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Sample GSM752551 Query DataSets for GSM752551
Status Public on Jul 01, 2011
Title PBMC_epimutationpatientII5_rep1
Sample type genomic
 
Source name Peripheral blood lymphocytes, cancer-affected carrier
Organism Homo sapiens
Characteristics gender: female
phenotype: cancer-affected carrier of constitutional MLH1 epimutation
family member: II5
family relationship: proband
cell type: peripheral blood lymphocytes
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted from peripheral blood lymphocytes (PBL) and lymphoblastoid cell lines (LCL) using the phenol-chloroform method.
Label biotin
Label protocol Affymetrix® Genome-Wide Human SNP Nsp/Sty 6.0 User Guide (P/N 702504, Rev 3).
 
Hybridization protocol Affymetrix® Genome-Wide Human SNP Nsp/Sty 6.0 User Guide (P/N 702504, Rev 3).
Scan protocol Affymetrix® Genome-Wide Human SNP Nsp/Sty 6.0 User Guide (P/N 702504, Rev 3), GCFS 450, GCS 3000 HR, AGCC v3.0.
Description II5 from Lynch syndrome family 16.
Data processing APT v.1.12.0 used for preprocessing. Genotypes determined with apt-probeset-genotype (v. 1.264.2.2) using birdseed-v2 and cn-probe-chrXY-ratio for gender estimation. Intensity probe values extracted using apt-probeset-summarize (v. 1.178) with quant-norm.sketch=0, pm-only, med-polish, expr.genotype=true. The target distributions used for quantile normalization were separately generated on 300 WTCCC control samples (150 58BC and 150 NBS). Data was processed with the PennCNV-Affy routines to yield the 'GSE30348_gw6.lrr_baf.txt' file, which is linked to the Series GSE30348 record as a supplementary file. CNV calling with QuantiSNP, PennCNV and COKGEN.
 
Submission date Jun 30, 2011
Last update date Jul 01, 2011
Contact name Megan P Hitchins
E-mail(s) m.hitchins@unsw.edu.au
Phone 61293851431
Fax 61293851430
Organization name University of New South Wales
Department Lowy Cancer Research Centre
Lab Adult Cancer Program
Street address Randwick High Street
City Sydney
State/province NSW
ZIP/Postal code 2052
Country Australia
 
Platform ID GPL6801
Series (1)
GSE30348 Dominant MLH1 epimutation linked to 5'UTR variant c.-27C>A

Data table header descriptions
ID_REF
VALUE Log R Ratio
B_Allele_Freq B-allele frequency

Data table
ID_REF VALUE B_Allele_Freq
SNP_A-2131660 -0.1860 1.0000
SNP_A-1967418 -0.1358 0.9787
SNP_A-1969580 -0.3789 1.0000
SNP_A-4263484 0.2526 0.9807
SNP_A-1978185 0.0575 0.0000
SNP_A-4264431 0.3689 0.4040
SNP_A-1980898 -0.2426 1.0000
SNP_A-1983139 0.2804 0.0491
SNP_A-4265735 0.9942 0.0000
SNP_A-1995832 0.2244 0.0000
SNP_A-1995893 0.0973 0.0401
SNP_A-1997896 0.0342 0.0161
SNP_A-1997922 0.2831 0.0255
SNP_A-2000230 -0.1256 0.0904
SNP_A-2000332 0.2051 0.5113
SNP_A-2000337 -0.6141 0.0309
SNP_A-4268173 0.0006 0.5023
SNP_A-2002663 -0.4479 0.5576
SNP_A-2004169 -0.0844 0.4581
SNP_A-2004249 0.6782 1.0000

Total number of rows: 1757318

Table truncated, full table size 40949 Kbytes.




Supplementary file Size Download File type/resource
GSM752551.CEL.gz 26.7 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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