Resource Centre

Quick and simple analysis of PCR products with nanopore reads

Native telomere sequencing of individual chromosomes using 3’ end adapter ligation with Telo-seq

Full CYP2D6 and pharmacogene resolution with Oxford Nanopore long reads

Automated single-platform telomere-to-telomere de novo genome assembly for human, plant, and animal genomes

Comprehensive genetic analysis of facioscapulohumeral muscular dystrophy by nanopore long-read whole-genome sequencing

• Human genomics
• Methylation
• Clinical research
• Variant calling

A new method using rapid nanopore metagenomic cell-free DNA sequencing to diagnose bloodstream infections: a prospective observational study

• Clinical research
• Infectious disease
• Microbiology
• Metagenomics

Nanomotif: identification and exploitation of DNA methylation motifs in metagenomes using Oxford Nanopore sequencing

• Methylation
• Bioinformatics
• Metagenomics

NanoImprint: a DNA methylation tool for clinical interpretation and diagnosis of common imprinting disorders using nanopore long-read sequencing

• Methylation
• Human genomics
• Bioinformatics
• PromethION

Single-Cell Omics for Transcriptome CHaracterization (SCOTCH): isoform-level characterisation of gene expression through long-read single-cell RNA seq

• Single cell
• Bioinformatics
• Transcriptomics

Nanopore sequencing-based episignature detection

• Methylation
• Human genomics
• Clinical research
• Whole genome

Multi-omics analysis reveals COVID-19 vaccine induced attenuation of inflammatory responses during breakthrough disease

• Transcriptome
• cDNA
• PromethION
• Human genomics
• Infectious disease

Long-read sequencing and structural variant characterisation in 1,019 samples from the 1000 Genomes Project

• Structural variation
• Human genomics
• Population genomics
• PromethION

Aneuploidy detection in pooled polar bodies using rapid nanopore sequencing

• Human genomics
• Reproductive medicine
• DNA

Profiling age and body fluid DNA methylation markers using nanopore adaptive sampling

• Methylation
• Human genomics
• Targeted
• MinION

Evaluation of NGS DNA barcoding for biosecurity diagnostic applications: case study from banana freckle incursion in Australia

• Microbiology
• Fungi
• MinION
• Real-time
• Portable

Stability of mosaic divergent repeat interruptions in X-linked dystonia-parkinsonism

• Human genomics
• Structural variation
• GridION
• Targeted

Single-molecule epitranscriptomic analysis of full-length HIV-1 RNAs reveals functional roles of site-specific m6As

• Microbiology
• Virus
• Transcriptomics
• RNA
• MinION

Human telomere length is chromosome end–specific and conserved across individuals

• Human genomics
• MinION
• Targeted
• Structural variation
• Long-read

Whole genome assembly of a hybrid Trypanosoma cruzi strain assembled with nanopore sequencing alone

• Microbiology
• Assembly
• Whole genome
• MinION

Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases

• Human genomics
• Clinical research
• Long-read
• Structural variation
• PromethION