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
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. Read case studies on rare and complex diseases and leukaemia classification.
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.
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.
