DNASTAR Senior Product Manager
Lasergene has long supported the assembly of raw sequence reads with simultaneous variant detection. But what if your starting point is a set of already-assembled sequences from related species or viral strains? MegAlign Pro now features a variant analysis workflow that can compute variants following a multiple sequence alignment. This workflow is ideal for many types of sequences, including viral, mitochondrial, and chloroplast genome sequences.
Whatever your starting point, learn the best method for finding variants in our 1-hour webinar, Comprehensive variant analysis: from raw sequence data to aligned genomes .
In this webinar, DNASTAR Product Manager Matthew Keyser demonstrates MegAlign Pro’s new variant analysis capabilities using example COVID and mitochondrial genome data sets. He also compares and contrasts this type of variant analysis with the type performed using SeqMan Ultra.
Watch this on-demand webinar to learn about the comprehensive variant analysis capabilities in Lasergene
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