SeqMan II enables you to assemble fragment data from sequencing projects of any size - from a few fragments to tens of thousands of fragments - at the push of a button. SeqMan II removes unreliable data, including poor quality ends, sub-minimal length reads, and vector and contaminating host sequences in a single pass, then assembles the trimmed data and calls the consensus.
What's new in this version:
Primer WalkingSNP Discovery
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