Resource Centre
Bioinformatics tool )
Yanocomp: robust prediction of m6A modifications in individual nanopore direct RNA reads
Workflow )
Workflow overview: tumour-normal sequencing
Workflow )
Workflow overview: 24-hour human whole-genome sequencing
Workflow )
Workflow overview: plant genome assembly
Workflow )
Workflow overview: large cohort sequencing
Workflow )
Workflow overview: human variant calling
Workflow )
Workflow overview: direct RNA sequencing
Poster )
Whole genome Nanopore DNA analysis shows that chronic corticosterone supplementation results in altered sperm DNA methylation.
Video )
Whole-genome insights: nanopore sequencing in neuropathology
Learning )
Which library prep workflow is right for my experiment?
Video )
Resolving complex genomic structures and regulation patterns in cervical cancer
Video )
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
Video )
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
Company news )
"...we need a better name than follow through"
Company news )
"...a wafer thin update"
Knowledge exchange )
Directly detect and phase genomic methylation with high reproducibility and low bias
Publication )
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
Video )
Using Oxford Nanopore sequencing in grapevine breeding
Publication )
Using long-read sequencing to detect imprinted DNA methylation
Poster )
Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
