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Sample GSM1416557 Query DataSets for GSM1416557
Status Public on Jun 19, 2014
Title lung_30
Sample type RNA
 
Source name Right Upper Lobe
Organism Homo sapiens
Characteristics gender: M
histology: 869. Squamous Cell Carcinoma, NOS
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 7.505891067
AFFX-BioB-5_at 7.032094192
AFFX-BioB-M_at 7.422961964
AFFX-BioC-3_at 10.86378218
AFFX-BioC-5_at 11.02610889
AFFX-BioDn-3_at 13.38353816
AFFX-BioDn-5_at 12.49938972
AFFX-BkGr-GC03_at 1.340632225
AFFX-BkGr-GC04_at 1.312045187
AFFX-BkGr-GC05_at 1.331901781
AFFX-BkGr-GC06_at 1.358669847
AFFX-BkGr-GC07_at 1.370831692
AFFX-BkGr-GC08_at 1.413626247
AFFX-BkGr-GC09_at 1.450588435
AFFX-BkGr-GC10_at 1.525087566
AFFX-BkGr-GC11_at 1.580523012
AFFX-BkGr-GC12_at 1.658727469
AFFX-BkGr-GC13_at 1.805994996
AFFX-BkGr-GC14_at 2.074563991
AFFX-BkGr-GC15_at 2.557275003

Total number of rows: 60607

Table truncated, full table size 1883 Kbytes.




Supplementary file Size Download File type/resource
GSM1416557_LUNG3-30.CEL.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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