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Comprehensive resolution of challenging genomic variants with Oxford Nanopore de novo genome assemblies

  • Published on: May 19 2026
Poster detailing genomic variant resolution using Oxford Nanopore de novo genome assemblies, featuring charts and diagrams.

Telomere-to-telomere (T2T) genome assemblies generated using long and ultra-long reads, combined with Pore-C, provide the most complete picture of the human genome for platinum-standard reference and complex variant analysis.

Download the poster to find out:

  • How to assemble T2T genomes using nanopore-only data
  • About characterising complex chromosomal translocations
  • How T2T assemblies can fully resolve haplotypes and previously unresolved structural variants (SVs)

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