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Scalable nanopore sequencing for Alzheimer’s research
Video Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
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Using deep long-read RNAseq in Alzheimer’s disease brain to assess clinical relevance of RNA isoform diversity
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The utility of long-read sequencing in diagnosing early-onset Parkinson's disease
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Single-cell long-read whole-genome sequencing reveals somatic transposon activity in human brain
Publication Screening of hidden pathogenic structural variants in PRKN
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Robbing the array to feed the pore: exploring ultra-fast brain tumour diagnosis
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Nanopore sequencing as a novel method of characterising anorexia nervosa risk loci
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Nanopore long-read sequencing as a first-tier diagnostic test to detect repeat expansions in neurological disorders
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Long-read transcriptomic identification of synaptic adaptation to amyloid pathology in the AppNL-G-F knock-in mouse model of the earliest phase of Alz
Video Long-read sequencing to solve exome negative Parkinson's disease
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Long-read sequencing reveals the RNA isoform repertoire of neuropsychiatric risk genes in human brain
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Long-read sequencing reveals the complex splicing profile of the psychiatric risk gene CACNA1C in human brain
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Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
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Long-read genome sequencing and multi-omics in ageing and neurodegeneration
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Long-read epigenetic clocks identify improved brain ageing predictions
Case study Case study: for large-cohort dementia research, nanopore sequencing offers scalability and accessibility
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Integrative analysis of long isoform sequencing and functional data identifies distinct cortical layer neuronal subtypes derived from human iPSCs
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Igniting single-cell analysis of full-length RNA isoforms in brain development
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How ‘Sturgeon’ guides the surgeon