Hi,

I used the M-values from 450k methylation data for analysis using limma workflow. How do I interpret the results? Does the fold change from the analysis mean hypo methylated vs hyper-methylated cpg sites versus the control? I know it means expression threshold if i am working with RNAseq, but since i am using a methylation dataset is the p-value the only vital information. My goal is to find differentially methylated regions but also identifying hypomethylated and hypermethylated cpg sites.