Resource Centre
Workflow )
Workflow overview: tumour-normal sequencing
Workflow )
Workflow overview: single-cell transcriptomics
Workflow )
Workflow overview: 24-hour human whole-genome sequencing
Workflow )
Workflow overview: plant genome assembly
Workflow )
Workflow overview: human variant calling
Video )
Whole-genome insights: nanopore sequencing in neuropathology
Learning )
Which library prep workflow is right for my experiment?
Knowledge exchange )
Turning data into answers: Rare disease case studies from clinical researchers
Video )
Nanopore sequencing: insights from neonatal intensive care to cancer
Video )
Democratising Genomic Diagnostics: A New Model for Global Childhood Cancer Care
Publication )
Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
Bioinformatics tool )
Verkko: telomere-to-telomere assembly of diploid chromosomes
Video )
Variant phasing for antisense oligonucleotide design using adaptive sampling
Publication )
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
Video )
Utilizing nanopore long-read sequencing to simplify hereditary movement disorder diagnostics
Video )
Utility of long-read whole-genome sequencing across diverse clinical genomic investigations: a single- center experience | LC26
Video )
Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
Video )
Using Oxford Nanopore sequencing in grapevine breeding
Video )
Using long-read sequencing for translational health research
Publication )
Using long-read sequencing to detect imprinted DNA methylation
