Resource Centre
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Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels
- Pharmacogenomics
- Human genomics
- Targeted
- Methylation
November 11 2025
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Resolving challenging medically-relevant genes using nanopore sequencing
- Clinical research
- Variant calling
- Human genomics
- Phasing
October 14 2025
A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
- Human genomics
- Clinical research
- Assembly
- cDNA
- Multiomics
October 14 2025
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Comprehensive resolution of challenging genomic variation with Oxford Nanopore telomere-to-telomere assemblies
- Assembly
- Variant calling
- Clinical research
- Human genomics
- Structural variation
October 14 2025
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An end-to-end workflow for pharmacogenomic target enrichment, star allele annotation, and CYP2D6 resolution using nanopore sequencing
- Pharmacogenomics
- Human genomics
- Targeted
- Methylation
October 14 2025
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Validation and quality control of a molecular cloning experiment using de novo assembly of Oxford Nanopore reads
- London Calling
- EPI2ME
- Plasmid
May 20 2025
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Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
- London Calling
- cDNA
- RNA
- Transcriptomics
May 20 2025
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Single-cell transcriptomics with full-length cDNA sequencing provides unique insights into cellular diversity
- Single cell
- Cancer research
- London Calling
May 20 2025
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Resolving challenging medically relevant genes of the human genome with native Oxford Nanopore reads
- London Calling
- Structural variation
- Human genomics
May 20 2025
Rapid whole-genome sequencing, de novo assembly, and characterisation of bacterial isolates
- EPI2ME
- London Calling
- Bacteria
May 20 2025
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Quick and simple analysis of PCR products with Oxford Nanopore reads
- Targeted
- EPI2ME
- London Calling
May 20 2025
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Open access Oxford Nanopore datasets for reproducible benchmarking, sequence exploration, and testing
- Data release
- EPI2ME
- London Calling
May 20 2025
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Multiomic data identifies skewed X-inactivation and its role in masking Mendelian inheritance patterns
- London Calling
- Phasing
- Human genomics
- Methylation
May 20 2025
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Multiomics whole-genome characterisation of a cancer genome using Oxford Nanopore sequencing
- London Calling
- Cancer research
- Methylation
- Variant calling
May 20 2025
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Genomic insights into the biology of complex microbiomes with Oxford Nanopore metagenomic sequencing
- London Calling
- Microbiology
- Metagenomics
- Assembly
May 20 2025
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An end-to-end workflow for pharmacogenomic target enrichment, star allele annotation, and CYP2D6 resolution
- London Calling
- GridION
- PromethION 24/48
- Pharmacogenomics
May 20 2025
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EPI2ME end-to-end workflows for biopharma quality control of plasmids and mRNA
- Biopharma
- EPI2ME
- London Calling
May 20 2025
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EPI2ME – an extensible product for applied bioinformatics
- London Calling
- EPI2ME
- Bioinformatics
May 20 2025
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End-to-end workflow for haplotype-resolved genetic and epigenetic variant calling using Oxford Nanopore sequencing
- London Calling
- Phasing
- Methylation
- Structural variation
May 20 2025
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Easy transfer of routine, day-to-day sequencing applications to the Oxford Nanopore platform
- EPI2ME
- Workflow
- London Calling
May 20 2025
