Resource Centre
Video 
AGBT 2026: a new era of biological discovery
Getting started guide 
Getting started guide: targeted sequencing
Publication 
Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
Publication 
Feasibility of long-read nanopore sequencing for methylation-based classification of posterior fossa ependymomas
Workflow Workflow overview: Hereditary Cancer Panel
Publication 
Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
Video 
AMP 2025: Rapid comprehensive molecular profiling of CNS tumors
Video 
AMP 2025: Oxford Nanopore-based structural and epigenetic profiling of D4Z4 arrays in FSHD
Video 
AMP 2025: Long-range PCR meets long-read sequencing to resolve challenging ACMG tier 3 carrier screening genes
Video 
AMP 2025: Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia
Publication 
RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease
Knowledge exchange 
Fast answers and the most complete view: 24-hour whole-genome sequencing with Oxford Nanopore
Webinar 
Transforming hereditary cancer sequencing with adaptive sampling target enrichment
Publication 
Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles
Video 
cfDNA methylation sequencing: a precision tool for early detection of neurodegenerative disorders
Publication ![Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders](https://a.storyblok.com/f/196663/94b60f6ad1/low-resolution-png-dna_wide_highres_1-16-1_1.png/m/700x470)
Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders
Publication 
Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing
Video 
Sequencing from large scale to single cell — the new era of biological discovery
Video 
Enhanced hereditary cancer screening through scalable parent-of-origin-aware genomic analysis
Poster Resolving challenging medically-relevant genes using nanopore sequencing