Structural and epigenetic characterisation of D4Z4 arrays in FSHD using Oxford Nanopore multiomic sequencing
- shared.published_on: May 19 2026
Nanopore sequencing enables comprehensive resolution of D4Z4 repeat structure, haplotype, methylation, and chromatin accessibility, providing a consolidated approach to genetic and epigenetic characterisation of facioscapulohumeral muscular dystrophy (FSHD).
Download the poster to find out:
- How multiomic nanopore sequencing resolves FSHD
- About the methylation variation in D4Z4 haplotypes
- How ultra-long nanopore reads distinguish repeat lengths in all haplotypes
