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Sample GSM614420 Query DataSets for GSM614420
Status Public on Nov 02, 2011
Title MD40-T180
Sample type RNA
 
Source name breast cancer tissue, patient MD40, RNAlater, 180 min ischemic time
Organism Homo sapiens
Characteristics patient id: MD40
stabilization: RNAlater
extra_cold_ischemic_time_min: 180
true_cold_ischemic_time_min: 215
passedqc: Y
rna_integrity_number (as reported by the agillent bioanalyzer): 8
rna_concentration_ngpul: 687
rna_260_280: 2.02
Treatment protocol Fresh tissue surgical excision specimens from breast cancer collected at time of surgery. The tissue was then cut into pieces of 1-2 mm in a petri dish using a sterile blade, mixed, and divided into 8 equal portions. A portion was placed into 1.5 ml RNAlater RNA stabilization reagent (Ambion, Inc., Austin TX) at baseline and 20, 40, 60, 120, and 180 minutes thereafter, or snap frozen in dry ice in a pre-chilled sample vial at baseline and 40 minutes thereafter. The time that each tissue portion was placed into contact with RNAlater solution or in the pre-chilled vial was recorded. Samples were stored at -70°C until RNA extraction.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from tissue using Qiagen Rneasy columns
Label biotin
Label protocol A single-round T7 amplification was used to generate biotin-labeled cRNA for hybridization. At least 1 ug of RNA is required for cRNA synthesis.
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized overnight at 46C on Affymetrix U133A arrays. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the diagnostic-grade Affymetrix scanner 3000DX
Data processing Probe intensities were quantified with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings. CEL files were normalized using global scaling with a trimmed mean target intensity of each array arbitrarily set to 600 using the MAS5 algorithm from the simpleaffy package (http://bioconductor.org/packages/2.4/bioc/html/simpleaffy.html).
 
Submission date Oct 29, 2010
Last update date Nov 02, 2011
Contact name Christos Hatzis
E-mail(s) [email protected]
Phone 781-938-3830
URL http://www.nuverabio.com
Organization name Nuvera Biosciences
Street address 400 West Cummings Park, Suite 5350
City Woburn
State/province MA
ZIP/Postal code 01801
Country USA
 
Platform ID GPL96
Series (1)
GSE25011 Study for evaluating the effect of cold ischemic time and RNA stabilization method on RNA integrity and gene expression measurements

Data table header descriptions
ID_REF
VALUE MAS5.0 signal intensity for each array was log2 transformed and scaled to a reference distribution of 1322 breast cancer specific genes.

Data table
ID_REF VALUE
1007_s_at 12.52360131
1053_at 8.375764435
117_at 8.421090224
121_at 10.82295922
1255_g_at 7.122383555
1294_at 9.625657674
1316_at 8.473794951
1320_at 4.599578111
1405_i_at 12.92841162
1431_at 6.986151354
1438_at 10.00555011
1487_at 8.922189487
1494_f_at 9.335946647
1598_g_at 11.56535918
160020_at 11.22182943
1729_at 10.00129833
177_at 7.757741815
1773_at 7.777287382
179_at 10.30514317
1861_at 7.115992475

Total number of rows: 22283

Table truncated, full table size 496 Kbytes.




Supplementary file Size Download File type/resource
GSM614420.CEL.gz 2.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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