Resource Centre
Getting started guide )
Getting started guide: microbial sequencing
Case study )
Case study: high-quality bacterial genome without the complexity
Workflow )
Workflow overview: Hereditary Cancer Panel
Publication )
Twist-ONT: combining nanopore sequencing with the Twist comprehensive viral research panel
Publication )
CRISPR-Cas9-induced double-strand breaks disrupt maintenance of epigenetic information
Publication )
Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing
Brochure )
Flyer: Oxford Nanopore 24-hour whole-genome sequencing for paediatric rare disease research
Application note )
Application note: Comprehensive genomic and epigenomic profiling with the Oxford Nanopore Hereditary Cancer Panel
Workflow )
Workflow overview: amplicon sequencing
Brochure Flyer: Hereditary Cancer Panel
Case study Case study: is the end to the diagnostic odyssey within reach?
Case study )
Case study: expanding reference genomes with T2T assembly to reflect global diversity
Case study )
Case study: exploring the future of rapid leukaemia diagnosis with a single-platform workflow
Workflow Workflow overview: pharmacogenomics with adaptive sampling
Publication )
A founder BRCA1 exonic duplication involving breakpoint in T2T reference genome-specific region results in constitutional fusion transcript
Case study Case study: streamlining routine CRISPR validation with Oxford Nanopore sequencing
Application note )
Application note: Oxford Nanopore whole-genome sequencing of foodborne pathogens
Workflow Protocol overview: direct-from-colony microbial sequencing (rapid Salmonella serotyping)
Workflow )
Workflow overview: mpox virus sequencing
Publication Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanisms
