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Sample GSM187706 Query DataSets for GSM187706
Status Public on May 31, 2007
Title PAD_00250_sample 3_preparation C
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 3
T-ALL
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 1204.49 P 0.000258358
AFFX-BioB-M_at 1542.81 P 5.16732e-05
AFFX-BioB-3_at 758.874 P 9.4506e-05
AFFX-BioC-5_at 3563.44 P 4.42873e-05
AFFX-BioC-3_at 4150.75 P 4.42873e-05
AFFX-BioDn-5_at 6889.01 P 4.42873e-05
AFFX-BioDn-3_at 15812.7 P 4.42873e-05
AFFX-CreX-5_at 34318.6 P 5.16732e-05
AFFX-CreX-3_at 43748.5 P 4.42873e-05
AFFX-DapX-5_at 303.857 P 0.00159257
AFFX-DapX-M_at 1265.48 P 0.000972149
AFFX-DapX-3_at 2813.62 P 6.02111e-05
AFFX-LysX-5_at 32.2566 A 0.39692
AFFX-LysX-M_at 234 P 0.0284573
AFFX-LysX-3_at 606.822 P 0.000258358
AFFX-PheX-5_at 71.523 A 0.0726999
AFFX-PheX-M_at 184.499 P 0.0113844
AFFX-PheX-3_at 478.3 P 0.00359458
AFFX-ThrX-5_at 78.6525 A 0.250796
AFFX-ThrX-M_at 157.917 P 0.0138105

Total number of rows: 54675

Table truncated, full table size 1626 Kbytes.




Supplementary file Size Download File type/resource
GSM187706.CEL.gz 4.6 Mb (ftp)(http) CEL
GSM187706.CHP.gz 7.1 Mb (ftp)(http) CHP
Processed data provided as supplementary file

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