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Sample GSM494389 Query DataSets for GSM494389
Status Public on May 12, 2010
Title MPCu, MeDIP, Rep 2
Sample type genomic
 
Channel 1
Source name MeDIP DNA, undifferentiated skeletal MPC
Organism Homo sapiens
Characteristics tissue: skeletal muscle
cell type: mesenchymal stem cells
differentiation: undifferentiated
medip antibody: 5-methyl cytosine antibody
Treatment protocol Genomic DNA was isolated, fragmented and used for MeDIP.
Growth protocol The muscle progenitors were cultured in Lonza commercial medium for up to 4-8 passages.
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was purified and fragmented by sonication to 300-500 bp fragments. 5-methylcytosine (5-mC)-enriched fragments were immunoprecipitated using anti-5mC antibodies (Diagenode). Precipitated and input DNA was amplified using the WGA2 kit (Sigma-Aldrich) and cleaned up.
Label Cy5
Label protocol Labeling done by NimbleGen as per normal service protocol. Input and MeDIP DNA were labeled with Cy3 and Cy5, respectively.
 
Channel 2
Source name Input DNA, undifferentiated skeletal MPC
Organism Homo sapiens
Characteristics tissue: skeletal muscle
cell type: mesenchymal stem cells
differentiation: undifferentiated
medip antibody: none
Treatment protocol Genomic DNA was isolated, fragmented, labeled and hybridized onto arrays.
Growth protocol The muscle progenitors were cultured in Lonza commerciall medium for up to 4-8 passages
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was purified and fragmented by sonication to 300-500 bp fragments. Precipitated and input DNA was amplified using the WGA2 kit (Sigma-Aldrich) and cleaned up.
Label Cy3
Label protocol Labeling done by NimbleGen as per normal service protocol. Input and MeDIP DNA were labeled with Cy3 and Cy5, respectively.
 
 
Hybridization protocol Hybridization done by NimbleGen as per normal service protocol. Labeled DNA was hybridized on promoter arrays.
Scan protocol Scanning done by NimbleGen as per normal service protocol.
Description MPCu_2_MeDIP
Data processing log2 (MeDIP/Input) with biweight mean of values subtracted.
 
Submission date Jan 07, 2010
Last update date May 12, 2010
Contact name Philippe Collas
Organization name University of Oslo
Department Institute of Basic Medical Sciences
Street address PO Box 1112 Blindern
City Oslo
ZIP/Postal code 0317
Country Norway
 
Platform ID GPL7408
Series (2)
GSE19794 DNA methylation in progenitor cells: MeDIP study
GSE19795 DNA methylation in progenitor cells

Data table header descriptions
ID_REF
VALUE log2(Cy5/Cy3) – biweight_mean

Data table
ID_REF VALUE
CHR01P000056753 -1.33
CHR01P000056853 -1.46
CHR01P000056953 -2.22
CHR01P000057053 -1.67
CHR01P000057153 -1.06
CHR01P000057253 -0.67
CHR01P000057353 -0.46
CHR01P000057453 -0.22
CHR01P000057553 0.44
CHR01P000057753 0.48
CHR01P000057853 -0.02
CHR01P000057953 0.65
CHR01P000058053 1.55
CHR01P000058153 1.58
CHR01P000058253 -0.58
CHR01P000058353 -0.61
CHR01P000058556 -0.66
CHR01P000058656 -0.49
CHR01P000058756 -0.37
CHR01P000058956 0.78

Total number of rows: 386230

Table truncated, full table size 8093 Kbytes.




Supplementary file Size Download File type/resource
GSM494389_MPCu_2_532.pair.gz 7.1 Mb (ftp)(http) PAIR
GSM494389_MPCu_2_635.pair.gz 7.0 Mb (ftp)(http) PAIR
Processed data included within Sample table

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