How to call variants and methylation across the human genome
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- Published on: December 4 2024
Explore Oxford Nanopore’s ultra-rich multiomic workflows for comprehensive human variation analysis.
Learning objectives
- 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
