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Structural and epigenetic characterisation of D4Z4 arrays in FSHD using Oxford Nanopore multiomic sequencing

Oxford Nanopore long reads
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  • Published on: May 19 2026
Poster on D4Z4 array characterisation in FSHD, featuring sequencing data, charts, and a DNA visual by Oxford Nanopore Technologies.

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
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