Oxford Nanopore Technologies

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Oxford Nanopore Technologies is behind the world's only portable, real-time DNA / RNA sequencer, the MinION™. Scaling up to the PromethION™ and GridION™ syst...

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Accelerating precision oncology Real-time genomic and epigenomic profiling with Oxford Nanopore

Turning data into answers Rare disease case studies from clinical researchers

Full-length 16S sequencing in clinical research Swedish hospital evaluation

Continental-scale genomic surveillance of Plasmodium falciparum malaria

Implementación de la Secuenciación de Próxima Generación en el Laboratorio de Microbiología

From targeted sequencing to respiratory metagenomics transforming pathogen detection

Closing the gap in the clinical microbiology lab with next-generation sequencing

Advancing carrier screening and diagnostic applications research with long-read sequencing

Bacterial and fungal isolate sequencing with NO-MISS

Advancing mRNA therapeutics with sequencing

Genomics by Africans, for Africans” South Africa Prof Shahida Moose

Scaling Genomics in India From Local Access to National Impact Dr Rajesh Pandey

Genomics in the Middle East From Understudied to Closing the Gap Dr. Ahmad Abou Tayoun

The African Cancer Atlas Advancing Precision Oncology Through Genomic Diversity

Adaptive Sampling Webinar

The impact of rapid sequencing for healthcare systems Sebastian Brandner

Methylation Analysis Webinar

16S MAB Kit Webina

Consolidating assays to deliver faster results Rebecca Ellmers

Direct RNA Nanopore Explains

London Calling 2026 Rethink what's possible Register now

Nanopore sequencing for clinical research from critical care to complex genomic signatures

Unlocking rare diseases with nanopore sequencing

Native methylation sequencing for analysis of neurodegenerative conditions

A new era of biological discovery

Richer insights from Adaptive Sampling Targeted panels without the probes

The potential of a single platform for clinical assays Alona Sosinsky

Ask more of your sequencing

Investigating structural variants in undiagnosed genetic diseases

Revolutionising the future of rare neurological disease diagnosis