NCM 2022: How to generate assemblies and call variants

Summary:
Discover the approaches available for assembling your nanopore sequencing data and calling variants, including SNVs and structural variants.
Learning objectives:
Take your data analysis skills to the next level with this masterclass, where you will learn:

  • How to generate high-quality assemblies with nanopore sequencing data, including small and large genome assembly and metagenomic assembly approaches
  • All about analysis workflows for calling variants – including structural variants and SNVs
  • How to perform transcriptomic analysis, including at the single-cell level
Authors: Matt Attreed