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Sample GSM187772 Query DataSets for GSM187772
Status Public on May 31, 2007
Title PAD_00306_sample 25_preparation A_replicate 3
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 25
AML with normal karyotype + other abnormalities
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 1250.1 P 0.000389797
AFFX-BioB-M_at 2056.64 P 4.42873e-05
AFFX-BioB-3_at 1111.26 P 8.14279e-05
AFFX-BioC-5_at 2730.87 P 5.16732e-05
AFFX-BioC-3_at 4536.35 P 4.42873e-05
AFFX-BioDn-5_at 8199 P 4.42246e-05
AFFX-BioDn-3_at 17444.6 P 4.42873e-05
AFFX-CreX-5_at 45822.8 P 5.16732e-05
AFFX-CreX-3_at 55771 P 4.42873e-05
AFFX-DapX-5_at 308.29 P 0.000195116
AFFX-DapX-M_at 975.931 P 0.0012475
AFFX-DapX-3_at 2050.79 P 7.00668e-05
AFFX-LysX-5_at 96.0092 P 0.0284573
AFFX-LysX-M_at 153.553 A 0.116113
AFFX-LysX-3_at 634.492 P 0.000169227
AFFX-PheX-5_at 112.885 P 0.000296708
AFFX-PheX-M_at 124.743 M 0.0584438
AFFX-PheX-3_at 429.405 P 0.000195116
AFFX-ThrX-5_at 120.618 A 0.108979
AFFX-ThrX-M_at 182.058 P 0.00255552

Total number of rows: 54675

Table truncated, full table size 1627 Kbytes.




Supplementary file Size Download File type/resource
GSM187772.CEL.gz 4.4 Mb (ftp)(http) CEL
GSM187772.CHP.gz 7.2 Mb (ftp)(http) CHP
Processed data provided as supplementary file

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