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Sample GSM2976841 Query DataSets for GSM2976841
Status Public on Feb 02, 2018
Title H44 6h [27_C4EANACXX_TTAGGC_L007]
Sample type SRA
 
Source name RNA from lysed whole blood cells
Organism Homo sapiens
Characteristics tissue: blood
donor: H44
age: 31
gender: Male
ancestry: Aboriginal
disease status: Healthy
treatment: None
time point: 6h
Treatment protocol RNA was extracted with an RNA Protect Cell Mini Kit (Qiagen, Catalog number 74624).
Growth protocol Cell pellets were suspended in RNAprotect Cell Reagent (Qiagen, Catalog number 76526) and frozen at -80 degrees Celsius until RNA extraction.
Extracted molecule total RNA
Extraction protocol RNA was extracted from pDCs using an RNeasy pus micro kit (Qiagen, catalog number 74034).
RNA libraries were prepared for sequencing using standard Illumina protocols.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description 27_C4EANACXX_TTAGGC_L007
H44 6h
PolyA RNA
processed data file: counts-matrix-EnsembIDs-GRCh37.p10.txt
Data processing Image analysis was performed in real time by the HiSeq Control Software (HCS) v2.2.58 and Real Time Analysis (RTA) v1.18.64, running on the instrument computer. RTA performs real-time base calling on the HiSeq instrument computer. Then the Illumina bcl2fastq 1.8.4 pipeline was used to generate the sequence data.
Reads were mapped to Homo sapiens GRCh37.p10 genome, using TopHat (TopHat v2.0.8, bowtie v2.1.0; Trapnell et al.,2009).
Mapped reads were summarized on a gene level using Ensembl ID gene annotation (Ensembl Release 70 based on GRCh37.p10 genome build) and HTSeq (v0.5.3p9; Anders et al., 2014) software.
Summarised read counts in this submission were NOT normalised nor filtered. We recommend using Bioconductor edgeR package functions: i) calcNormFactors (TMM method) to normalise between samples based on library sizes, and ii) rpkm function to normalise between genes within a sample based on gene lengths.
Genome_build: GRCh37.p10
Supplementary_files_format_and_content: *txt: All processed data files are in a tab-delimited file format. They contain raw read counts summarised on a gene level according to Ensembl Release 70 annotation.
 
Submission date Feb 01, 2018
Last update date Nov 19, 2018
Contact name CSL Research
Organization name CSL Limited / bio21 Institute
Street address 30 Flemington Rd
City Parkville
State/province VIC
ZIP/Postal code 3010
Country Australia
 
Platform ID GPL11154
Series (1)
GSE110041 In-vitro stimulation of healthy donor blood with IL-3 cytokine
Relations
BioSample SAMN08455683
SRA SRX3641448

Supplementary file Size Download File type/resource
GSM2976841_X27_C4EANACXX_TTAGGC_L007.txt.gz 204.0 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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