Resource Centre
Publication )
ZCWPW1 loss-of-function variants in Alzheimer’s Disease
Workflow )
Workflow overview: pharmacogenomics with adaptive sampling
Workflow )
Workflow overview: human variant calling
Video )
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
Publication )
Verkko2: integrating proximity ligation data with long-read De Bruijn graphs for efficient telomere-to-telomere genome assembly, phasing, and scaffold
Video )
Variant segregation in rare disease singletons and duos using nanopore adaptive sampling
Video )
Variant phasing for antisense oligonucleotide design using adaptive sampling
Publication )
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
Video )
Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
Video )
Using Targeted Nanopore Technologies
Video )
Using Oxford Nanopore sequencing in grapevine breeding
Poster )
Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
Video )
Unlocking the banana pangenome: harnessing genetic diversity
Poster )
Unlocking the power of haplotype-based molecular breeding using long read DNA sequencing
Case study )
Case study: understanding the drivers of oncogenesis
Publication )
Ultrarapid and high-resolution HLA class I typing using transposase-based nanopore sequencing applied in pharmacogenetic testing
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 )
The utility of long-read sequencing in diagnosing early-onset Parkinson's disease
