Resource Centre
Getting started guide )
Getting started guide: targeted sequencing
Video )
Adaptive sampling with Oxford Nanopore
Publication )
Clinical validation and utility of targeted nanopore sequencing for rapid pathogen diagnosis and precision therapy in lung cancer patients
Case study )
Case study: unlocking the abundance of information within environmental microbiomes
Case study )
Case study: from seed to harvest — protecting food crops with a single platform
Case study )
Case study: bringing genomics to the forefront of biodiversity conservation
White paper )
White paper: plant, animal, and environmental sequencing
Video )
AMP 2025: Long-range PCR meets long-read sequencing to resolve challenging ACMG tier 3 carrier screening genes
Publication )
RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease
Poster )
Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels
Publication )
Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles
Poster )
An end-to-end workflow for pharmacogenomic target enrichment, star allele annotation, and CYP2D6 resolution using nanopore sequencing
Workflow )
Workflow overview: microbial amplicon barcoding
Workflow )
Workflow overview: 16S sequencing
Publication )
Deep intronic SVA_E insertion identified as the most common pathogenic variant associated with Canavan disease: a diagnostic blind spot
Getting started guide )
Getting started guide: human genomics
Workflow )
Workflow overview: amplicon sequencing
Workflow )
Workflow overview: pharmacogenomics with adaptive sampling
Case study Case study: streamlining routine CRISPR validation with Oxford Nanopore sequencing
Workflow )
Workflow overview: mpox virus sequencing
