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Sample GSM3433443 Query DataSets for GSM3433443
Status Public on Jul 31, 2020
Title CD8-rep1
Sample type SRA
 
Source name T cells
Organism Mus musculus
Characteristics strain: B-NDG
tissue: Spleen
cell type: T cells
cell subtype: CD8
Treatment protocol 1000 T cells were sorted for RNAseq analysis.
Growth protocol The process cells derived from ESC/iPSC.
Extracted molecule polyA RNA
Extraction protocol The procedure of RNA extraction and reverse transcription into double-stranded DNA were prepared using Discover-sc WTA Kit V2(Vazyme, N711)
Libraries were prepared according to instruction of TruePrepTM  DNA Library Prep Kit V2 (Vazyme,TD503).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Data processing Bcl2fastq convert .bcl files into fastq files
Fastq files were aligned to mm10 genome.*.ht2 files to generate *.sam file by HISAT2. And the used samtools to convert and sort the sam file to bam file. StringTie were used to calculated genes expression level in TPM.
Gene expression levels of different samples were normalized by Stringtie, and finally generated TPM table with R
Genome_build: mm10
Supplementary_files_format_and_content: TPM table was a csv file
 
Submission date Oct 17, 2018
Last update date Jul 31, 2020
Contact name Jinyong Wang
E-mail(s) wang_jinyong@gibh.ac.cn
Organization name Guangzhou Institutes of Biomedicine and Health (GIBH)
Street address 190 Kai Yuan Avenue, Science Park, Guangzhou, China
City Guangzhou
State/province GuangDong
ZIP/Postal code 510530
Country China
 
Platform ID GPL19057
Series (2)
GSE121373 T cell regeneration from pluripotent stem cells by defined transcription factors [T cells [CD4 and CD8])
GSE121375 T cell regeneration from pluripotent stem cells by defined transcription factors
Relations
BioSample SAMN10250650
SRA SRX4896778

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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