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Poster: structural and epigenetic profiling of D4Z4 arrays in FSHD using Oxford Nanopore sequencing
March 9 2026
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Poster: DNA extraction from dried blood spots for Oxford Nanopore sequencing
March 9 2026
Poster
Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels
November 11 2025
Poster
Resolving challenging medically-relevant genes using nanopore sequencing
October 14 2025
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A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing
October 14 2025
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Comprehensive resolution of challenging genomic variation with Oxford Nanopore telomere-to-telomere assemblies
October 14 2025
Poster
An end-to-end workflow for pharmacogenomic target enrichment, star allele annotation, and CYP2D6 resolution using nanopore sequencing
October 14 2025
Poster
Validation and quality control of a molecular cloning experiment using de novo assembly of Oxford Nanopore reads
May 20 2025
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Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing
May 20 2025
Poster
Single-cell transcriptomics with full-length cDNA sequencing provides unique insights into cellular diversity
May 20 2025
Poster
Resolving challenging medically relevant genes of the human genome with native Oxford Nanopore reads
May 20 2025
Poster
Rapid whole-genome sequencing, de novo assembly, and characterisation of bacterial isolates
May 20 2025
Poster
Quick and simple analysis of PCR products with Oxford Nanopore reads
May 20 2025
Poster
Open access Oxford Nanopore datasets for reproducible benchmarking, sequence exploration, and testing
May 20 2025
Poster
Multiomic data identifies skewed X-inactivation and its role in masking Mendelian inheritance patterns
May 20 2025
Poster
Multiomics whole-genome characterisation of a cancer genome using Oxford Nanopore sequencing
May 20 2025
Poster
Genomic insights into the biology of complex microbiomes with Oxford Nanopore metagenomic sequencing
May 20 2025
Poster
An end-to-end workflow for pharmacogenomic target enrichment, star allele annotation, and CYP2D6 resolution
May 20 2025
Poster
EPI2ME end-to-end workflows for biopharma quality control of plasmids and mRNA
May 20 2025
Poster
EPI2ME – an extensible product for applied bioinformatics
May 20 2025

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© 2008 - 2026 Oxford Nanopore Technologies plc. All rights reserved. Registered Office: Gosling Building, Edmund Halley Road, Oxford Science Park, OX4 4DQ, UK | Registered No. 05386273 | VAT No 336942382. Oxford Nanopore Technologies, the Wheel icon, AmPORE-TB, EPI2ME, GridION, MinION, MinKNOW, PromethION, P2 Solo, and P2 are registered trademarks or the subject of trademark applications of Oxford Nanopore Technologies plc in various countries. Information contained herein may be protected by copyright, patents or patents pending of Oxford Nanopore Technologies plc. All other brands and names contained are the property of their respective owners. Oxford Nanopore Technologies products are RUO. Products labelled/branded as Oxford Nanopore Diagnostics may be RUO or may be regulated as in‐vitro diagnostic devices in some jurisdictions, please check individual product labelling.

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Poster: structural and epigenetic profiling of D4Z4 arrays in FSHD using Oxford Nanopore sequencing

Poster: DNA extraction from dried blood spots for Oxford Nanopore sequencing

Scalable pharmacogenomics (PGx) using targeted long-read genotyping panels

Resolving challenging medically-relevant genes using nanopore sequencing

A multi-omic investigation of gene dysregulation in a complex chromothripsis-like translocation event using Oxford Nanopore sequencing

Comprehensive resolution of challenging genomic variation with Oxford Nanopore telomere-to-telomere assemblies

An end-to-end workflow for pharmacogenomic target enrichment, star allele annotation, and CYP2D6 resolution using nanopore sequencing

Validation and quality control of a molecular cloning experiment using de novo assembly of Oxford Nanopore reads

Transcriptome-wide expression and RNA modifications with full-length native RNA and cDNA sequencing

Single-cell transcriptomics with full-length cDNA sequencing provides unique insights into cellular diversity

Resolving challenging medically relevant genes of the human genome with native Oxford Nanopore reads

Rapid whole-genome sequencing, de novo assembly, and characterisation of bacterial isolates

Quick and simple analysis of PCR products with Oxford Nanopore reads

Open access Oxford Nanopore datasets for reproducible benchmarking, sequence exploration, and testing

Multiomic data identifies skewed X-inactivation and its role in masking Mendelian inheritance patterns

Multiomics whole-genome characterisation of a cancer genome using Oxford Nanopore sequencing

Genomic insights into the biology of complex microbiomes with Oxford Nanopore metagenomic sequencing

An end-to-end workflow for pharmacogenomic target enrichment, star allele annotation, and CYP2D6 resolution

EPI2ME end-to-end workflows for biopharma quality control of plasmids and mRNA

EPI2ME – an extensible product for applied bioinformatics

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