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Sample GSM331805 Query DataSets for GSM331805
Status Public on Sep 30, 2009
Title MILES stage 2 data N2_0073
Sample type RNA
 
Source name Leukemia patient sample
Organism Homo sapiens
Characteristics sample type: peripheral blood
leukemia class: CLL
Treatment protocol Samples are from untreated patients.
Growth protocol not applicable
Extracted molecule total RNA
Extraction protocol The total RNA was purified either with Qiagen RNeasy Mini kits (Qiagen, Hilden, Germany) or with TRIzol-based protocols
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 instruments as recommended by the manufacturer using default settings. The software used was GCOS 1.2 or higher.
Data processing Data pre-processing included a summarization and quantile normalization step to generate probe set level signal intensities for each microarray experiment and was performed as previously published by Liu WM et al. PQN and DQN: algorithms for expression microarrays. J.Theor.Biol. 2006;243:273-278.
 
Submission date Oct 12, 2008
Last update date Oct 07, 2011
Contact name Wei-Min Liu
E-mail(s) wei-min.liu@roche.com
Phone 9257308446
Organization name Roche Molecular Systems
Street address 4300 Hacienda Drive
City Pleasanton
State/province CA
ZIP/Postal code 94588
Country USA
 
Platform ID GPL7473
Series (2)
GSE13164 Microarray Innovations in LEukemia (MILE) study: Stage 2 data
GSE13204 Microarray Innovations in LEukemia (MILE) study

Data table header descriptions
ID_REF
VALUE_DS The signal used was DS, see Liu, W.-m., R. Li, J. Z. Sun, J. Wang, J. Tsai, W. Wen, A. Kohlmann, P. M. Williams, PQN and DQN: Algorithms for expression microarrays, J. Theoretical Biol., 243 (2006), 273-278.
ABS_CALL
DETECTION P-VALUE
VALUE The signal used was DQN3, i.e., DQN signal normalized with quantiles of the beta distribution with parameters p=1.2 and q=3, see Liu, W.-m., R. Li, J. Z. Sun, J. Wang, J. Tsai, W. Wen, A. Kohlmann, P. M. Williams, PQN and DQN: Algorithms for expression microarrays, J. Theoretical Biol., 243 (2006), 273-278.

Data table
ID_REF VALUE_DS ABS_CALL DETECTION P-VALUE VALUE
AFFX-HSAC07/X00351_3_at 5382.28 P 4.42873e-05
AFFX-HSAC07/X00351_5_at 1385.33 P 0.000753643
AFFX-HUMGAPDH/M33197_3_at 7771.71 P 4.42873e-05
AFFX-HUMGAPDH/M33197_5_at 5288.66 P 4.42873e-05
AFFX-r2-Bs-lys-3_at 39.7635 M 0.0561523
AFFX-r2-Bs-lys-5_at 14.0114 A 0.432373
AFFX-r2-Bs-phe-3_at 58.4843 A 0.0805664
AFFX-r2-Bs-phe-5_at 28.2752 A 0.219238
AFFX-r2-Bs-thr-3_s_at 55.1172 A 0.129639
AFFX-r2-Bs-thr-5_s_at 35.242 A 0.171387
AFFX-r2-Bs-dap-3_at 200.328 P 0.000732422
AFFX-r2-Bs-dap-5_at 100.201 P 0.00292969
AFFX-r2-Ec-bioC-3_at 34.0785 A 0.567627
AFFX-r2-Ec-bioC-5_at 9.21357 A 0.665527
AFFX-CreX-3_at 20.7464 A 0.814869
AFFX-CreX-5_at 4.95431 A 0.997444
AFFX-BioDn-3_at 24.4344 A 0.617401
AFFX-BioDn-5_at 5.41518 A 0.979978
AFFX-BioC-3_at 23.0154 A 0.41138
AFFX-BioC-5_at 15.6611 A 0.712257

Total number of rows: 1480

Table truncated, full table size 70 Kbytes.




Supplementary file Size Download File type/resource
GSM331805.CEL.gz 204.2 Kb (ftp)(http) CEL
Processed data included within Sample table

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