Resource Centre
Publication 
Yaniv Erlich: A vision for Ubiquitous Sequencing
Publication 
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
Publication 
Whole genome sequencing for rapid characterization of rabies virus using nanopore technology
Publication 
Whole-genome nanopore sequencing and automatic downstream analysis of respiratory syncytial virus using RSVTyper
Publication 
Whole genome assembly of a hybrid Trypanosoma cruzi strain assembled with nanopore sequencing alone
Publication 
WGS of a cluster of MDR Shigella sonnei utilising Oxford Nanopore R10.4.1 long-read sequencing
Publication 
Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing
Publication 
Visualisation and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR
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Viral and bacterial profiles in endemic influenza A virus infected swine herds using nanopore metagenomic sequencing on tracheobronchial swabs
Publication 
Verkko2: integrating proximity ligation data with long-read De Bruijn graphs for efficient telomere-to-telomere genome assembly, phasing, and scaffold
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Validation of HPV genotyping by Oxford Nanopore sequencing in FFPE tissues and ThinPrep anal and gynaecological samples
Publication 
Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
Publication 
VACmap: an accurate long-read aligner for unravelling complex genomic rearrangements
Publication 
Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
Publication 
Utilising nanopore direct RNA sequencing of blood from patients with sepsis for discovery of co- and post-transcriptional disease biomarkers
Publication 
Using nanopore sequencing to identify bacterial infection in joint replacements: a preliminary study
Publication 
Using a mobile nanopore sequencing lab for end-to-end genomic surveillance of Plasmodium falciparum: a feasibility study
Publication 
Using long-read sequencing to detect imprinted DNA methylation
Publication 
Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
Publication 
Use of MinION to resolve repeats in B. pertussis clinical isolate genomes