NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1416609 Query DataSets for GSM1416609
Status Public on Jun 19, 2014
Title lung_82
Sample type RNA
 
Source name Left Upper Lobe
Organism Homo sapiens
Characteristics gender: M
histology: 105. Adenocarcinoma, 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 7.316975375
AFFX-BioB-5_at 6.913878865
AFFX-BioB-M_at 7.324634738
AFFX-BioC-3_at 10.78122849
AFFX-BioC-5_at 10.9007652
AFFX-BioDn-3_at 13.35600834
AFFX-BioDn-5_at 12.48486364
AFFX-BkGr-GC03_at 1.501616412
AFFX-BkGr-GC04_at 1.32790464
AFFX-BkGr-GC05_at 1.37918437
AFFX-BkGr-GC06_at 1.399301734
AFFX-BkGr-GC07_at 1.430832736
AFFX-BkGr-GC08_at 1.427896496
AFFX-BkGr-GC09_at 1.467943943
AFFX-BkGr-GC10_at 1.524967588
AFFX-BkGr-GC11_at 1.55848846
AFFX-BkGr-GC12_at 1.631762964
AFFX-BkGr-GC13_at 1.738756348
AFFX-BkGr-GC14_at 1.966691929
AFFX-BkGr-GC15_at 2.435541873

Total number of rows: 60607

Table truncated, full table size 1883 Kbytes.




Supplementary file Size Download File type/resource
GSM1416609_LUNG3-82.CEL.gz 4.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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