|
Status |
Public on Feb 17, 2010 |
Title |
Renal_Cell_Carcinoma_C11 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
Renal Clear Cell Carcinoma
|
Organism |
Homo sapiens |
Characteristics |
identifier: C11 tissue: kidney histology: Clear Cell disease state: Clear Cell Carcinoma biosourcetype: Frozen Sample
|
Biomaterial provider |
BioSource Provider: University of North Carolina
|
Extracted molecule |
total RNA |
Extraction protocol |
Frozen RCCs were obtained through University of North Carolina - Chapel Hill's Tissue Procurement Facility RNA was extracted with a Qiagen RNeasy kit. RNA quality was determined using an Agilent LabChip Bioanalyzer. H&E was performed on tumor tissue samples to confirm clear cell or normal histopathology
|
Label |
Cy5
|
Label protocol |
Tumor sample RNA and reference RNA was labelled using the Agilent Two-Color Microarray-Based Gene Expression Analysis v 5.2 protocol by UNC Lineberger Comprehensive Cancer Center Genomics Core.
|
|
|
Channel 2 |
Source name |
Perou lab reference RNA
|
Organism |
Homo sapiens |
Characteristics |
biosourcetype: Cancer cell lines cell line: various cancer cell lines (reference)
|
Extracted molecule |
total RNA |
Extraction protocol |
Frozen RCCs were obtained through University of North Carolina - Chapel Hill's Tissue Procurement Facility RNA was extracted with a Qiagen RNeasy kit. RNA quality was determined using an Agilent LabChip Bioanalyzer. H&E was performed on tumor tissue samples to confirm clear cell or normal histopathology
|
Label |
Cy3
|
Label protocol |
Tumor sample RNA and reference RNA was labelled using the Agilent Two-Color Microarray-Based Gene Expression Analysis v 5.2 protocol by UNC Lineberger Comprehensive Cancer Center Genomics Core.
|
|
|
|
Hybridization protocol |
Tumor sample RNA and reference RNA were hybridized on Agilent Whole Human Genome 4x44k arrays by UNC Lineberger Comprehensive Cancer Center Genomics Core
|
Scan protocol |
Agilent gene chips were scanned on an Agilent model C scanner by UNC Lineberger Comprehensive Cancer Center Genomics Core
|
Description |
Gene expression data from Human RCC sample
|
Data processing |
Data was retrieved from the UNC Microarray Database as LOWESS normalized, log2 of processed Red/Green signal (median), filter for 70% good data (Exclude if spot is not found in either channel, spot or spot background is a non-uniform outlier, spot or spot background is a non-uniform outlier for the population, spot is not a positive and significant signal in either channel, or Ch1 and 2 lowess normalized net (median) <10). Missing data was imputed with KNN (k=10) in SAM. Data from three RNA preparation types was merged using Distance Weighted Discriminant. Each array was standard normalized (subtract the mean of the array and divide by the standard deviation).
|
|
|
Submission date |
Jun 05, 2009 |
Last update date |
Oct 21, 2011 |
Contact name |
Kimryn Rathmell |
E-mail(s) |
kimryn.rathmell@vanderbilt.edu
|
Organization name |
Vanderbilt
|
Department |
Medicine
|
Lab |
Rathmell
|
Street address |
2220 Pierce Ave
|
City |
Nashville |
State/province |
TN |
ZIP/Postal code |
37232 |
Country |
USA |
|
|
Platform ID |
GPL6480 |
Series (1) |
GSE16449 |
Molecular Stratification of Clear Cell Renal Cell Carcinoma Reveals Distinct Subtypes and Survival Patterns |
|
Relations |
Reanalyzed by |
GSE33093 |