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Sample GSM1416550 Query DataSets for GSM1416550
Status Public on Jun 19, 2014
Title lung_23
Sample type RNA
 
Source name Right Upper Lobe
Organism Homo sapiens
Characteristics gender: M
histology: 709. Non-Small Cell
Extracted molecule total RNA
Extraction protocol Samples are processed in parallel in 96-well plates to minimize potential variation. Reaction purification is achieved using magnetic binding beads for cDNA and Qiagen RNeasy kits for cRNA purification. Isolated total RNA samples were assayed for quality (Agilent Bioanalyzer) and yield (Ribogreen) metrics prior to amplification.
Label biotin
Label protocol Samples were amplified and labeled using a custom automated version of the NuGEN Ovation v2 with WB (whole blood) reagents protocol (using Ribo-SPIA amplification). The labeled molecules are biotinylated-cRNA. Sample amplification and labeling were performed by LabCorp Clinical Trials-Genomic Services in Seattle, Washington.
 
Hybridization protocol GeneChip microarrays are loaded with the fragmented target sample/hybridization buffer mix using standard manual techniques. Arrays are hybridized for 18 hours at 45C with vigorous mixing. Unbound sample is removed and staining is accomplished through the binding of streptavidin conjugated phycoerythrin to the hybridized target. Excess label is removed. Washing and staining steps are performed by the Affymetrix FS450 fluidics station using standard protocols.
Scan protocol Arrays are scanned using a GeneChip Scanner 3000 7G with a 48 array autoloader. The scanner maintains the optimal temperature for the arrays prior to and during scanning.
Data processing Raw CEL files were normalized by RMA algorithm as implemented in the justRMA function in Bioconductor/R with default parameters.
 
Submission date Jun 19, 2014
Last update date Jun 19, 2014
Contact name Patrick Grossmann
E-mail(s) PATRICK@JIMMY.HARVARD.EDU
Organization name Dana-Farber Canacer Institute
Department Radiation Oncology
Lab Aerts Lab
Street address 450 Brookline Ave
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platform ID GPL15048
Series (1)
GSE58661 89 NSCLC patients with gene expression profiles and matching CT imaging data available at TCIA.

Data table header descriptions
ID_REF
VALUE Log2 normalized intensity values as generated by RMA algorithm

Data table
ID_REF VALUE
AFFX-BioB-3_at 7.866523317
AFFX-BioB-5_at 7.485122643
AFFX-BioB-M_at 7.808579855
AFFX-BioC-3_at 11.14286606
AFFX-BioC-5_at 11.24381804
AFFX-BioDn-3_at 13.46878578
AFFX-BioDn-5_at 12.65334166
AFFX-BkGr-GC03_at 1.369167983
AFFX-BkGr-GC04_at 1.338740515
AFFX-BkGr-GC05_at 1.357573963
AFFX-BkGr-GC06_at 1.383004771
AFFX-BkGr-GC07_at 1.39577081
AFFX-BkGr-GC08_at 1.401718981
AFFX-BkGr-GC09_at 1.4628406
AFFX-BkGr-GC10_at 1.516602364
AFFX-BkGr-GC11_at 1.611100708
AFFX-BkGr-GC12_at 1.743279268
AFFX-BkGr-GC13_at 1.885290779
AFFX-BkGr-GC14_at 2.252015848
AFFX-BkGr-GC15_at 2.821445478

Total number of rows: 60607

Table truncated, full table size 1883 Kbytes.




Supplementary file Size Download File type/resource
GSM1416550_LUNG3-23.CEL.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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