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Publication
CRISPR-Cas9-induced double-strand breaks disrupt maintenance of epigenetic information
December 3 2025
Knowledge exchange
Fast answers and the most complete view: 24-hour whole-genome sequencing with Oxford Nanopore
November 25 2025
Publication
Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq
November 25 2025
Publication
Targeted sequencing and iterative assembly of near-complete genomes
November 24 2025
Publication
Single-cell long-read whole-genome sequencing reveals somatic transposon activity in human brain
November 20 2025
Webinar
Advancing rAAV Characterisation with Oxford Nanopore Sequencing
November 20 2025
Publication
Reproducibility and accuracy of bacterial methylome profiling using Oxford Nanopore Technologies nanopore sequencing platform
November 19 2025
Video
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
November 18 2025
Video
Sequencing the wild: unlocking animal and marine metagenomes with Oxford Nanopore
November 18 2025
Video
Revealing hidden genomic variation in Parkinson’s disease
November 18 2025
Publication
Application of FreezeTB, a targeted nanopore sequencing assay, for identification of drug resistance and lineages among pulmonary tuberculosis cases
November 17 2025
Publication
Transcriptional readthrough precedes alternative splicing programs triggered in CML cells by imatinib
November 14 2025
Brochure
Brochure: biopharma — cell and gene therapies
November 14 2025
Webinar
Transforming hereditary cancer sequencing with adaptive sampling target enrichment
November 11 2025
Poster
Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels
November 11 2025
Publication
DNA methylation reprogramming in marsupial embryos is restricted to the extraembryonic lineage
November 11 2025
Publication
Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles
November 10 2025
Video
cfDNA methylation sequencing: a precision tool for early detection of neurodegenerative disorders
November 5 2025
Publication
Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders
November 3 2025
Publication
Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing
November 3 2025

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About Oxford Nanopore

© 2008 - 2025 Oxford Nanopore Technologies plc. All rights reserved. Registered Office: Gosling Building, Edmund Halley Road, Oxford Science Park, OX4 4DQ, UK | Registered No. 05386273 | VAT No 336942382. Oxford Nanopore Technologies, the Wheel icon, EPI2ME, Flongle, GridION, Metrichor, MinION, MinIT, MinKNOW, Plongle, PromethION, SmidgION, Ubik and VolTRAX are registered trademarks of Oxford Nanopore Technologies plc in various countries. Oxford Nanopore Technologies products are not intended for use for health assessment or to diagnose, treat, mitigate, cure, or prevent any disease or condition.

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Resource Centre

CRISPR-Cas9-induced double-strand breaks disrupt maintenance of epigenetic information

Fast answers and the most complete view: 24-hour whole-genome sequencing with Oxford Nanopore

Transcriptome-wide profiling of alternative splicing regulators with CRISPore-seq

Targeted sequencing and iterative assembly of near-complete genomes

Single-cell long-read whole-genome sequencing reveals somatic transposon activity in human brain

Advancing rAAV Characterisation with Oxford Nanopore Sequencing

Reproducibility and accuracy of bacterial methylome profiling using Oxford Nanopore Technologies nanopore sequencing platform

Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing

Sequencing the wild: unlocking animal and marine metagenomes with Oxford Nanopore

Revealing hidden genomic variation in Parkinson’s disease

Application of FreezeTB, a targeted nanopore sequencing assay, for identification of drug resistance and lineages among pulmonary tuberculosis cases

Transcriptional readthrough precedes alternative splicing programs triggered in CML cells by imatinib

Brochure: biopharma — cell and gene therapies

Transforming hereditary cancer sequencing with adaptive sampling target enrichment

Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels

DNA methylation reprogramming in marsupial embryos is restricted to the extraembryonic lineage

Proof-of-principle: Nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles

cfDNA methylation sequencing: a precision tool for early detection of neurodegenerative disorders

Oxford Nanopore Technologies [ONT] sequencing: clinical validation in genetically heterogeneous disorders

Ensilication preserves high-molecular-weight native DNA for clinical long-read sequencing

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