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Workflow overview: NO-MISS
April 16 2026
Publication
Single-molecule cfDNA sequencing establishes clinical utility for ecDNA monitoring and multimodal liquid biopsy analysis
April 9 2026
Publication
Analytical assessment of sgRNA impurities and their impact on functional performance
April 8 2026
Publication
A simplified, scalable solution for simultaneous genotyping of human leukocyte antigen classical class I and human platelet antigen genes
April 6 2026
Publication
Cancer genome standards for long-read sequencing using cancer cell line mixtures
April 3 2026
Video
The African Cancer Atlas: Advancing precision oncology through genomic diversity
April 2 2026
Publication
High-resolution metagenome assembly for modern long reads with myloasm
March 27 2026
Publication
Standalone nanopore sequencing for foodborne pathogen surveillance: a large-scale evaluation and quality control framework
March 24 2026
Publication
Leveraging the Oxford Nanopore MinION sequencing platform for HIV-1 drug resistance surveillance in resource-limited settings
March 15 2026
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Beyond HLA: an adaptive nanopore sequencing assay for simultaneous HLA and blood group profiling in transplantation
March 14 2026
Publication
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
March 12 2026
Video
Unlocking rare diseases with nanopore sequencing
March 10 2026
Publication
Oxford Nanopore enhanced accuracy of long-read amplicons applied to microbial whole-genome sequencing
March 10 2026
Video
Native methylation sequencing for analysis of neurodegenerative conditions
March 10 2026
Video
Nanopore sequencing for clinical research: from critical care to complex genomic signatures
March 10 2026
Poster
Poster: structural and epigenetic profiling of D4Z4 arrays in FSHD using Oxford Nanopore sequencing
March 9 2026
Poster
Poster: DNA extraction from dried blood spots for Oxford Nanopore sequencing
March 9 2026
Publication
Integrated long-read transcriptomic profiling of peripheral blood from ankylosing spondylitis patients identifies regulatory shifts and core genes
March 6 2026
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Identifying intra-hospital Norovirus GII transmission using whole-genome sequencing
March 6 2026
Publication
Assessing mRNA and sgRNA quality for cell and gene therapy applications using nanopore direct RNA sequencing
March 6 2026

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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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Workflow overview: NO-MISS

Single-molecule cfDNA sequencing establishes clinical utility for ecDNA monitoring and multimodal liquid biopsy analysis

Analytical assessment of sgRNA impurities and their impact on functional performance

A simplified, scalable solution for simultaneous genotyping of human leukocyte antigen classical class I and human platelet antigen genes

Cancer genome standards for long-read sequencing using cancer cell line mixtures

The African Cancer Atlas: Advancing precision oncology through genomic diversity

High-resolution metagenome assembly for modern long reads with myloasm

Standalone nanopore sequencing for foodborne pathogen surveillance: a large-scale evaluation and quality control framework

Leveraging the Oxford Nanopore MinION sequencing platform for HIV-1 drug resistance surveillance in resource-limited settings

Beyond HLA: an adaptive nanopore sequencing assay for simultaneous HLA and blood group profiling in transplantation

A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions

Unlocking rare diseases with nanopore sequencing

Oxford Nanopore enhanced accuracy of long-read amplicons applied to microbial whole-genome sequencing

Native methylation sequencing for analysis of neurodegenerative conditions

Nanopore sequencing for clinical research: from critical care to complex genomic signatures

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

Integrated long-read transcriptomic profiling of peripheral blood from ankylosing spondylitis patients identifies regulatory shifts and core genes

Identifying intra-hospital Norovirus GII transmission using whole-genome sequencing

Assessing mRNA and sgRNA quality for cell and gene therapy applications using nanopore direct RNA sequencing

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