Table 1.
Base conversion | |||||||
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Category | Endonuclease digestion | Affinity enrichment | Bisulfite-dependent | Bisulfite-free | |||
Methods | MRE-seq | MeDIP-seq | MBD-seq | RRBS | WGBS | TAPS | EM-seq |
Resolution | Single-base | 150–300 bp | Single-base | ||||
Coverage | – | +/– | + + | ||||
DNA input | + | + | + + | – | |||
Cost | – | – | + + | – | |||
Application | Site-specific studies | Low-resolution, large-scale studies | High resolution, whole-genome studies | ||||
Pros | Cost-effective, user-friendly | High sensitivity, low cost | Detect whole-genome methylation at single-base | ||||
Cons | Enzyme-dependent methylation detection; incomplete digestion | Low resolution; biased towards highly methylated regions | DNA degradation; high cost; reduced sequence complexity | Unsuitable for single cells; Large investment |
EM-seq = Enzymatic Methyl-seq, MBD = methyl-CpG-binding domain protein, MeDIP = methylated DNA immunoprecipitation, MRE = methylation sensitive restriction enzyme, RRBS = reduced representation bisulfite sequencing, -seq = sequencingg, TAPS = TET-assisted pyridine borane sequencing, WGBS = whole-genome bisulfite sequencin.
Coverage, DNA input and cost in table 1 are divided into 5 levels, followed by + + > + > +/– > – > – –.