Upcoming Webinar June 22: Streamlining Variant Identification and Analysis

The path from DNA sequencing to variant interpretation can be long and complex and can require a mastery of many bioinformatics applications and online databases. Each additional step in the pipeline can affect the accuracy and completeness of the results. Looking for an easier way? To learn about integrated point-and-click workflows for assembly, variant calling, and variant annotation, join us for a free 1-hour webinar on Wednesday, June 22nd at 11:00 CDT. DNASTAR Senior Product Manager Matt Keyser will present a live demo showing how to:

• Perform sequence assembly and variant calling for Sanger, NGS or long-read data.
• Choose a downstream analysis method that best fits your research goals and data type.
• Identify significant variants through a powerful filtering tools and rich graphical views.
• Use links to instantly navigate to online database entries for variants and/or their related genes.

The webinar will be hosted by Senior Content Developer, Sharon Page.