NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM614475 Query DataSets for GSM614475
Status Public on Nov 02, 2011
Title MD71-T0-F (no RNAlater)
Sample type RNA
 
Source name breast cancer tissue, patient MD71, flash frozen, 0 min ischemic time
Organism Homo sapiens
Characteristics patient id: MD71
stabilization: FlashFrozen
extra_cold_ischemic_time_min: 0
true_cold_ischemic_time_min: 46
passedqc: Y
rna_integrity_number (as reported by the agillent bioanalyzer): 7.1
rna_concentration_ngpul: 376.5
rna_260_280: 2.04
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) christos@nuverabio.com
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 12.05756184
1053_at 8.3990974
117_at 8.029262757
121_at 10.74373813
1255_g_at 4.824726162
1294_at 9.903163168
1316_at 7.922192006
1320_at 6.080277631
1405_i_at 10.73510799
1431_at 7.043366198
1438_at 8.582951397
1487_at 8.801456557
1494_f_at 9.08822678
1598_g_at 11.54830096
160020_at 10.71639033
1729_at 8.952259741
177_at 7.329196362
1773_at 7.618547259
179_at 10.19369855
1861_at 7.92192178

Total number of rows: 22283

Table truncated, full table size 496 Kbytes.




Supplementary file Size Download File type/resource
GSM614475.CEL.gz 2.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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