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
Video )
Nanopore sequencing: insights from neonatal intensive care to cancer
Video )
Human genome sequencing on PromethION webinar
Video )
Core lab webinar series: New dimensions of biology revealed by full-length sequencing of single-cell and spatial assays
Publication )
Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
Video )
Virtual Nanopore Day, Australia: Bioinformatics
Video )
Virtual Nanopore Day, LA
Video )
Virtual Nanopore Day, Australia. Cancer research with nanopore sequencing
Video )
Cancer WGS on the PromethION
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 )
Using Oxford Nanopore sequencing in grapevine breeding
Publication )
Using long-read sequencing to detect imprinted DNA methylation
