|
Status |
Public on May 03, 2013 |
Title |
Id2-GFPhigh Repl2 |
Sample type |
RNA |
|
|
Source name |
Purified Id2-GFPhigh DbNP366-specific CD8+ T cells
|
Organism |
Mus musculus |
Characteristics |
strain background: C57BL/6 genotype/variation: Id2gfp/gfp tissue: Spleen cell type: Db-NP366 specific CD8+ T cells levels of gfp: high
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted using a Qiagen RNeasy Mini Kit followed by DNase treatment . Quality control was performed with Agilent Bioanalyser.
|
Label |
Biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
|
|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Description |
SAMPLE 5
|
Data processing |
The data was background corrected, quantile normalised and log2 transformed (with shift = 16) using neqc function from limma package (v.3.14.4) in R /Bioconductor (v.2.15.2).
|
|
|
Submission date |
Feb 07, 2013 |
Last update date |
May 03, 2013 |
Contact name |
Moshe Olshansky |
E-mail(s) |
[email protected]
|
Organization name |
Walter & Eliza Hall Institute of Medical Research
|
Department |
Bioinformatics
|
Lab |
Speed
|
Street address |
1G Royal Pde
|
City |
Parkville |
State/province |
Victoria |
ZIP/Postal code |
3052 |
Country |
Australia |
|
|
Platform ID |
GPL6887 |
Series (1) |
GSE44140 |
Whole genome mRNA analysis of virus-specific CD8+ T cells expressing different levels of Id2-GFP following influenza virus infection |
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