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EPI2ME Labs

Publication
Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling
October 3 2025
Workflow
Protocol overview: interaction-free whole-genome sequencing
September 15 2025
Publication
NANOME: a Nextflow pipeline for haplotype-aware allele-specific consensus DNA methylation detection by nanopore long-read sequencing
July 4 2025
Publication
Resolving RH and GYP hybrid alleles while accessing the entire blood group genome with nanopore adaptive sampling
June 11 2025
Publication
Prospective, multicentre validation of a platform for rapid molecular profiling of central nervous system tumours
March 25 2025
Publication
Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases
March 14 2025
Publication
Benchmarking nanopore sequencing and rapid genomics feasibility: validation at a quaternary hospital in New Zealand
November 8 2024
Publication
Telomere-to-telomere phased genome assembly using error-corrected Simplex nanopore reads
May 21 2024
Publication
Single-Cell Omics for Transcriptome CHaracterization (SCOTCH): isoform-level characterisation of gene expression through long-read single-cell RNA seq
April 30 2024
Publication
Biofoundry-scale DNA assembly validation using cost-effective high-throughput long-read sequencing
February 8 2024
Video
NCM 2023 Houston: Enrichment strategies for recovery of Avian influenza virus from samples using MinION
December 6 2023
Publication
Development of a novel streamlined workflow (AACRE) and database (inCREDBle) for genomic analysis of carbapenem-resistant Enterobacterales
November 27 2023
Publication
Clinical application of targeted long read sequencing in prenatal beta-thalassemia testing and genetic counseling
September 23 2023
Video
Core lab webinar series: A new 'gold standard' solution for complete plasmid sequencing
July 28 2023
Publication
Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
July 19 2023
Publication
Evaluating the potential of (epi)genotype-by-low pass nanopore sequencing in dairy cattle: a study on direct genomic value and methylation analysis
July 12 2023
Poster
Targeted long-read sequencing for genetic diversity identification of the zoonotic Cryptosporidium sp.
May 19 2023
Poster
Squiggle analysis for metagenomic viability inference
May 19 2023
Poster
A POretable Metagenomics Pipeline (aPOMP): Fast and Efficient Nanopore sequencing-based metagenomics
May 19 2023
Poster
NanopoReaTA: a user-friendly tool for nanopore-seq real-time transcriptional analysis
May 19 2023

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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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Focus areas

Resource Centre

Single-workflow nanopore whole-genome sequencing with adaptive sampling for accelerated and comprehensive paediatric cancer profiling

Protocol overview: interaction-free whole-genome sequencing

NANOME: a Nextflow pipeline for haplotype-aware allele-specific consensus DNA methylation detection by nanopore long-read sequencing

Resolving RH and GYP hybrid alleles while accessing the entire blood group genome with nanopore adaptive sampling

Prospective, multicentre validation of a platform for rapid molecular profiling of central nervous system tumours

Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases

Benchmarking nanopore sequencing and rapid genomics feasibility: validation at a quaternary hospital in New Zealand

Telomere-to-telomere phased genome assembly using error-corrected Simplex nanopore reads

Single-Cell Omics for Transcriptome CHaracterization (SCOTCH): isoform-level characterisation of gene expression through long-read single-cell RNA seq

Biofoundry-scale DNA assembly validation using cost-effective high-throughput long-read sequencing

NCM 2023 Houston: Enrichment strategies for recovery of Avian influenza virus from samples using MinION

Development of a novel streamlined workflow (AACRE) and database (inCREDBle) for genomic analysis of carbapenem-resistant Enterobacterales

Clinical application of targeted long read sequencing in prenatal beta-thalassemia testing and genetic counseling

Core lab webinar series: A new 'gold standard' solution for complete plasmid sequencing

Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer

Evaluating the potential of (epi)genotype-by-low pass nanopore sequencing in dairy cattle: a study on direct genomic value and methylation analysis

Targeted long-read sequencing for genetic diversity identification of the zoonotic Cryptosporidium sp.

Squiggle analysis for metagenomic viability inference

A POretable Metagenomics Pipeline (aPOMP): Fast and Efficient Nanopore sequencing-based metagenomics

NanopoReaTA: a user-friendly tool for nanopore-seq real-time transcriptional analysis

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