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Comprehensive
“Most comprehensive and full-feature alignment software I have found.”
Following assembly, SeqMan Ultra uniquely offers you the ability to easily edit your assembled data – exposing or trimming ends, introducing mutations – as well as analyzing your assembled data, including viewing chromatograms, evaluating coverage, analyzing variants, and examining multiple samples organized within a single contig.
SeqMan Ultra accurately assembles Sanger ABI sequencing data with or without a reference, and includes an easy-to-use interface for previewing and trimming trace data.
GeneQuest
Finding and annotating the genes and regulatory elements on a sequence can often prove to be a challenge without a centralized tool for evaluating multiple analysis methods.
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