This exclusive and convenient service includes all steps necessary to determine the complete sequence of (large) DNA fragments. Simply submit your samples and a reference sequence and leave the work to BaseClear. We design and synthesize all primers necessary. If a reference sequence is not available, or if a clone contains an unknown insert, we sequence the DNA by using a primer walking strategy. We assemble the sequence data and compare these to the reference sequence (if available).
Fill in our Sanger sequencing survey, and win a Samsung tablet! Visit http://s.surveys.baseclear.com/sanger-sequencing. Closing date May 25, 2018.