Applied Long-Read Sequencing: Practical Workflows for Modern Genomic Research

Wednesday, January 28th at 11 am CDT

Are you getting the most out of your long-read sequencing data?

With advances in PacBio and Oxford Nanopore technologies, researchers are generating more long-read data than ever, yet many still struggle to convert those reads into high-quality assemblies and actionable insights. Lasergene provides optimized workflows purpose-built for long-read applications, supporting de novo and reference-guided assembly with variant calling, as well as metagenomic, RNA-seq, ChIP-seq, and miRNA analyses.

In this session, DNASTAR's Matt Keyser will demonstrate how to:

• Generate high-quality assemblies from long-read datasets
  
  
• Visualize, filter, and interpret results with intuitive analysis tools
  
  
• Apply long-read workflows to real datasets across multiple research areas
  
  
• Incorporate phased data analysis into downstream interpretation

Matt will wrap up the software demo with a live Q&A. All registrants will also receive a link to the webinar recording after the live event.