Applied Long-Read Sequencing: Practical Workflows for Modern Genomic Research
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.
To learn more, watch this on-demand webinar to see DNASTAR’s Matt Keyser 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 wraps up the software demo with a live Q&A.
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