NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM614446 Query DataSets for GSM614446
Status Public on Nov 02, 2011
Title MD66-T20
Sample type RNA
 
Source name breast cancer tissue, patient MD66, RNAlater, 20 min ischemic time
Organism Homo sapiens
Characteristics patient id: MD66
stabilization: RNAlater
extra_cold_ischemic_time_min: 20
true_cold_ischemic_time_min: 66
passedqc: Y
rna_integrity_number (as reported by the agillent bioanalyzer): 6.4
rna_concentration_ngpul: 354.7
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) [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 11.84920582
1053_at 8.43127221
117_at 8.44667664
121_at 10.33541388
1255_g_at 5.454551949
1294_at 9.831539674
1316_at 7.900548931
1320_at 7.43893613
1405_i_at 8.610058452
1431_at 5.567842155
1438_at 9.629432667
1487_at 9.524142672
1494_f_at 8.791180049
1598_g_at 12.67964577
160020_at 11.70579098
1729_at 8.924547008
177_at 8.12405665
1773_at 8.203393478
179_at 10.54443876
1861_at 8.242067494

Total number of rows: 22283

Table truncated, full table size 496 Kbytes.




Supplementary file Size Download File type/resource
GSM614446.CEL.gz 2.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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