Resource Centre
Publication )
Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
Video Revealing hidden genomic variation in Parkinson’s disease
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/filters:format(webp))
Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders
Publication )
Pre-phasing long reads improves structural variant genotyping
Publication )
Long-read genome sequencing and multi-omics in ageing and neurodegeneration
Poster )
Comprehensive resolution of challenging genomic variation with Oxford Nanopore telomere-to-telomere assemblies
Publication )
Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling
Case study )
Testimonial: Yaw Bediako
Publication )
Integrating long-read nanopore sequencing for precision resolution of genomic variants in dystonia
Publication )
Enhancing CYP2D6 genotyping with nanopore sequencing to address allele diversity P. vivax malaria elimination
Workflow )
Workflow overview: 24-hour human whole-genome sequencing
Getting started guide )
Getting started guide: human genomics
Application note Application note: Comprehensive genomic and epigenomic profiling with the Oxford Nanopore Hereditary Cancer Panel
Workflow )
Protocol overview: interaction-free whole-genome sequencing
Publication )
Identification of non-coding causative variant underlying Warsaw Breakage syndrome using long-read based genomic sequencing and transcriptome analysis
Publication )
Long-read single-cell genome, transcriptome and open chromatin profiling links genotype to phenotypes
Publication )
Long-read genomic and epigenomic profiling enhances timely comprehensive variant discovery in hypotonia and muscle weakness
Brochure Flyer: Hereditary Cancer Panel
Case study Case study: Oxford Nanopore sequencing at large cohort scale — new insights from the NIHR BioResource
Case study )
Case study: is the end to the diagnostic odyssey within reach?
