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Sample GSM615486 Query DataSets for GSM615486
Status Public on Jun 03, 2011
Title Colorectal Adenocarinoma 14837
Sample type genomic
 
Source name genomic DNA from colorectal adenocarcinoma 14837
Organism Homo sapiens
Characteristics sample type: Fresh Frozen tissue
disease state: Adenocarcinoma
gender: Female
tumor subsite: Distal
tissue source site: The ontario tumor bank network,Canada
batch: Batch 1
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted using Trizol reagent according to the manufacturer’s protocol.
Label Cy5 and Cy3
Label protocol standard Illumina label protocol
 
Hybridization protocol Bisulfite converted DNA was amplified, fragmented and hybridized to Illumina Infinium Human Methylation27k Beadchip using standard Illumina protocol.
Scan protocol Beadchips were imaged using Illumina BeadArray Reader using standard recommended Illumina scanner setting.
Data processing Mean non-background corrected signal intensities of the methylated (M) and unmethylated (U) for each CpG locus were extracted using the Illumina BeadStudio software v3.2. We masked data point as “NA” for the following conditions; 1) Probes containing single-nucleotide polymorphisms (SNPs), 2) those that overlap with a repetitive element that covers the targeted CpG dinucleotide, 3) those that overlap with regions of insertions and deletions in the human genome. Beta values with detection P value greater than 0.05 were also replaced as "NA". Furthermore, probes containing at least one “NA” across the tumor sample set were masked as “NA”. Beta values were normalized to eliminate the batch effects. Briefly, the batch means of beta values were brought closer to the overall mean while retaining the original range of DNA methylation data (0 to 1). We used only the tumor samples to calculate the batch means and overall mean in estimating the scaling factor for each batch.
Beta value was calculated as M/(M+U). Detection P values were obtained using the Z-score formula as previously described (Noushmehr et al., 2010, Cancer Cell). Detection P values that are less than 1.11e-16 are represented as 0.
 
Submission date Nov 01, 2010
Last update date Jun 03, 2011
Contact name Toshinori Hinoue
E-mail(s) thinoue@usc.edu
Phone 323-442-7458
Organization name USC Epigenome Center
Street address 1450 Biggy Street, NRT G511
City Los Angeles
State/province CA
ZIP/Postal code 90033-9601
Country USA
 
Platform ID GPL8490
Series (1)
GSE25062 Genome-scale analysis of aberrant DNA methylation in colorectal cancer

Data table header descriptions
ID_REF
VALUE normalized beta value

Data table
ID_REF VALUE
cg00000292 0.604373204
cg00002426 0.164045268
cg00003994 0.37572943
cg00005847 0.667817077
cg00006414 null
cg00007981 0.024778943
cg00008493 0.967342282
cg00008713 0.037250541
cg00009407 0.063065082
cg00010193 0.568301093
cg00011459 0.854906702
cg00012199 0.022693459
cg00012386 0.017418722
cg00012792 0.017040508
cg00013618 null
cg00014085 0.022704649
cg00014837 null
cg00015770 0.477593801
cg00016968 0.428146368
cg00019495 0.120315321

Total number of rows: 27578

Table truncated, full table size 582 Kbytes.




Supplementary file Size Download File type/resource
GSM615486.txt.gz 406.5 Kb (ftp)(http) TXT
Processed data included within Sample table

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