October 14, 2016 at 12:00 pm EDT
With our latest release, you can use Lasergene Genomics Suite to validate your NGS assemblies with Sanger data. Whether you are working with clinical sequencing data and need to confirm your variant calls, or want to validate synthetic DNA fragments or virtual clones, our new workflow makes it easier than ever to assemble all your read data together, and visualize Sanger and NGS results in a single project! See how it's done in our live demo, and have your questions answered by our NGS expert, Matthew Keyser.