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
Video )
William Jeck: Nanopore sequencing and rapid fusion testing – a ‘killer app’ in molecular pathology
Publication )
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
Publication )
Whole-genome sequencing of rare disease patients in a national healthcare system
Publication )
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
Poster )
Whole-genome sequencing in disease samples with haplotype resolved and annotated genetic variation
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
Events )
Webinar: Structural variants in the French-Canadian population
Video )
Webinar - Nanopore from 100 to 1000 genomes: towards a better understanding of phenotypes
Bioinformatics tool )
Vulcan: Improved long-read mapping and structural variant calling via dual-mode alignment
Publication )
Virus-derived variation in diverse human genomes
Events )
Virtual Nanopore Day, Australia - Rare Disease and Neurology
Video )
Virtual Nanopore Day, Edinburgh
Video )
Cloud computing for clinical nanopore fusion detection
Publication )
Variants at the ASIP locus contribute to coat color darkening in Nellore cattle
Publication )
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
