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Sample GSM614406 Query DataSets for GSM614406
Status Public on Nov 02, 2011
Title MD57-T40-F (no RNAlater)
Sample type RNA
 
Source name breast cancer tissue, patient MD57, flash frozen, 40 min ischemic time
Organism Homo sapiens
Characteristics patient id: MD57
stabilization: FlashFrozen
extra_cold_ischemic_time_min: 40
true_cold_ischemic_time_min: 67
passedqc: Y
rna_integrity_number (as reported by the agillent bioanalyzer): 3.3
rna_concentration_ngpul: 201.9
rna_260_280: 2.09
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 12.95210798
1053_at 4.090732287
117_at 8.304268557
121_at 11.44398893
1255_g_at 6.969861601
1294_at 10.36796511
1316_at 9.185052415
1320_at 4.93818806
1405_i_at 8.513477024
1431_at 6.395649423
1438_at 5.820629328
1487_at 9.351163241
1494_f_at 9.932984243
1598_g_at 12.21817512
160020_at 10.90871878
1729_at 9.905716935
177_at 6.76663116
1773_at 5.55142182
179_at 11.24076939
1861_at 8.712292927

Total number of rows: 22283

Table truncated, full table size 496 Kbytes.




Supplementary file Size Download File type/resource
GSM614406.CEL.gz 2.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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