Resource Centre
Workflow 
Workflow overview: tumour-normal sequencing
Workflow 
Workflow overview: 24-hour human whole-genome sequencing
Workflow 
Workflow overview: large cohort sequencing
Workflow 
Workflow overview: human variant calling
Publication 
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
Video 
Whole-genome insights: nanopore sequencing in neuropathology
Poster 
Whole-genome DNA sequencing using nanopore R10.4 promises best practice for single-cell variation detection and methylation profiling
Bioinformatics tool 
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment
Publication 
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
Publication 
VACmap: an accurate long-read aligner for unravelling complex genomic rearrangements
Video 
Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
Video 
Using nanopore sequencing: from first principles to applications
Poster 
Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing
Poster 
Understanding genetic variation in cancer using targeted long-read sequencing
Case study 
Case study: understanding the drivers of oncogenesis
Video 
Ultra-rich human data — variant analysis with EPI2ME
Publication 
Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
Video 
Transforming cancer care: redefining cancer characterization and predisposition insights through nanopore sequencing
Publication 
Third-generation single-molecule sequencing for preimplantation genetic testing of aneuploidy and segmental imbalances
Publication 
The utility of long-read sequencing in diagnosing early-onset Parkinson's disease
