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Sample GSM187730 Query DataSets for GSM187730
Status Public on May 31, 2007
Title PAD_00274_sample 11_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 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 921.247 P 0.000296708
AFFX-BioB-M_at 1583.38 P 4.42873e-05
AFFX-BioB-3_at 947.259 P 4.42873e-05
AFFX-BioC-5_at 2613.88 P 5.16732e-05
AFFX-BioC-3_at 3257.04 P 4.42873e-05
AFFX-BioDn-5_at 6580.15 P 4.42873e-05
AFFX-BioDn-3_at 11814.1 P 4.42873e-05
AFFX-CreX-5_at 38265.9 P 5.16732e-05
AFFX-CreX-3_at 46627.3 P 4.42873e-05
AFFX-DapX-5_at 317.9 P 9.4506e-05
AFFX-DapX-M_at 1048.53 P 0.000753643
AFFX-DapX-3_at 2046.14 P 7.00668e-05
AFFX-LysX-5_at 74.5954 P 0.036569
AFFX-LysX-M_at 184.935 M 0.0584438
AFFX-LysX-3_at 541.858 P 6.02111e-05
AFFX-PheX-5_at 57.8993 P 0.00844047
AFFX-PheX-M_at 168.662 P 0.0012475
AFFX-PheX-3_at 245.691 P 0.00110197
AFFX-ThrX-5_at 55.5582 A 0.39692
AFFX-ThrX-M_at 113.34 P 0.00933229

Total number of rows: 54675

Table truncated, full table size 1636 Kbytes.




Supplementary file Size Download File type/resource
GSM187730.CEL.gz 4.5 Mb (ftp)(http) CEL
GSM187730.CHP.gz 7.1 Mb (ftp)(http) CHP
Processed data provided as supplementary file

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