SeqMan Ultra

SeqMan Ultra is a modern, intuitive sequence assembly application built on the foundation of our classic SeqMan Pro. SeqMan Ultra uses the most accurate algorithm available for Sanger sequence assemblies and provides extensive post-assembly analysis tools for both Sanger and NGS assemblies. When compared to the competition, our algorithm does the best job at assembling Sanger sequences into a single contig and calling the most accurate consensus sequence based on trace quality and shape.

SeqMan Ultra supports multi-sample Sanger assembly and gives you the flexibility to choose between a classic SeqMan Pro-style workflow or a genomics-driven approach.

Assemble multi-sample Sanger data directly in SeqMan Ultra using the classic SeqMan Pro algorithm and a user interface similar to that in SeqMan Pro. Or run multi-sample assemblies with SeqMan NGen to align Sanger data to human chromosomes and access advanced variant analysis tools like the Variant Annotation Database (available to Lasergene Genomics customers).

Following assembly, SeqMan Ultra uniquely offers you the ability to easily edit your assembled data—exposing or trimming ends, introducing mutations—as well as analyze your assembled results through chromatogram viewing, coverage evaluation, variant analysis, and multi-sample comparison within a single contig. With SeqMan Ultra, you can move seamlessly between classic Sanger workflows and advanced genomics-scale assemblies—all within a single, intuitive platform designed to deliver accuracy, flexibility, and control.