NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM850487 Query DataSets for GSM850487
Status Public on Dec 10, 2012
Title XY8
Sample type RNA
 
Source name NPC biopsy
Organism Homo sapiens
Characteristics disease state: nasopharyngeal carcinoma
Biomaterial provider Department of Pathology, Guangdong Medical College
Extracted molecule total RNA
Extraction protocol 8 micron cryosections were transferred onto PALM membrane slides (P.A.L.M. Microlaser Technologies) and air dried on ice for about 1 minute. Slides were immersed for 2 minutes in cold 75% ethanol, tapped dry and stained for 30 seconds in cold haematoxylin and eosin (9:1) containing 1% NucleoGuard (AmpTec, Hamburg). Excess stain was tapped off and slides were washed in cold nuclease-free water for 30 seconds, cold 75% ethanol for 1 minute, cold 100% ethanol for 1 minute then air dried. Tumour cells for analysis were excised by laser microdissection and pressure catapulting using a PALM MicroBeam instrument and caught on PALM Adhesive Caps. A minimum of 200,000 µm2 of tissue was collected for each DNA or RNA extraction. RNA was extracted by adding 100µl of RLT buffer (Qiagen) supplemented with 1µl of N-carrier (AmpTec) and 1 µl of NucleoGuard followed by incubation at room temperature for 15 minutes. Extracted RNA was cleaned up using a Qiagen RNeasy mini kit, including the on-column DNase step as per the manufacturer’s instructions.
Label biotin
Label protocol The eluted RNA was collected by ethanol precipitation in the presence of 1 µl P-carrier (AmpTec), washed twice with 80% ethanol and subjected to three rounds of amplification followed by biotin labelling using an ExpressArt TR Nano amplification kit (AmpTec) and an Affymetrix IVT labelling kit.
 
Hybridization protocol Biotinylated RNA was fragmented and hybridised to Affymetrix Human Genome U133Plus2 Arrays according to the Affymetrix protocol.
Scan protocol All arrays were washed and stained on an Affymetrix FS450 fluidics station then scanned using an Affymetrix GeneChip 3000 7G scanner as per Affymetrix procedures.
Data processing Expression array data were analysed with GCOS using the default settings except that the target signal was set to 100.
 
Submission date Dec 19, 2011
Last update date Dec 10, 2012
Contact name Wenbin Wei
E-mail(s) Wenbin.Wei2@durham.ac.uk
Organization name Durham University
Department Biosciences
Street address Stockton Road
City Durham
ZIP/Postal code DH1 3LE
Country United Kingdom
 
Platform ID GPL570
Series (1)
GSE34573 A Global View of the Oncogenic Landscape in Nasopharyngeal Carcinoma:An Integrated Analysis at the Genetic and Expression Levels

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 1003.38 P 0.000126798
AFFX-BioB-M_at 1525.82 P 5.16732e-05
AFFX-BioB-3_at 878.124 P 4.42873e-05
AFFX-BioC-5_at 3492.86 P 5.16732e-05
AFFX-BioC-3_at 4153.86 P 4.42873e-05
AFFX-BioDn-5_at 7902.38 P 4.42873e-05
AFFX-BioDn-3_at 9398.27 P 5.16732e-05
AFFX-CreX-5_at 33561.1 P 5.16732e-05
AFFX-CreX-3_at 37579.2 P 4.42873e-05
AFFX-DapX-5_at 41.7635 A 0.165861
AFFX-DapX-M_at 10.5864 A 0.631562
AFFX-DapX-3_at 41.3975 A 0.41138
AFFX-LysX-5_at 53.2937 A 0.175328
AFFX-LysX-M_at 16.424 A 0.645547
AFFX-LysX-3_at 30.0092 A 0.262827
AFFX-PheX-5_at 4.28494 A 0.979987
AFFX-PheX-M_at 2.99137 A 0.993129
AFFX-PheX-3_at 105.573 A 0.205732
AFFX-ThrX-5_at 9.25544 A 0.712257
AFFX-ThrX-M_at 25.6091 A 0.327079

Total number of rows: 54675

Table truncated, full table size 1597 Kbytes.




Supplementary file Size Download File type/resource
GSM850487.CEL.gz 4.5 Mb (ftp)(http) CEL
GSM850487.CHP.gz 494.0 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap