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Sample GSM187729 Query DataSets for GSM187729
Status Public on May 31, 2007
Title PAD_00266_sample 11_preparation B
Sample type RNA
 
Source name White blood human cells
Organism Homo sapiens
Characteristics Leukemia samples
Bone Marrow sample
Treatment protocol White blood cells were isolated through Ficoll-Hypaque density gradient centrifugation (for ALL samples) or through hemolysis (for AML samples)
Extracted molecule total RNA
Extraction protocol Lysis of the mononuclear cells followed by lysate homonogenization using a biopolymer shredding system in a microcentrifuge spin-column format followed by total RNA purification using selective binding columns (method A); Trizol extraction of total RNA was performed according to the manufacturer's instructions (method B); Trizol extraction of total RNA followed by purification step was performed according to the manufacturer's instructions (method C).
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 2 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 11 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome U133 Plus 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450DX.
Scan protocol GeneChips were scanned using the Scan GCS3000Dx.
Description Gene expression data from pediatric acute leukemia samples at diagnosis
Patient 11
ALL with t(12;21)
Data processing The data were analyzed using R software [www.r-project.org] with BioConductor package [www.bioconductor.org] and Partek Genomics Suite software [www.partek.com].
 
Submission date May 08, 2007
Last update date Nov 14, 2018
Contact name Andrea Zangrando
E-mail(s) [email protected]
Organization name University of Padova
Department Woman and Child's Health
Lab Hemato-Oncology
Street address Via Giustiniani, 3
City Padova
ZIP/Postal code 35138
Country Italy
 
Platform ID GPL570
Series (1)
GSE7757 Robustness of gene expression signatures in leukemia: comparison of three distinct total RNA preparation procedures.
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE119087
Reanalyzed by GSE122511

Data table header descriptions
ID_REF
VALUE MAS5.0-calculated signal intensity
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 868.217 P 0.000509415
AFFX-BioB-M_at 1511.31 P 4.42873e-05
AFFX-BioB-3_at 1003.82 P 4.42873e-05
AFFX-BioC-5_at 2677.67 P 5.16732e-05
AFFX-BioC-3_at 3426.97 P 4.42873e-05
AFFX-BioDn-5_at 7166.55 P 4.42873e-05
AFFX-BioDn-3_at 12299.6 P 5.16732e-05
AFFX-CreX-5_at 41931.9 P 5.16732e-05
AFFX-CreX-3_at 48385.9 P 4.42873e-05
AFFX-DapX-5_at 283.667 P 0.000146581
AFFX-DapX-M_at 931.568 P 0.000753643
AFFX-DapX-3_at 2041.24 P 6.02111e-05
AFFX-LysX-5_at 75.7936 P 0.0336773
AFFX-LysX-M_at 159.193 P 0.0336773
AFFX-LysX-3_at 660.103 P 0.000126798
AFFX-PheX-5_at 51.9119 P 0.036569
AFFX-PheX-M_at 143.022 P 0.0200219
AFFX-PheX-3_at 240.966 P 0.000224668
AFFX-ThrX-5_at 46.5091 A 0.368438
AFFX-ThrX-M_at 108.584 P 0.00499819

Total number of rows: 54675

Table truncated, full table size 1638 Kbytes.




Supplementary file Size Download File type/resource
GSM187729.CEL.gz 4.5 Mb (ftp)(http) CEL
GSM187729.CHP.gz 7.1 Mb (ftp)(http) CHP
Processed data provided as supplementary file

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