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 )
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
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
Video )
Unlocking the banana pangenome: harnessing genetic diversity
Case study )
Case study: understanding the drivers of oncogenesis
Video )
Ultra-fast deep-learned classification algorithms for diagnosing pediatric CNS and solid tumors
Publication )
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
