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Sample GSM752552 Query DataSets for GSM752552
Status Public on Jul 01, 2011
Title PBMC_epimutationpatientI1_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: I1
family relationship: mother
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 I1 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 -0.0010 1.0000
SNP_A-1967418 -0.0350 0.9201
SNP_A-1969580 -0.3323 1.0000
SNP_A-4263484 0.1406 0.3857
SNP_A-1978185 0.0001 0.0210
SNP_A-4264431 -0.0108 0.0238
SNP_A-1980898 -0.3453 1.0000
SNP_A-1983139 0.0563 0.0165
SNP_A-4265735 1.0652 0.0000
SNP_A-1995832 0.1388 0.0255
SNP_A-1995893 0.1535 0.0594
SNP_A-1997896 -0.2003 0.0104
SNP_A-1997922 0.1265 0.0793
SNP_A-2000230 -0.2832 0.0342
SNP_A-2000332 0.2389 0.8564
SNP_A-2000337 -0.5857 0.0832
SNP_A-4268173 -0.1042 0.5069
SNP_A-2002663 -0.2882 0.0000
SNP_A-2004169 0.0398 0.5274
SNP_A-2004249 0.4022 0.5484

Total number of rows: 1757318

Table truncated, full table size 40942 Kbytes.




Supplementary file Size Download File type/resource
GSM752552.CEL.gz 26.9 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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