NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM412337 Query DataSets for GSM412337
Status Public on Nov 23, 2009
Title SCAN384_1
Sample type genomic
 
Source name Blood
Organism Homo sapiens
Characteristics tissue: Blood
phenotype: CLL sample
Extracted molecule genomic DNA
Extraction protocol Extraction of genomic DNA was performed using QIAamp DNA Mini kit (Qiagen) according to the manufacturer's instructions.
Label Total genomic DNA was digested with a restriction enzyme (Nsp1), ligated to an appropriate adapter for the enzyme, and subjected to PCR amplification using a single primer
Label protocol After digestion with DNase I, the PCR products were labeled with a biotinylated nucleotide analogue using terminal deoxynucleotidyl transferase and hybridized to the microarray
 
Hybridization protocol Hybridized probes were captured by streptavidin-phycoerythrin conjugates using Fluidics Station 450
Scan protocol GeneChip Scanner 3000 7G (Affymetrix Inc., Santa Clara, CA)
Description Array experiments were performed according to the standard protocols for Affymetrix GeneChip Mapping 250K arrays (Gene Chip Mapping 500K Assay Manual (P/N 701930 Rev2.), Affymetrix Inc., Santa Clara, CA).
Data processing QC, genotype calling and log2 ratios were produced in Affymetric Genotyping Console 3.0.1. The Dynamic Model (DM) algorithm was used to perform single sample QC. The QC specification for 250K is a Call Rate > 93
 
Submission date Jun 03, 2009
Last update date Nov 23, 2009
Contact name Anders Isaksson
E-mail(s) anders.isaksson@medsci.uu.se
Organization name Uppsala University
Street address Akademiska sjukhuset ing61 3tr
City Uppsala
ZIP/Postal code 75185
Country Sweden
 
Platform ID GPL3718
Series (1)
GSE16406 Copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia

Data table header descriptions
ID_REF
VALUE Genotyping Console metric for relative signal intensity
BAF B allele frequency

Data table
ID_REF VALUE BAF
SNP_A-1780270 -0.064708 0.0091941
SNP_A-1780272 0.2201 0.9401
SNP_A-1780285 0.067872 NaN
SNP_A-1780286 0.044193 0.54657
SNP_A-1780287 0.22449 -0.040142
SNP_A-1780289 -0.10154 0.99399
SNP_A-1780292 -0.00015297 0.85448
SNP_A-1780294 0.075562 0.41248
SNP_A-1780295 0.071044 0.86309
SNP_A-1780300 -0.17433 NaN
SNP_A-1780302 -0.21138 -0.049411
SNP_A-1780303 0.019405 NaN
SNP_A-1780304 0.03367 0.0047596
SNP_A-1780305 0.02973 0.50455
SNP_A-1780311 -0.13249 -0.23128
SNP_A-1780312 0.010628 0.12401
SNP_A-1780313 -0.23962 -0.050178
SNP_A-1780316 0.033361 0.76113
SNP_A-1780318 -0.055363 NaN
SNP_A-1780320 0.3279 0.9438

Total number of rows: 262217

Table truncated, full table size 7854 Kbytes.




Supplementary file Size Download File type/resource
GSM412337.CEL.gz 26.0 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap