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 .” This free webinar will be presented by DNASTAR Product Manager Matt Keyser on Wednesday, December 7th at 11 am CST.
Matt will demonstrate MegAlign Pro’s new variant analysis capabilities using example COVID and mitochondrial genome data sets. He will also compare and contrast this type of variant analysis with the type performed using SeqMan Ultra, and take your questions.
Join us for our free variant analysis webinar on Wednesday, December 7th.
By registering for this webinar, you are giving consent for joining our email list for technical tips and special offers.
Unable to make the live webinar? No problem.
Please register anyway, and we will send you a link to the recorded webinar when it’s available.