NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM280898 Query DataSets for GSM280898
Status Public on Jun 24, 2008
Title Training_Site2_03
Sample type RNA
 
Source name HEPG2
Organism Homo sapiens
Characteristics HepG2 (liver carcinoma) cell line
input total RNA (ug) = 1ug; cRNA yield (ug) = 9.97694; Lot# = 035PO41658D
Extracted molecule total RNA
Extraction protocol The eight samples that were analysed during the training course were represented by MCF-7 (breast adenocarcinoma) and HepG2 (liver carcinoma) cell line total RNA (Ambion, Austin, TX, USA) with 1.0 µg to 8.0 µg input of total RNA (for labeling described below), and four leukaemia patient sample lysates prepared from mononuclear cells obtained after Ficoll density purification.
The total RNA from the patient lysates was extracted at each centre as part of the training program, making these samples a test of the entire microarray process workflow post sample acquisition (RNeasy kit, Qiagen, Hilden, Germany).
Label biotin
Label protocol For each sample preparation, total RNA was converted into double-stranded cDNA by reverse transcription using a cDNA Synthesis System kit including an oligo(dT)24 – T7 primer(Roche Applied Science, Mannheim, Germany) and Poly-A control transcripts (Affymetrix, Santa Clara, CA, USA).
The generated cRNA was purified using the GeneChip Sample Cleanup Module (Affymetrix) and quantified using the NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).
The incubation steps during the cDNA synthesis, in vitro transcription reaction, and target fragmentation were performed using the Hybex Microarray Incubation System (SciGene, Sunnyvale, CA, USA) and Eppendorf ThermoStat plus instruments (Eppendorf, Hamburg, Germany).
 
Hybridization protocol Hybridization, washing, and staining protocols, respectively, were performed on Affymetrix GeneChip instruments (Hybridization Oven 640, Fluidics Station FS450) as recommended by the manufacturer.
Scan protocol Scanning was performed on Affymetrix GeneChip Scanner GCS3000 as recommended by the manufacturer.
Description Performed by Operator 1 from Site2 at Training stage
Data processing Data pre-processing included the summarization to generate probe set level signals for each microarray experiment and was performed using DQN algorithm.
 
Submission date Apr 10, 2008
Last update date Aug 28, 2018
Contact name Rachel Li
E-mail(s) [email protected]
Phone 925 730-8136
Organization name Roche
Street address 4300 Hacienda Dr.
City Pleasanton
State/province CA
ZIP/Postal code 94588
Country USA
 
Platform ID GPL570
Series (1)
GSE11135 The MILE (Microarray Innovations In LEukemia) study pre-phase
Relations
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE DS, DQN1 signal intensity

Data table
ID_REF VALUE
1007_s_at 0.325051
1053_at 0.243219
117_at 0.0873425
121_at 0.276792
1255_g_at 0.0812296
1294_at 0.21375
1316_at 0.22848
1320_at 0.0529692
1405_i_at 0.0111501
1431_at 0.0913673
1438_at 0.0713019
1487_at 0.345335
1494_f_at 0.17332
1598_g_at 0.141409
160020_at 0.25407
1729_at 0.242083
1773_at 0.178003
177_at 0.220167
179_at 0.216354
1861_at 0.194385

Total number of rows: 54613

Table truncated, full table size 1065 Kbytes.




Supplementary file Size Download File type/resource
GSM280898.CEL.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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