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Status |
Public on Mar 07, 2022 |
Title |
PBMC-07-3-GEX-S7 |
Sample type |
SRA |
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Source name |
peripheral blood mononuclear cells
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Organism |
Homo sapiens |
Characteristics |
batchid: PBMC-07 subbatchid: 3 sequencingrunid: S7 librarytype: Gene Expression
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Extracted molecule |
polyA RNA |
Extraction protocol |
A pooled suspension containing 2,000,000 thawed PBMCs from at most 20 subjects (~100,000 per subject) were stained with 282 Totalseq antibodies according to the Totalseq-A protocol (https://www.biolegend.com/en-us/protocols/totalseq-a-antibodies-and-cell-hashing-with-10x-single-cell-3-reagent-kit-v3-3-1-protocol). Stained cells were then loaded onto the Chromium Controller at an input density of 2,500 cells/µL and cDNA libraries were prepared using the 10X Genomics Single Cell 3' v3.1 Assay. Peripheral blood was collected from each subject in Vacutainer ACD tubes. PBMCs were isolated using a standard Ficoll method and stored in liquid nitrogen.
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
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Description |
PBMC-07-3.barcodes.tsv.gz PBMC-07-3.features.tsv.gz PBMC-07-3.matrix.mtx.gz
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Data processing |
Library strategy: CITE-seq Raw RNA and ADT fastqs for each Chromium library were respectively aligned to the GRCh38 human genome reference and a reference database of antibody-tag sequences using Cell Ranger 3.1.0 Genome_build: GRCh38 Supplementary_files_format_and_content: CellMetadata_AS_20220103.tsv, CellMetadata_PSA_20220103.tsv: metadata for each barcode (cell type, subject, subject clinical status, whether the cell was identified to be a doublet, etc.); barcodes.tsv.gz: cell barcodes in the sample; features.tsv.gz: Gene and ADT features detected in a sample; matrix.mtx.gz: MTX (MatrixMarket)-formatted read counts in a sample of each feature in the corresponding features.tsv.gz file in each barcode in the corresponding barcodes.tsv.gz file
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Submission date |
Jan 25, 2022 |
Last update date |
Mar 07, 2022 |
Contact name |
Wilson Liao |
E-mail(s) |
wilson.liao@ucsf.edu
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Organization name |
University of California, San Francisco
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Department |
Dermatology
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Street address |
2340 Sutter St.
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City |
San Francisco |
State/province |
CA |
ZIP/Postal code |
94143 |
Country |
USA |
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Platform ID |
GPL24676 |
Series (1) |
GSE194315 |
RNA and surface epitope sequencing of single cells involved in spondyloarthritis |
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Relations |
BioSample |
SAMN25241897 |
SRA |
SRX13897046 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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