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: large cohort sequencing
Workflow 
Workflow overview: human variant calling
Workflow 
Workflow overview: direct RNA sequencing
Video 
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
Video 
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
Knowledge exchange 
Directly detect and phase genomic methylation with high reproducibility and low bias
Webinar 
Uncovering hidden variation in rare and complex diseases webinar
Publication Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
Video 
Translational and clinical research applications of long-read sequencing technologies in oncology
Bioinformatics tool 
Towards inferring nanopore sequencing ionic currents from nucleotide chemical structures
Case study 
Testimonial: Jonathan Mill
Bioinformatics tool 
Targeted nanopore sequencing by real-time mapping of raw electrical signal with UNCALLED
Bioinformatics tool 
Systematic benchmarking of tools for CpG methylation detection from Nanopore sequencing
Video 
Structural variant analysis with Oxford Nanopore
Case study 
Case study: simple, simultaneous detection of epigenetic and genetic variants for insights into disease mechanisms
Publication 
The SEQC2 epigenomics quality control (EpiQC) study
Bioinformatics tool 
PycoMeth: A toolbox for differential methylation testing from nanopore methylation calls
