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Sample GSM480474 Query DataSets for GSM480474
Status Public on Feb 26, 2010
Title case 11 microRNA
Sample type RNA
 
Source name GCT patient case
Organism Homo sapiens
Characteristics tissue: primary intracranial pediatric germ cell tumor (GCT)
diagnosis: immature teratoma predominant + embryonal carcinoma + yolk sac tumor
age: 7.7 years
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 1 ug RNA using the One-Color Low RNA Input Linear Amplification PLUS kit (Agilent) according to the manufacturer's instructions, followed by RNeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 1.5 ug of Cy3-labelled cRNA (specific activity >10.0 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 250 ml containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 250 ml of 2x Agilent hybridization buffer was added to the fragmentation mixture and hybridized to Agilent Whole Human Genome Oligo Microarrays (G4112A) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried immediately by brief centrifugation.
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505B) using one color scan setting for 1x44k array slides (Scan Area 61x21.6 mm, Scan resolution 10um, Dye channel is set to Green and Green PMT is set to 100%).
Description miRNA expression data from CNS GCT patient
Data processing The scanned images were analyzed with Feature Extraction Software 9.1 (Agilent) using default parameters (protocol GE1-v1_91 and Grid: 012391_D_20060331) to obtain background subtracted and spatially detrended Processed Signal intensities. Features flagged in Feature Extraction as Feature Non-uniform outliers were excluded.
 
Submission date Dec 07, 2009
Last update date Feb 26, 2010
Contact name Yu Hsuan Wu
E-mail(s) [email protected]
Organization name National Yang-Ming University
Street address No.155, Sec.2, Linong Street
City Taipei
ZIP/Postal code 112
Country Taiwan
 
Platform ID GPL8227
Series (2)
GSE19347 microRNA expression data from pediatric primary intracranial germ cell tumor
GSE19350 Array-based bioinformatic analysis on pediatric primary central nervous system germ cell tumors

Data table header descriptions
ID_REF
VALUE Log2 transformed normalized signal intensity

Data table
ID_REF VALUE
SCorner3 2.321928
dmr_285 2.321928
dmr_3 2.321928
dmr_31a 2.321928
ebv-miR-BART1-5p 2.321928
ebv-miR-BART10 2.321928
ebv-miR-BART11-3p 2.321928
ebv-miR-BART12 2.321928
ebv-miR-BART13 8.038639
ebv-miR-BART14 2.321928
ebv-miR-BART14* 2.321928
ebv-miR-BART15 2.321928
ebv-miR-BART16 2.7731144
ebv-miR-BART17-3p 2.321928
ebv-miR-BART17-5p 2.321928
ebv-miR-BART18-3p 2.321928
ebv-miR-BART19-3p 5.3771725
ebv-miR-BART19-5p 2.321928
ebv-miR-BART3 2.321928
ebv-miR-BART3* 2.321928

Total number of rows: 761

Table truncated, full table size 16 Kbytes.




Supplementary file Size Download File type/resource
GSM480474_T1143_FE_file.txt.gz 1.8 Mb (ftp)(http) TXT
GSM480474_T1143_GeneView.txt.gz 9.6 Kb (ftp)(http) TXT
Processed data included within Sample table

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