Entering edit mode
9.6 years ago
Saad Khan
▴
440
Do you have control/treatment data for both?
My suggestion would be to focus on promoter regions +/- 1kbp around TSS and quantify the methylation in each case, %methylation for BS-seq and counts per million for MeDIP-seq, then you can analyse differences with statistical test, merge datasets on gene accession number and perform correlation analysis.
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