The mtDNA-control region targeted PCR product size is ~900 bp, it is A+T (Adenine & Thymine) rich region compared to other normal mtDNA regions/genes. While sequencing (sanger) this A+T rich sites are blocking and after I cant able to get further good sequences/signals. So anyone please tell me how to overcome this problem.   

More Kameshpandian Paramasivam's questions See All
Similar questions and discussions