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Sample GSM497898 Query DataSets for GSM497898
Status Public on Jun 14, 2010
Title UC_0042_1_Hv3_35k_h1
Sample type RNA
 
Channel 1
Source name Urinary bladder tumor UC_0042_1
Organism Homo sapiens
Characteristics sample histology: Urothelial carcinoma
tumor stage: Ta
tumor grade: G2
dead of disease: NO
follow up time (months): 68.8
tat1 progress^to minv/cystectomy/dead: NO
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_0042_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 2.957255835
1175 0.811367476
1750
1751 0.92459989
2901 -0.926358682
2902
2903
2904 0.113856904
3479 -1.622098908
3480 0.933864461
4052 -0.747708402
4054 1.414421726
4055
4056 0.393152446
5206 -1.15100978
5208 -0.591528485
5784 0.905252531
6358
6359 0.163342297
6360

Total number of rows: 20866

Table truncated, full table size 310 Kbytes.




Supplementary file Size Download File type/resource
GSM497898.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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