Streamlining Variant Identification and Analysis Webinar

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? Watch this webinar presented by DNASTAR Senior Product Manager Matt Keyser to learn about integrated point-and-click workflows for assembly, variant calling, and variant annotation, including 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.