Masterclass: How to call variants and methylation across the human genome | LC25
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- Published on: May 19 2025
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
