How does the preferences between these two methods play a role in genetic polymophism test? Can we choose one over the other? What are the circumstances that we use both?
DNA sequencing is preferable, it is more accurate for mutation detection, than RFLP especially if the SNP have not specific Restriction site. However, it is costly than RFLP. RFLP only reveal SNP. SO., the other types of mutations are only detectable by squencing