Resource Centre
Video 
Core lab webinar series: A new 'gold standard' solution for complete plasmid sequencing
Publication 
Telomere-to-telomere phased genome assembly using error-corrected Simplex nanopore reads
Poster 
Targeted long-read sequencing for genetic diversity identification of the zoonotic Cryptosporidium sp.
Poster 
Squiggle analysis for metagenomic viability inference
Publication 
Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling
Publication 
Single-Cell Omics for Transcriptome CHaracterization (SCOTCH): isoform-level characterisation of gene expression through long-read single-cell RNA seq
Publication 
Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
Publication 
Resolving RH and GYP hybrid alleles while accessing the entire blood group genome with nanopore adaptive sampling
Publication 
Real time selective sequencing using nanopore technology
Poster 
Rapid genome surveillance of SARS-CoV-2 and portable DNA sequencing technology
Publication 
Prospective, multicentre validation of a platform for rapid molecular profiling of central nervous system tumours
Poster 
A POretable Metagenomics Pipeline (aPOMP): Fast and Efficient Nanopore sequencing-based metagenomics
Workflow 
Protocol overview: interaction-free whole-genome sequencing
Poster 
NCM 2022: Emu: microbiome profiling software for 16S rRNA Oxford Nanopore Technologies reads
Poster 
NCM 2022: Can nanopore long-read sequencing replace current cytogenetic methods in clinical genetic diagnostics?
Video 
NCM 2023 Houston: Enrichment strategies for recovery of Avian influenza virus from samples using MinION
Poster 
NanopoReaTA: a user-friendly tool for nanopore-seq real-time transcriptional analysis
Publication 
Nanopore adaptive sampling of a metagenomic sample derived from a human monkeypox case
Publication 
NANOME: a Nextflow pipeline for haplotype-aware allele-specific consensus DNA methylation detection by nanopore long-read sequencing
Publication 
Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases
