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Sample GSM482508 Query DataSets for GSM482508
Status Public on Feb 18, 2010
Title Leukemia NOS cell line K562
Sample type genomic
 
Source name K562
Organism Homo sapiens
Characteristics cell type: Leukemia NOS cell line
cell line: K562
Growth protocol Cell lines were grown according to standard conditions.
Extracted molecule genomic DNA
Extraction protocol DNA was obtained from cell line pellets or tumors frozen at the time of surgical dissection and maintained at -80C until use, with the exception of 11 gliomas from which sufficiently high-quality DNA could be obtained from paraffin-embedded samples. The majority of tumors were obtained at primary surgery, with the exceptions of 27 prostate tumors obtained through rapid autopsy programs at the Universities of Washington and Michigan
Label Biotin
Label protocol As per manufacturer (Affymetrix)
 
Hybridization protocol Each sample was genotyped using the Sty I chip of the 500K Human Mapping Array wet (Affymetrix), containing probes to 238,270 SNP loci, according to manufacturer’s instructions. In brief, 250 ng of genomic DNA was digested with the StyI restriction enzyme (New England Biolabs), ligated to an adaptor with T4 ligase (New England Biolabs), and PCR-amplified using a 9700 Thermal Cycler I (Applied Biosystems) and Titanium Taq (Clontech) to achieve fragments ranging from 200-1100 bp. These fragments were pooled, concentrated, processed through a clean-up step, and further fragmented with DNaseI (Affymetrix) before being labeled, denatured, and hybridized to arrays
Scan protocol Arrays were washed and scanned using the GeneChip Scanner 3000 7G (Affymetrix)
Description Hybridized to 250K_Sty
Data processing Probe-level signal intensities were normalized to a common reference array using quantile normalization and combined to form SNP-level signal intensities using the dChip model-based expression (PM/MM) method . Genome-wide copy number estimates were obtained using tangent normalization, in which tumor signal intensities are divided by signal intensities from the linear combination of all normal samples that is most similar to the tumor (as described in Beroukhim et al, In Press; and Getz et al., In Preparation). Cancer samples were normalized against a pool of 1,480 reference samples derived from multiple studies; the code and reference data necessary to replicate this analysis are available for download in GEO. Genotype Call (SNP call) are provided in .CHP.TXT files: AA, AB, BB, NC, and NoCall.
 
Submission date Dec 09, 2009
Last update date Feb 18, 2010
Contact name Craig Mermel
E-mail(s) cmermel@broadinstitute.org
Phone 617-714-7563
Organization name Broad Institute
Department Cancer Program
Lab Matthew Meyerson Lab
Street address 7 Cambridge Center
City Cambridge
State/province MA
ZIP/Postal code 02142
Country USA
 
Platform ID GPL3720
Series (1)
GSE19399 Affymetrix 250K StyI SNP array data across multiple human cancer types

Data table header descriptions
ID_REF
VALUE copy number via tangent normalization

Data table
ID_REF VALUE
SNP_A-1909444 2.498095
SNP_A-2237149 2.301500
SNP_A-4303947 2.205263
SNP_A-2236359 2.423077
SNP_A-2205441 1.962507
SNP_A-2116190 1.974551
SNP_A-4291020 2.151889
SNP_A-2109914 2.096547
SNP_A-2291997 2.212280
SNP_A-4277872 1.763686
SNP_A-2118217 2.120709
SNP_A-1866065 2.684981
SNP_A-2288244 2.004660
SNP_A-1783407 1.965578
SNP_A-2169457 2.226728
SNP_A-4271011 2.223987
SNP_A-2082515 2.056307
SNP_A-1910751 1.918371
SNP_A-2081399 1.981934
SNP_A-2223642 2.037597

Total number of rows: 238230

Table truncated, full table size 5351 Kbytes.




Supplementary file Size Download File type/resource
GSM482508_PAVIN_p_STY33_Mapping250K_Sty_E06_128888.CEL.gz 28.1 Mb (ftp)(http) CEL
GSM482508_PAVIN_p_STY33_Mapping250K_Sty_E06_128888.CHP.TXT.gz 1.9 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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