Resource Centre
Case study )
Case study: high-quality bacterial genome without the complexity
Publication )
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision-making
Publication )
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic
Poster )
Resolving challenging medically-relevant genes using nanopore sequencing
Poster )
Comprehensive resolution of challenging genomic variation with Oxford Nanopore telomere-to-telomere assemblies
Brochure )
Flyer: Oxford Nanopore 24-hour whole-genome sequencing for paediatric rare disease research
Workflow )
Protocol overview: interaction-free whole-genome sequencing
Publication )
Long-read whole-genome sequencing-based discovery of structural variants and their role in aetiology of non-syndromic ASD in India
Workflow Workflow overview: pharmacogenomics with adaptive sampling
Publication )
The Platinum Pedigree: a long-read benchmark for genetic variants
Workflow )
Workflow overview: large cohort sequencing
Workflow )
Workflow overview: tumour-normal sequencing
Poster )
Multiomics whole-genome characterisation of a cancer genome using Oxford Nanopore sequencing
Brochure )
Flyer: pharmacogenomics with Twist
Workflow )
Workflow overview: human variant calling
Brochure )
Flyer: methylation detection
Publication )
ClairS-TO: a deep-learning method for long-read tumour-only somatic small variant calling
Publication )
Targeted long-read sequencing as a single assay improves diagnosis of spastic-ataxia disorders
Getting started guide )
Getting started guide: single-cell transcriptomics
Publication )
Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes
