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Sample GSM267514 Query DataSets for GSM267514
Status Public on May 31, 2008
Title Germ Cell Tumour, Histology 2, Biological replicate 7
Sample type RNA
Source name Yolk sac tumor
Organism Homo sapiens
Characteristics Pure, testicular, male, age 2, stage 2
Treatment protocol N/A
Growth protocol Fresh frozen tumor material (pre-chemotherapy) was provided by the individual banking centers across the UK and from Düsseldorf, Germany
Extracted molecule total RNA
Extraction protocol TRIzol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Total RNA from each sample was used to prepare biotinylated target RNA in a one-cycle target labeling procedure, with minor modifications from the manufacturer’s recommendations available at: Briefly, 10 µg of cleaned total RNA was used to generate first-strand cDNA by using a T7-linked oligo(dT) primer. After second-strand synthesis, in vitro transcription was performed with biotinylated UTP and CTP (Enzo Diagnostics), resulting in approximately 10-fold amplification of RNA.
Hybridization protocol Target cRNA generated from each sample were then processed as per manufacturer's recommendation using an Affymetrix GeneChip Instrument System ( at Geneservice Ltd (Cambridge Science Park, Cambridge, UK), formerly MRC Geneservice. Briefly, spike controls were added to 15 µg fragmented cRNA before overnight hybridization with the Genechip Human Genome U133A arrays (Affymetrix).
Scan protocol Arrays were then washed and stained with streptavidin-phycoerythrin, before being scanned on an Affymetrix GeneChip scanner.
Description Gene expression data from malignant germ cell tumor
Data processing The array, once scanned, was used to generate an image file (with the extension .dat). GeneChip Operating Software (GCOS) was then used to compute cell intensity data from the image file and this data was saved in a file with the extension .cel. The .cel (CEL) files were provided by Geneservice Ltd and used for subsequent data analysis. Pre-processing of microarray data (including background correction and normalization) relied on the Robust Multi-Array Average (RMA) method within R.
Submission date Feb 22, 2008
Last update date Apr 24, 2008
Contact name Roger David Palmer
Phone 0044 1223 763279
Fax 0044 1223 763284
Organization name Hutchison/MRC Research Centre
Department MRC Cancer Cell Unit
Lab 2.5
Street address Box 197 Hills Road
City Cambridge
ZIP/Postal code CB2 0XZ
Country United Kingdom
Platform ID GPL96
Series (1)
GSE10615 Pediatric malignant germ cell tumors show characteristic transcriptome profiles
Reanalyzed by GSM453851
Reanalyzed by GSE18155

Data table header descriptions
VALUE Post RMA normalization values

Data table
1007_s_at 8.772598998
1053_at 6.824024657
117_at 6.202003133
121_at 8.345950008
1255_g_at 4.262992524
1294_at 6.781762504
1316_at 5.601071642
1320_at 5.690848749
1405_i_at 4.330406615
1431_at 4.003538546
1438_at 7.761102617
1487_at 7.572969056
1494_f_at 6.409521909
1598_g_at 9.906300547
160020_at 8.41201001
1729_at 7.153968535
177_at 5.316878046
1773_at 6.409091743
179_at 8.673198169
1861_at 6.818641822

Total number of rows: 22283

Table truncated, full table size 496 Kbytes.

Supplementary file Size Download File type/resource
GSM267514.cel.gz 3.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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