Resource Centre
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Long-read transcriptomics of a diverse human cohort reveals ancestry bias in gene annotation
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CRISPR-Cas9-induced double-strand breaks disrupt maintenance of epigenetic information
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Leveraging artificial intelligence community analytics and nanopore metagenomic surveillance to monitor early enteropathogen outbreaks
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Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
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Targeted sequencing and iterative assembly of near-complete genomes
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Single-cell long-read whole-genome sequencing reveals somatic transposon activity in human brain
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Reproducibility and accuracy of bacterial methylome profiling using Oxford Nanopore Technologies nanopore sequencing platform
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Application of FreezeTB, a targeted nanopore sequencing assay, for identification of drug resistance and lineages among pulmonary tuberculosis cases
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Transcriptional readthrough precedes alternative splicing programs triggered in CML cells by imatinib
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DNA methylation reprogramming in marsupial embryos is restricted to the extraembryonic lineage
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Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles
Publication ![Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders](https://a.storyblok.com/f/196663/94b60f6ad1/low-resolution-png-dna_wide_highres_1-16-1_1.png/m/700x470/filters:format(webp))
Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders
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Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing
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Whole-genome nanopore sequencing and automatic downstream analysis of respiratory syncytial virus using RSVTyper
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Nanopore direct RNA sequencing reveals METTL2A-mediated m3C sites in poly(A) RNA
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Pre-phasing long reads improves structural variant genotyping
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Enriching for answers in rare diseases
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Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision-making
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Novel multiplex family-wide PCR and nanopore sequencing of amplicons (FP-NSA) approach for surveillance of influenza- and coronaviruses
Publication Decoding the human PBMC isonome: isoform-level resolution with single-cell long-read transcriptomics
