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Sample GSM752549 Query DataSets for GSM752549
Status Public on Jul 01, 2011
Title PBMC_epimutationpatientII4_rep1
Sample type genomic
 
Source name Peripheral blood lymphocytes, asymptomatic carrier
Organism Homo sapiens
Characteristics gender: female
phenotype: asymptomatic carrier of constitutional MLH1 epimutation
family member: II4
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 II4 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 -0.1273 0.9078
SNP_A-1967418 -0.1184 0.9794
SNP_A-1969580 -0.0333 0.8965
SNP_A-4263484 0.0254 1.0000
SNP_A-1978185 -0.1010 0.0131
SNP_A-4264431 -0.0901 0.5148
SNP_A-1980898 -0.5495 0.9587
SNP_A-1983139 -0.3952 0.0871
SNP_A-4265735 0.9671 0.0000
SNP_A-1995832 -0.2043 0.0764
SNP_A-1995893 0.0038 0.0458
SNP_A-1997896 -0.1982 0.0180
SNP_A-1997922 -0.3461 0.0715
SNP_A-2000230 0.1270 0.1235
SNP_A-2000332 0.3298 0.4737
SNP_A-2000337 -0.2677 0.0098
SNP_A-4268173 0.0564 1.0000
SNP_A-2002663 -0.2823 0.5444
SNP_A-2004169 -0.7022 0.8837
SNP_A-2004249 0.1674 0.5811

Total number of rows: 1757318

Table truncated, full table size 41069 Kbytes.




Supplementary file Size Download File type/resource
GSM752549.CEL.gz 27.6 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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