Choosing the best assembly strategy for your genomic sequencing data

Do you have whole genome NGS or long read sequencing data, but aren’t sure where to begin with assembly and analysis? Have you tried different assembly programs without satisfactory results? If so, this webinar is for you!

Join us on August 5 for an in-depth look at different assembly strategies for genomic sequencing data. DNASTAR Senior Product Manager, Matthew Keyser, will help you determine when to use different reference-based and de novo approaches, and how to perform a variety of polishing and correction techniques to close your genome. After assembly, see how to close gaps and prepare your genome sequence for annotation and downstream analysis.

This webinar will include discussion, Q&A, and a live software demo of the newest assembly and downstream analysis tools in Lasergene 17.1.

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