Resource Centre
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Unlocking rare diseases with nanopore sequencing
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Native methylation sequencing for analysis of neurodegenerative conditions
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Nanopore sequencing for clinical research: from critical care to complex genomic signatures
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Richer insights with Adaptive Sampling: targeted panels without probes for cancer predisposition, tumor profiling, and beyond
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Translational and clinical research applications of long-read sequencing technologies in oncology
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AGBT 2026: a new era of biological discovery
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Adaptive sampling with Oxford Nanopore
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AMP 2025: Rapid comprehensive molecular profiling of CNS tumors
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AMP 2025: Oxford Nanopore-based structural and epigenetic profiling of D4Z4 arrays in FSHD
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AMP 2025: Long-range PCR meets long-read sequencing to resolve challenging ACMG tier 3 carrier screening genes
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AMP 2025: Epigenomic diagnosis and prognosis of Acute Myeloid Leukemia
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Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
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Sequencing the wild: unlocking animal and marine metagenomes with Oxford Nanopore
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Revealing hidden genomic variation in Parkinson’s disease
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cfDNA methylation sequencing: a precision tool for early detection of neurodegenerative disorders
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How to sequence full-length 16S and ITS amplicons
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Sequencing from large scale to single cell — the new era of biological discovery
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Enhanced hereditary cancer screening through scalable parent-of-origin-aware genomic analysis
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Webinar: Microbes in microgravity: identifying diversity and adaptions
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Foodborne pathogen surveillance with Oxford Nanopore sequencing