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Sample GSM853095 Query DataSets for GSM853095
Status Public on Apr 29, 2012
Title Papillary Type 1 sample 529
Sample type genomic
Source name Renal neoplasm, Papillary Type 1
Organism Homo sapiens
Characteristics gender: M
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was purified from frozen samples following the DNeasy Blood and Tissue Kit (Qiagen, Valencia, CA). Briefly, 0.25 mg of frozen tissue was placed in Qiagen buffer and Proteinase K (>600 mAU/ml) and incubated for 3 hours at 150 rpm. Following tissue lysis and protein removal, genomic DNA was eluted in 100µl of Buffer AE (Qiagen). Only samples with a spectrophotometric absorption ratio of 260/280 > 1.8 (Nanodrop ND-1000 spectrophotometer, NanoDrop , Wilmington, DE) were included in subsequent assays. Purified genomic DNA was evaluated using agarose gels (2%) or microfluidic chips (12000 DNA Chip, Bioanalyzer 2100, Agilent Technologies, Santa Clara, CA) to confirm that the DNA from each specimen was of high molecular weight (> 10Kb) with minimal detectable degradation.
Label biotin
Label protocol Sty I and Nsp I restriction enzymes (New England Biolabs, Ipswich, MA) were used to separately digest 250ng of DNA resulting in a total digest of 500 ng of whole genomic DNA per sample. Each sample was ligated with the appropriate adaptor (Sty or Nsp) provided in the Affymetrix 6.0 protocol and a total of seven PCR reactions were performed per sample (three Sty I restriction digest/ligation DNA reactions and four Nsp I restriction digest/ligation DNA reactions) and pooled into one tube with a total volume of 700µl. Purification of resulting PCR products was performed using the protocol associated with the Affymetrix Cytogenetics Copy Number Assay which required the use of Agencourt AMPure beads (Beckman Coulter, Danvers, MA). Each pooled sample was fragmented with DNAse1, biotinylated and end-labeled.
Hybridization protocol Samples were hybridized on Genome-Wide SNP 6.0 arrays for 18 hours at 500C with rotation (60 rpm) in an Affymetrix Gene Chip Hybridization Oven (Model 640).
Scan protocol Arrays were washed, stained and scanned according to the Affymetrix Genome-Wide SNP 6.0 protocol using the Affymetrix GeneChip Fluidics Station (Model 450), GeneChip Scanner 3000 7G, and GeneChip Command Console (v3.0.2) software.
Data processing The Affymetrix Genotyping Console (v3.0.2) was used to generate a SNP call for each probe set on each array. SNP calls were determined for an average of 96.78% (S.D.= 4.27%) of the array probe sets per specimen throughout the study. Affymetrix CEL and CHP files were transferred to Partek Genomics Suite v6.5 (Partek Inc, St Louis, MI) for copy number and loss of heterozygosity (LOH) analysis respectively. CEL files were imported using the default setting, which adjusts hybridized intensities based on fragment length and probe sequence. Copy number was generated by comparing the hybridized intensities of each array to the laboratory normal tissue reference set (n=31) eliminating inter-laboratory variability introduced by comparison to other databases such as the HapMap. Copy number measurements were smoothed based on local GC content using a 1 Mb window. Partek segmentation algorithm was used to identify regions of significant copy number variation (CNV) from normal consisting of a minimum of 30 genomic markers and p-value of less than .001, with signal to noise and expected range set to 0.3. The median length of inter-marker spacing on the SNP 6.0 array is 680 bp with a median length of a 30 marker region approximately 20Kb. Regions of LOH were identified for tumors with a matched normal pair (2 chromophobe, 1 clear cell, 1 papillary type 1, and 1 papillary type 2 sample) using the Hidden Markov Model in Partek Genomics Suite.
There is copy number data for each tumor sample supplied in the matrix. This copy number data was created using the laboratory unpaired normal reference set (available in CEL file format) and has been GC corrected.
Submission date Dec 22, 2011
Last update date Apr 29, 2012
Contact name John Michael Krill-Burger
Phone 412-656-6727
Organization name University of Pittsburgh Medical Center
Street address Rm. WG21.3 Shadyside Hospital
City Pittsburgh
State/province PA
ZIP/Postal code 15232
Country USA
Platform ID GPL6801
Series (1)
GSE34676 Renal Cell Neoplasms Contain Shared Tumor Type-Specific Copy Number Variations

Data table header descriptions
VALUE unpaired GC corrected copy number

Data table
AFFX-SNP_10000979 2.6338
AFFX-SNP_10009702 2.61377
AFFX-SNP_10015773 1.69455
AFFX-SNP_10021569 2.69164
AFFX-SNP_10026879 2.52314
AFFX-SNP_10029725 1.84963
AFFX-SNP_10034687 2.39013
AFFX-SNP_10036267 1.79213
AFFX-SNP_10037362 2.21111
AFFX-SNP_10037636 1.96805
AFFX-SNP_10039349 1.4712
AFFX-SNP_10039442 1.72724
AFFX-SNP_10039933 2.17511
AFFX-SNP_10046830 2.6696
AFFX-SNP_10047363 2.16542
AFFX-SNP_10047841 1.38323
AFFX-SNP_10049334 2.1509
AFFX-SNP_10052664 1.78304
AFFX-SNP_10057887 1.59285
AFFX-SNP_10064911 2.00616

Total number of rows: 1855448

Table truncated, full table size 36386 Kbytes.

Supplementary file Size Download File type/resource
GSM853095.CEL.gz 29.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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