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
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
Bioinformatics tool )
PycoMeth: A toolbox for differential methylation testing from nanopore methylation calls
Video )
Profiling age and body fluid DNA methylation markers
Poster )
Poster: structural and epigenetic profiling of D4Z4 arrays in FSHD using Oxford Nanopore sequencing
