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Sample GSM472633 Query DataSets for GSM472633
Status Public on Dec 01, 2009
Title AML_132_D_Nsp
Sample type genomic
 
Source name bone marrow
Organism Homo sapiens
Characteristics sample: Acute myeloid leukemia diagnosis sample
cell type: mononuclear cells
disease state: Acute myeloid leukemia
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted from mononuclear cells preparations obtained from peripheral blood using using the Qiagen ALL-Prep DNA/RNA Kit. DNA quality and quantity was assessed using a Nanodrop Spectrophotometer.
Label Biotin
Label protocol As per manufacturer (Affymetrix)
 
Hybridization protocol DNA was restriction digested, PCR amplified, fragmented, labeled and hybridized to each array according to the manufacturer's instructions.
Scan protocol The Arrays were then washed using Affymetrix fluidics stations, and scanned using the Gene Chip Scanner 3000.
Description Hybridized to 250K_Nsp
Genotype Call (SNP call): AA, AB, BB, NC, and NoCall; 'Signal' = Summarized signal
Data processing 1) CEL files and CHP files (generated by Affymetrix GTYPE) were processed by Copy Number Analyzer for GeneChip (CNAG) version 2.0 software or 2)CEL files and TXT files (generated by Affymetrix GTYPE using the DM algorithm) were processed by dChip and model-based expression performed using the PM/MM model. Normalization was performed using the reference normalization algorithm developed at St Jude and described in Mullighan et al Nature 2007;446:758. Normalization was performed against bone marrow or peripheral blood samples at remission from the same patient (paired analysis).
 
Submission date Nov 18, 2009
Last update date Nov 30, 2009
Contact name Jan Kroenke
E-mail(s) jankroenke@gmx.de
Organization name University Hospital of Ulm
Department Department of Internal Medicine III
Lab Molecular Genetics of Myeloid Leukemia
Street address Albert-Einstein-Allee 23
City Ulm
ZIP/Postal code 89081
Country Germany
 
Platform ID GPL3718
Series (1)
GSE19101 Identification of Acquired Copy Number Alterations and Uniparental Disomies in Cytogenetically Normal AML

Data table header descriptions
ID_REF
VALUE Genotypes: AA, AB, BB, No Call
CONFIDENCE
RAS1 Relative allele signal for the data in the first probe group
RAS2 Relative allele signal for the data in the second probe group
P-VALUE AA
P-VALUE AB
P-VALUE BB
P-VALUE NO CALL

Data table
ID_REF VALUE CONFIDENCE RAS1 RAS2 P-VALUE AA P-VALUE AB P-VALUE BB P-VALUE NO CALL
AFFX-5Q-123 No Call 0 0 0 0 0 0 0
AFFX-5Q-456 No Call 0 0 0 0 0 0 0
AFFX-5Q-789 No Call 0 0 0 0 0 0 0
AFFX-5Q-ABC No Call 0 0 0 0 0 0 0
AFFX-barcodeA No Call 0 0 0 0 0 0 0
AFFX-barcodeB No Call 0 0 0 0 0 0 0
AFFX-barcodeC No Call 0 0 0 0 0 0 0
AFFX-barcodeD No Call 0 0 0 0 0 0 0
AFFX-barcodeE No Call 0 0 0 0 0 0 0
AFFX-barcodeF No Call 0 0 0 0 0 0 0
AFFX-barcodeG No Call 0 0 0 0 0 0 0
AFFX-barcodeH No Call 0 0 0 0 0 0 0
AFFX-barcodeI No Call 0 0 0 0 0 0 0
AFFX-barcodeJ No Call 0 0 0 0 0 0 0
AFFX-barcodeK No Call 0 0 0 0 0 0 0
AFFX-barcodeL No Call 0 0 0 0 0 0 0
AFFX-barcodeM No Call 0 0 0 0 0 0 0
AFFX-barcodeN No Call 0 0 0 0 0 0 0
AFFX-barcodeO No Call 0 0 0 0 0 0 0
AFFX-barcodeP No Call 0 0 0 0 0 0 0

Total number of rows: 262338

Table truncated, full table size 20220 Kbytes.




Supplementary file Size Download File type/resource
GSM472633_AML_132_D_Nsp.CEL.gz 22.3 Mb (ftp)(http) CEL
GSM472633_AML_132_D_Nsp.CHP.gz 661.9 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data are available on Series record

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