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Sample GSM788251 Query DataSets for GSM788251
Status Public on Apr 19, 2012
Title Control NOK expressing EGFP
Sample type genomic
 
Channel 1
Source name IP_NOKG
Organism Homo sapiens
Characteristics cell type: NOK
retrovirus expression: EGFP (control gene)
treatment: methylated enriched
Treatment protocol Retroviral Transduction with EGFP
Extracted molecule genomic DNA
Extraction protocol Genomic DNA (gDNA) were extracted from 1 million cells by standard phenol:chloroform method. gDNA were then fragmented by MseI digestion (37°C, 16h) prior to enrichment for CpG-methylated DNA using a MBD2b/MBD3L1-conjugated magnetic bead-based system according to manufacturer’s protocol (MethylCollector Ultra kit, #55005, Active Motif Europe, Belgium).
Label Cy5
Label protocol Briefly the DNA is labelled by klenow extension using Cy3- (Input) or Cy5-(MeDIP) labelled random primers.
 
Channel 2
Source name T_NOKG
Organism Homo sapiens
Characteristics cell type: NOK
retrovirus expression: EGFP (control gene)
treatment: non-enriched
Treatment protocol Retroviral Transduction with EGFP
Extracted molecule genomic DNA
Extraction protocol Genomic DNA (gDNA) were extracted from 1 million cells by standard phenol:chloroform method. gDNA were then fragmented by MseI digestion (37°C, 16h) prior to enrichment for CpG-methylated DNA using a MBD2b/MBD3L1-conjugated magnetic bead-based system according to manufacturer’s protocol (MethylCollector Ultra kit, #55005, Active Motif Europe, Belgium).
Label Cy3
Label protocol Briefly the DNA is labelled by klenow extension using Cy3- (Input) or Cy5-(MeDIP) labelled random primers.
 
 
Hybridization protocol Equal amounts (15ug) of labelled MeDIP and Input DNA are loaded onto the arrays and co-hybridized at 42 C for 16-20 hours.
Scan protocol The arrays are then washed, dryed on the NimbleGen dryer and scanned on the NimbleGen MS200 scanner.
Description 100718_HG18_CpG_Refseq_Prom_MeDIP
Data processing Data are extracted and analysed using the NimbleGen NimbleScan software (v2.6 in your case) using the default settings.
 
Submission date Aug 30, 2011
Last update date Apr 19, 2012
Contact name Muy-Teck Teh
E-mail(s) m.t.teh@qmul.ac.uk
Phone +442078827140
Organization name Queen Mary University of London
Department Centre for Clinical & Diagnostic Oral Sciences
Lab Head & Neck Cancer Unit
Street address Blizard Building, 4, Newark Street,
City London
State/province England
ZIP/Postal code E1 2AT
Country United Kingdom
 
Platform ID GPL14361
Series (1)
GSE31767 FOXM1 Orchestrates a Global Methylation Signature that Mimics the Cancer Epigenome

Data table header descriptions
ID_REF
VALUE log2 transformed methylation/input

Data table
ID_REF VALUE
1 -0.67
2 -0.48
3 0.01
4 0.08
5 -0.04
6 -0.05
7 0.81
8 1.09
9 -0.23
10 0.07
11 0.52
12 -0.62
13 -0.3
14 0.63
15 -0.31
16 -0.15
17 -0.54
18 -0.8
19 0.31
20 0.11

Total number of rows: 711794

Table truncated, full table size 8494 Kbytes.




Supplementary file Size Download File type/resource
GSM788251_60821202_532.pair.gz 11.6 Mb (ftp)(http) PAIR
GSM788251_60821202_635.pair.gz 11.5 Mb (ftp)(http) PAIR
GSM788251_60821202_ratio.gff.gz 9.8 Mb (ftp)(http) GFF
GSM788251_60821202_ratio_peak_pvalues.gff.gz 10.4 Mb (ftp)(http) GFF
GSM788251_60821202_ratio_peaks.gff.gz 91.4 Kb (ftp)(http) GFF
GSM788251_60821202_ratio_peaks_mapToFeatures_All_Peaks.txt.gz 446.7 Kb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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