Masterclass: How to call variants and methylation across the human genome | LC25
Explore Oxford Nanopore’s ultra-rich multiomic workflows for comprehensive human variation analysis — including SNVs, structural variants, methylation, STRs, CNVs, and phasing.
In this masterclass, you will learn:
How to obtain multiomic data from a single sequencing run
The sample-to-answer workflow: from PCR-free library prep to high-output sequencing and intuitive data analysis
Where to access additional online resources
