Resource Centre
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Pre-phasing long reads improves structural variant genotyping
- Phasing
- Bioinformatics
- Structural variation
October 24 2025
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Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic
- Phasing
- Bioinformatics
- Cancer research
- Variant calling
- PromethION 24/48
October 16 2025
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Resolving challenging medically-relevant genes using nanopore sequencing
- Phasing
- Clinical research
- Variant calling
- Human genomics
October 14 2025
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Integrating long-read nanopore sequencing for precision resolution of genomic variants in dystonia
- Phasing
- Human genomics
- Methylation
- Structural variation
- SNVs
- PromethION 24/48
September 30 2025
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A complete diploid human genome benchmark for personalised genomics
- Phasing
- Human genomics
- Whole genome
- Long-read
September 21 2025
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Getting started guide: human genomics
- Phasing
- Human genomics
- Clinical research
- Whole genome
- Targeted
- Structural variation
September 17 2025
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Workflow overview: pharmacogenomics with adaptive sampling
- Phasing
- Pharmacogenomics
- Biopharma
- Human genomics
- Clinical research
- Targeted
August 5 2025
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Long-read genome sequencing enhances diagnostics of paediatric neurological disorders
- Phasing
- Human genomics
- Methylation
- Neuroscience
- Structural variation
- PromethION 24/48
June 24 2025
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Resolving RH and GYP hybrid alleles while accessing the entire blood group genome with nanopore adaptive sampling
- Phasing
- Human genomics
- Clinical research
- Adaptive sampling
- SNVs
- Structural variation
June 11 2025
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Multiomic data identifies skewed X-inactivation and its role in masking Mendelian inheritance patterns
- Phasing
- London Calling
- Human genomics
- Methylation
May 20 2025
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End-to-end workflow for haplotype-resolved genetic and epigenetic variant calling using Oxford Nanopore sequencing
- Phasing
- London Calling
- Methylation
- Structural variation
May 20 2025
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Variant phasing for antisense oligonucleotide design using adaptive sampling
- Phasing
- Phasing
- PromethION 24/48
- Targeted
- Human genomics
- PromethION 24/48
May 19 2025
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Using ultra-long-read Oxford Nanopore sequencing to detect complex structural variants in leukaemia
- Phasing
- Phasing
- MinION
- PromethION 2
- Structural variation
- Targeted
May 19 2025
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Nanopore-based HLA testing: a rising star driving real-world clinical implementation in pharmacogenomics
- Phasing
- Cancer research
- Clinical research
- Education
- Infectious disease
- MinION
May 19 2025
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Masterclass: How to call variants and methylation across the human genome | LC25
- Phasing
- Human genomics
- Clinical research
- Population genomics
- Bioinformatics
- PromethION 2
May 19 2025
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Masterclass: How to analyse your Oxford Nanopore sequencing data | LC25
- Phasing
- EPI2ME
- Assembly
- Epigenetics
- Metagenomics
- Multiomics
May 19 2025
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Long-read sequencing of an advanced cancer cohort
- Phasing
- Phasing
- PromethION 24/48
- EPI2ME
- Epigenetics
- Structural variation
May 19 2025
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Great Barrier Reef Microbial Genomes Database: enhanced recovery of prokaryote, viral, and T2T eukaryote genomes
- Phasing
- Phasing
- MinION
- PromethION 2
- Assembly
- Epigenetics
May 19 2025
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Cornetto: adaptively integrated nanopore sequencing and genome assembly
- Phasing
- PromethION 2
- PromethION 24/48
- Assembly
- Structural variation
- Whole genome
May 19 2025
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Comprehensive characterisation of the FCGR locus using Oxford Nanopore sequencing to enhance immunotherapy efficacy
- Phasing
- Phasing
- MinION
- GridION
- PromethION 2
- Assembly
May 19 2025
