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Sample GSM554418 Query DataSets for GSM554418
Status Public on Oct 19, 2011
Title Breast cancer cell line R12C9
Sample type genomic
 
Source name Normal lymphoid cell line
Organism Homo sapiens
Characteristics conditions: Normal
treatment protocol: The R12C9 cells were harvested after 3 days of growth.
growth protocol: The normal CD4+ lymphoid cell line R12C9 was maintained in Isocove Dubelcco medium supplemented with 10% human serum HS54, L-Arginine, L-Asparagine, L-glutamine, 2-mercaptoéthanol and methyltryptophane as well as with 10 ng/mL of IL-7 and 50 U/mL of IL-2.
cell line: R12C9
methylation barcode: 5294239013_D
Treatment protocol Cells were harvested after 5 or 6 passages. They were detached from the culture flask using a cell scraper.
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted using the QIAamp DNA Mini Kit according to the supplier’s instructions (Qiagen, Hilden, Germany). This included the recommended proteinase K and RNase A digestions. DNA was quantitated with the NanoDrop® ND-1000 UV-Vis Spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).
Genomic DNA from cells was extracted using the QIAamp DNA Mini Kit according to the supplier’s instructions (Qiagen, Hilden, Germany). This included the recommended proteinase K and RNase A digestions. DNA was quantitated with the NanoDrop® ND-1000 UV-Vis Spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).
Label C-Bio and A-DNP
Label protocol Labelled nucleotides were added to extend the primers hybridized to the DNA and primers were stained according to the Infinium® Methylation Manual Protocol (Illumina, San Diego, USA).
 
Hybridization protocol DNA samples were hybridized onto the HumanMethylation27 BeadChips during 16 hours at 48°C. Unhybridized and non-specifically hybridized DNA were washed from the BeadChips, according to the Infinium® Methylation Manual Protocol (Illumina, San Diego, USA).
Scan protocol The BeadChips were scanned with the Illumina BeadArrayTM Reader.
Data processing Initial data analysis was performed with the Methylation module of the Genome Studio software provided by Illumina.
 
Submission date Jun 10, 2010
Last update date Oct 19, 2011
Contact name Benjamin Haibe-Kains
E-mail(s) benjamin.haibe.kains@utoronto.ca
Phone +14165818626
Organization name Princess Margaret Cancer Centre
Department Princess Margaret Research
Lab Bioinformatics and Computational Genomics
Street address 610 University Avenue
City Toronto
State/province Ontario
ZIP/Postal code M5G 2M9
Country Canada
 
Platform ID GPL8490
Series (2)
GSE20713 Epigenetic portraits of human breast cancers
GSE22281 Epigenetic portraits of human breast cancers (various cell lines methylation data)

Data table header descriptions
ID_REF
VALUE Average Beta values

Data table
ID_REF VALUE
cg00000292 0.8621591
cg00002426 0.9200878
cg00003994 0.04078076
cg00005847 0.3928755
cg00006414 0.03802395
cg00007981 0.0265289
cg00008493 0.9449293
cg00008713 0.03619419
cg00009407 0.01445021
cg00010193 0.452032
cg00011459 0.9246154
cg00012199 0.01654466
cg00012386 0.02837838
cg00012792 0.03101114
cg00013618 0.3920863
cg00014085 0.01958447
cg00014837 0.6241688
cg00015770 0.4057652
cg00016968 0.5378717
cg00019495 0.05650596

Total number of rows: 27578

Table truncated, full table size 577 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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