8 T cells from blood from four healthy volunteers was analysed for several markers by CITEseq and single cell RNAseq.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Single cell libraries were performed according to Chromium Next GEM Single Cell 5' Reagent Kits v2 protocol (10X genomics, San Francisco, CA).</sample_protocol><sample_protocol>Nucleic Acid Extraction - Disintegration of cells or tissues (cell lysis), inactivation of intracellular nucleases, and separation of nucleic acids from the other cell components</sample_protocol><sample_protocol>Sequencing - Cell suspension were loaded onto chromium single cell chip K in 4 different well (20 000 cells per well) and run immediately on the Chromium controller (10X genomics, San Francisco, CA). Three libraries were prepared: one for mRNA (RNA), one for barcoded antibodies (HTO and CITE-seq) and one for TCR (VDJ-seq). They were sequenced with NovaSeq 6000 (Illumina, San Diego, CA) according to 10X genomics recommendations.</sample_protocol><sample_protocol>Sample Collection - Freshly sorted CD8+ T lymphocytes of four healthy volunteers were labelled with anti-human Hashtag antibodies TotalSeq-C (Biolegend, San Diego, CA) and were pooled together.</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 - FASTQ files, first generated from BaseCalling (BCL) files with CellRanger package (6.1.2), were demultiplexed and aligned to human reference genome (hg38). CITE-seq-Count function (1.3.4) was used to count antibody hashtag sequences. Count matrixes were analyzed with Seurat R package (4.1.1). Cells with more than 10% of mitochondrial genes were excluded. Gene expression was log normalized and scaled. HTO expression was normalized and demultiplexed. Doublet cells and negative cells for HTO were removed.</data_protocol><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_authors>Lisa DUGAST</pubmed_authors><pubmed_authors>Carole GUILLONNEAU</pubmed_authors></additional><is_claimable>false</is_claimable><name>CD8 T cells single cell transcriptomic analysis from human blood</name><description>CD8 T cells from blood from four healthy volunteers was analysed for several markers by CITEseq and single cell RNAseq.</description><dates><release>2025-09-01T00:00:00Z</release><modification>2025-09-01T08:19:16.083Z</modification><creation>2025-08-15T10:50:36.531Z</creation></dates><accession>E-MTAB-15460</accession><cross_references><ENA>ERP178813</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>