Clinical research
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Discover hidden variation in your samples
Oxford Nanopore sequencing delivers the most comprehensive insights into your clinical research samples — in one go. It enables real-time analysis of native DNA or RNA reads of any length (20 bp to >4 Mb), and combined with best-practice end-to-end workflows, facilitates complete characterisation of single nucleotide variants (SNVs), structural variants (SVs), repeats, phasing, transcript isoforms, and epigenetic modifications. Scalable and affordable, Oxford Nanopore sequencing offers researchers a cost-effective solution to the challenges faced by legacy sequencing platforms.
Featured content
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New approaches for human and clinical research
Discover how real-time, scalable Oxford Nanopore sequencing technology is being used to deliver novel, actionable insights across the clinical research field. Featured case studies show how the technology uncovers hidden genomic variation in rare and complex disease and its potential to end the diagnostic odyssey and transform leukaemia classification.
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24-hour human whole-genome sequencing
Oxford Nanopore human whole-genome sequencing enables faster-than-ever sample-to-answer turnaround times. Learn how through streamlined sample preparation, real-time, on-demand sequencing, and a simple data analysis workflow, it is possible to go from research sample to variant information in just 24 hours.
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Recommended device for clinical research
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PromethION 24
Combining up to 24 independently addressable, high-capacity flow cells with powerful, integrated compute, PromethION 24 delivers flexible, on-demand access to terabases of ultra-rich sequencing data — ideal for comprehensive variant identification across large numbers of clinical research samples.
