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Supported workflows include performing multiple and pairwise sequence alignments, phylogenetic analysis, assembling contigs of Sanger sequences, creating virtual clones, designing primers, and more.

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and provides extensive post-assembly analysis tools for both Sanger and NGS assemblies. When compared to the competition, our algorithm does the best job assembling Sanger sequences into a single contig, and calling the most accurate consensus sequence based on trace quality and shape.

Now you can reach your analysis goals more quickly with insightful features like batch editing, automated sequence annotation, access to a meticulously annotated plasmid vector map catalog, and full integration with NCBI databases.
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