Performance of Oxford Nanopore whole-genome methylation sequencing in human genetics applications
- shared.published_on: May 19 2026
Genomic DNA can be sequenced on Oxford Nanopore devices without the need for fragmentation, amplification, or strand synthesis, improving mappability and retaining long-range data for methylation phasing.
Download the poster to discover:
- How benchmarking of nanopore methylation analysis reveals lower bias, higher mapping rates, greater reproducibility, and faster analysis than seen with bisulfite data
- How a paternally inherited partial deletion of SNURF imprinting control region disrupts imprinting across Prader-Willi locus (15q11.2) in research samples from a family affected by Prader-Willi syndrome
