|
Status |
Public on Jun 07, 2012 |
Title |
T47D_PR_null_yesR5020_6h_rep2 |
Sample type |
RNA |
|
|
Source name |
T47D-Y empty vector cells treated with R5020 for 6 h
|
Organism |
Homo sapiens |
Characteristics |
tissue: breast genotype: PR null parental cell line: T47D-Y ligand treatment: R5020
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with Trizol reagent, followed by clean-up and DNase I treatment with QIAGEN RNeasy mini kit in accordance with the prescribed protocol provided with the kit. 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 |
replicate 2
|
Data processing |
The data were log2 transformed and quantile normalized with Bioconductor lumi package in R.
|
|
|
Submission date |
Dec 05, 2011 |
Last update date |
Feb 01, 2017 |
Contact name |
Todd P Knutson |
E-mail(s) |
[email protected]
|
Phone |
612-626-8911
|
Organization name |
University of Minnesota
|
Department |
Minnesota Supercomputing Institute
|
Street address |
117 Pleasant St SE
|
City |
Minneapolis |
State/province |
MN |
ZIP/Postal code |
55455 |
Country |
USA |
|
|
Platform ID |
GPL10558 |
Series (2) |
GSE34148 |
Phosphorylated and Sumoylation-Deficient Progesterone Receptors Drive Proliferative Gene Signatures During Breast Cancer Progression (Illumina gene expression analysis) |
GSE34149 |
Phosphorylated and Sumoylation-Deficient Progesterone Receptors Drive Proliferative Gene Signatures During Breast Cancer Progression |
|
Relations |
Reanalyzed by |
GSM2474036 |