NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1072290 Query DataSets for GSM1072290
Status Public on Mar 08, 2013
Title 786-O_SAHA_NoE
Sample type genomic
 
Source name 786-O Cell Line
Organism Homo sapiens
Characteristics Sex: male
treatment: SAHA treated
cell line: 786-O Cell Line
Treatment protocol 2x10^5 nuclei were treated with 1x M.SssI buffer and 50U of M.SssI for 15 minutes. A no-enzyme control was included. SAHA treatment was performed for 24hours with 1uM SAHA
Growth protocol Cells were grown under standard conditions
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was extracted using standard phenol chloform procedures with ethanol precipitation. Zymo EZ DNA kit was used for bisulfite conversion
Label Cy5 and Cy3
Label protocol Standard Illumina labeling protocol
 
Hybridization protocol Bisulfite converted DNA was amplified, fragmented and hybridized to the Illumina 450k methylation array using standard Illumina protocols
Scan protocol Beadchips were imaged using Illumina BeadArray Reader using standard recommended Illumina scanner setting.
Description male, renal cancer cell line, SAHA treated
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.Data points were marked “NA” if 1) Probes contained 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 background subtracted.
 
Submission date Jan 29, 2013
Last update date Mar 08, 2013
Contact name Kurinji Pandiyan
Organization name University of Southern California
Department Department of Urology - Norris Comprehensive Cancer Center
Street address 1441 Eastlake Avenue NOR 7344
City Los Angeles
ZIP/Postal code 90033
Country USA
 
Platform ID GPL13534
Series (2)
GSE38858 AcceSssIble Assay to Study the Chomatin Accessibility and DNA Methylation
GSE43851 Functional DNA methylation is accompanied by chromatin accessibility [methylation]

Data table header descriptions
ID_REF
VALUE 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).

Data table
ID_REF VALUE
cg00000029 0.801714804
cg00000108 0.951492983
cg00000109 0.849616611
cg00000165 0.218220548
cg00000236 0.834358112
cg00000289 0.638675629
cg00000292 0.825792346
cg00000321 0.222552523
cg00000363 0.386033523
cg00000622 0.014070711
cg00000658 0.846414233
cg00000714 0.233712821
cg00000721 0.895274809
cg00000734 0.114375774
cg00000769 0.029326724
cg00000807 0.756470161
cg00000884 0.599183453
cg00000905 0.159973495
cg00000924 0.340961129
cg00000948 0.786415354

Total number of rows: 485577

Table truncated, full table size 10858 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap