TOP
Sanger sequencing service
Why are the sequencing results not the sequence I need?
Why does the sequencing peak plot result in a decaying trend after 300-400bp?
Why must fragment lengths be filled in for PCR samples?
Why is the sequencing result positive when the synthesized primer information is filled in and reverse sequencing is told?
Why did the sequencing fill out the sequencing pass 3k and the sequencing result was only about 1k?