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Sample GSM4732034 Query DataSets for GSM4732034
Status Public on Jul 01, 2024
Title control 2
Sample type SRA
 
Source name peripheral blood
Organism Homo sapiens
Characteristics tissue: peripheral blood
disease state: Health control
treatment: untreated
Extracted molecule total RNA
Extraction protocol PBMCs were isolated from PB using Ficoll Hypaque gradient centrifugation
PCR products were purified and library quality was assessed on the Agilent Bioanalyzer 2100 system. Then, the library preparations were sequenced on an Illumina platform and 125 bp /150 bp paired-end reads were generated.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description single-cell RNA
Data processing Reads mapping, sample merge and single-cell counting was performed using the Cell Ranger Single-Cell Software Suite (10x Genomics).
Cell ranger count was used to align samples to the reference genome (GRCh38, download from 10xgenomics.com).
The Seurat package in R was used for subsequent analysis. For quality control, nuclei with mitochondrial content >15% were removed.
Principal component analysis was performed prior to clustering and the first 20 principal components were used based on the Elbow Plot.
Genome_build: GRCh38
 
Submission date Aug 19, 2020
Last update date Jul 01, 2024
Contact name Dunmin She
E-mail(s) sdm1979@126.com
Phone +862166111061
Organization name Northern Jiangsu People’s Hospital
Department Endocrinology
Street address 98,Western Nantong
City Yangzhou
State/province CHINA
ZIP/Postal code 225000
Country China
 
Platform ID GPL11154
Series (2)
GSE156464 Single cell RNA-sequencing of PBMCs in FOP patients
GSE156466 RNA-Seq of peripheral blood in FOP patients
Relations
BioSample SAMN15856725
SRA SRX8969370

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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