Resource Centre
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Yaniv Erlich: A vision for Ubiquitous Sequencing
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The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
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Whole genome sequencing for rapid characterization of rabies virus using nanopore technology
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Whole-genome nanopore sequencing and automatic downstream analysis of respiratory syncytial virus using RSVTyper
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Whole-genome long-read sequencing for rapid comprehensive molecular diagnostics of brain tumours
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Whole genome assembly of a hybrid Trypanosoma cruzi strain assembled with nanopore sequencing alone
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WGS of a cluster of MDR Shigella sonnei utilising Oxford Nanopore R10.4.1 long-read sequencing
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Wakhan: reconstruction of chromosome-scale copy number profiles of tumour genomes with long-read sequencing
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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
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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
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Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis
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VACmap: an accurate long-read aligner for unravelling complex genomic rearrangements
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Utilizing nanopore sequencing technology for the rapid and comprehensive characterization of eleven HLA loci
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Utilising nanopore direct RNA sequencing of blood from patients with sepsis for discovery of co- and post-transcriptional disease biomarkers
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Using nanopore sequencing to identify bacterial infection in joint replacements: a preliminary study
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Using a mobile nanopore sequencing lab for end-to-end genomic surveillance of Plasmodium falciparum: a feasibility study
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Using long-read sequencing to detect imprinted DNA methylation
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Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
