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Sample GSM497962 Query DataSets for GSM497962
Status Public on Jun 14, 2010
Title UC_0323_1_Hv3_35k_h1
Sample type RNA
 
Channel 1
Source name Urinary bladder tumor UC_0323_1
Organism Homo sapiens
Characteristics sample histology: Urothelial carcinoma
tumor stage: T2^Nested
tumor grade: G3^Nested
dead of disease: YES
follow up time (months): 1.3
Extracted molecule total RNA
Extraction protocol Tissue homogenization and RNA recovery using TRIzol reagent (Invitrogen), followed by purification of total RNA using RNeasy kit (Qiagen).
Label Cy3
Label protocol Labeling of 5 micrograms of sample RNA was performed using the Pronto Plus System (Promega)
 
Channel 2
Source name Stratagene Universal Human Reference
Organism Homo sapiens
Characteristics reference: RNA pooled from ten human cell lines
Extracted molecule total RNA
Extraction protocol Tissue homogenization and RNA recovery using TRIzol reagent (Invitrogen), followed by purification of total RNA using RNeasy kit (Qiagen).
Label Cy5
Label protocol Labeling of 5 micrograms of sample RNA was performed using the Pronto Plus System (Promega)
 
 
Hybridization protocol Samples were dissolved in 42 microliter Universal Hybridization Solution (Corning) and hybridizations were carried out in a CMT-Hybridization Chamber (Corning) for 18 h at 42°C. Pre-hybridization of slides and post-hybridization washes were performed using the Pronto Plus System (Promega)
Scan protocol Fluorescence was recorded using an Agilent G2565AA microarray scanner (Agilent Technologies). Image analysis on scanned arrays was performed with GenePix 4.0 (Axon Instruments)
Description UC_0323_1_Hv3_35k_h1
Data processing Data was processed in the BioArray Software Environment (BASE). For each channel, the Mean FG - Median BG intensity value was used. Features flagged bad, missing or saturated during image analysis were removed. Poorly measured features with ch1 or ch2 intensities <15 were removed. Data was normalized using pin-based LOWESS algorithm.
 
Submission date Jan 15, 2010
Last update date Jan 19, 2010
Contact name David Lindgren
E-mail(s) david.lindgren@med.lu.se
Organization name Lund University
Department Dept of Laboratory Medicine
Lab Translational Cancer Research
Street address Building 404 A3, Scheelevägen 2, Medicon Village
City Lund
ZIP/Postal code SE-223 81
Country Sweden
 
Platform ID GPL5186
Series (1)
GSE19915 Subtype classification, grading, and outcome prediction of urothelial carcinomas by combined mRNA profiling and aCGH

Data table header descriptions
ID_REF
VALUE normalized log2 ratio (Cy3/Cy5) representing test/reference

Data table
ID_REF VALUE
599 2.53730756
1175 0.623632667
1750
1751 0.349870566
2901 0.421493545
2902
2903
2904 -0.316753211
3479 -1.548834719
3480 0.612831083
4052 -1.055765651
4054 0.025274911
4055
4056
5206 -0.023432657
5208 -0.584920847
5784
6358
6359 0.72262513
6360 2.705949751

Total number of rows: 20866

Table truncated, full table size 290 Kbytes.




Supplementary file Size Download File type/resource
GSM497962.gpr.gz 2.7 Mb (ftp)(http) GPR
Processed data included within Sample table
Processed data are available on Series record

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