Calling methylation in the human genome with PCR-free nanopore sequencing
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Overview
Methylation plays a fundamental role in regulating gene expression; aberrant methylation patterns are strongly associated with numerous diseases, such as cancer and developmental disorders. With PCR-free nanopore sequencing of native DNA, methylation can be directly detected at single-nucleotide resolution. This end-to-end workflow provides a simple solution for genome-wide methylation calling from a human blood research sample.
In this workflow, you will:
- Find out how PCR-free nanopore sequencing enhances methylation detection
- Discover our best practice sequencing workflow in detail, starting from the recommended extraction method, through to primary analysis
- Learn about our recommended sequencing kit and devices