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Sample GSM452198 Query DataSets for GSM452198
Status Public on Apr 10, 2011
Title C94
Sample type RNA
 
Source name colon
Organism Homo sapiens
Characteristics localization: distal
gender: male
relapse: no
microsatellite status: MSS
age at diagnosis, years: 62
grading: G1
pt: 3
Extracted molecule total RNA
Extraction protocol For microarray analyses, snap frozen tissue specimens were cut into 7 µm-thick sections that were stained with haematoxylin & eosin (H&E). Stained sections were reviewed by a pathologist to identify areas of vital tumor cells and to ensure a tumor content of 80-90%. Corresponding tumor areas were macrodissected by vertical 3 mm incision into the frozen tissue specimens with a sterile blade. Incision was followed by a series of ten 20 μm frozen sections. Separated tumor areas were harvested by sterile micropipette tip and collected in a buffer (RLT buffer, RNeasy Mini Kit; Qiagen, Hilden, Germany). Each series of ten sections was followed by a 7 µm H&E stained section to control tissue composition. The number of tissue sections used to extract RNA was dependent on the expanse of the area of individual tumor tissue. Total RNA was isolated using the RNeasy Mini Kit (Qiagen) according to the manufacturer’s instructions and quantified using the Nanodrop ND-1000 UV-vis spectrophotometer (Nanodrop Technologies, USA). The quality of the RNA was controlled using the BioAnalyzer (Agilent Technologies, USA) and exclusively high quality RNA was used for further analysis.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 3ug total RNA
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on HG-U133 Plus 2.0 arrays (Affymetrix). GeneChips were washed and stained with standard protocols in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Scanner G3000
Description none
Data processing Data were normalized with VSN (Bioconductor package vsn 3.2.1) and summarized with the median polish method. Data analysis and statistical computing were performed with R (2.6.0).
 
Submission date Sep 11, 2009
Last update date Aug 28, 2018
Contact name Dido Lenze
E-mail(s) [email protected]
Organization name Charité-Universitätsmedizin Berlin
Department Pathologie, Campus Benjamin Franklin
Street address Hindenburgdamm 30
City Berlin
ZIP/Postal code 12200
Country Germany
 
Platform ID GPL570
Series (1)
GSE18088 Correlation of molecular profiles and clinical outcome of stage UICC II colon cancer patients
Relations
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE normalized log2 signal intensity

Data table
ID_REF VALUE
1007_s_at 8.275684749
1053_at 6.981553379
117_at 5.387287513
121_at 6.582351702
1255_g_at 3.90227908
1294_at 6.06320248
1316_at 4.780605117
1320_at 4.638800724
1405_i_at 5.787562947
1431_at 3.969820481
1438_at 7.097661381
1487_at 7.42727656
1494_f_at 4.819372836
1552256_a_at 7.287904684
1552257_a_at 7.165122367
1552258_at 4.040576272
1552261_at 4.616396634
1552263_at 5.070653678
1552264_a_at 6.384308238
1552266_at 4.035315837

Total number of rows: 54675

Table truncated, full table size 1211 Kbytes.




Supplementary file Size Download File type/resource
GSM452198.CEL.gz 5.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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