Resource centre

Main menu

456 results

Cancer research

Workflow
Workflow overview: tumour-normal sequencing
July 21 2025
Workflow
Workflow overview: single-cell transcriptomics
February 24 2025
Workflow
Workflow overview: Hereditary Cancer Panel
January 20 2026
Workflow
Workflow overview: human variant calling
April 29 2025
Workflow
Workflow overview: bulk transcriptomics
July 28 2025
Publication
The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology
January 23 2024
Publication
Whole genome sequencing reveals virulence potentials of Helicobacter pylori strain KE21 isolated from a Kenyan patient with gastric signet ring cell carcinoma
August 29 2020
Publication
Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer
April 29 2021
Video
Whole-genome insights: nanopore sequencing in neuropathology
May 19 2025
Publication
Whole genome assembly of human papillomavirus by nanopore long-read sequencing
January 4 2022
Video
Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing
November 18 2025
Webinar
Transforming hereditary cancer sequencing with adaptive sampling target enrichment
November 11 2025
Video
Resolving complex genomic structures and regulation patterns in cervical cancer
April 11 2023
Video
Webinar: Rapid leukemia classification using nanopore sequencing
October 7 2022
Video
Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants
June 26 2023
Video
Nanopore sequencing: insights from neonatal intensive care to cancer
November 15 2023
Video
Investigating epigenomic alterations in cancer with nanopore sequencing
October 11 2022
Video
Detecting, classifying, and monitoring CNS tumors with nanopore sequencing
July 14 2023
Video
Analysing complex somatic rearrangements in cancer using nanopore sequencing
December 15 2022
Video
Advancing long-read de novo genome assembly methods in clinical research
September 15 2022

Getting started

Buy a MinION starter pack Nanopore store Sequencing service providers Channel partners

Quick links

Intellectual property Cookie policy Corporate reporting Privacy policy Terms, conditions and policies Accessibility

About Oxford Nanopore

© 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.

ONT plc is a member of the producer compliance scheme run by ERP UK Ltd, who manage the submission of documentation in support of WEEE compliance for ONT plc’s manufacture and supply of Electrical and Electronic equipment in the UK.

ONT’s WEEE PRN is WEE/MM3828AA. See attached certificate for the submission period 2022.

Select Language

Focus areas

Resource Centre

Workflow overview: tumour-normal sequencing

Workflow overview: single-cell transcriptomics

Workflow overview: Hereditary Cancer Panel

Workflow overview: human variant calling

Workflow overview: bulk transcriptomics

The whole is greater than the sum of its parts: long-read sequencing for solving clinical problems in haematology

Whole genome sequencing reveals virulence potentials of Helicobacter pylori strain KE21 isolated from a Kenyan patient with gastric signet ring cell carcinoma

Whole-genome sequencing with long reads reveals complex structure and origin of structural variation in human genetic variations and somatic mutations in cancer

Whole-genome insights: nanopore sequencing in neuropathology

Whole genome assembly of human papillomavirus by nanopore long-read sequencing

Transforming tumor methylation profiling with Oxford Nanopore direct DNA sequencing

Transforming hereditary cancer sequencing with adaptive sampling target enrichment

Resolving complex genomic structures and regulation patterns in cervical cancer

Webinar: Rapid leukemia classification using nanopore sequencing

Parent-of-origin-aware genomic analysis infers segregation of pathogenic variants

Nanopore sequencing: insights from neonatal intensive care to cancer

Investigating epigenomic alterations in cancer with nanopore sequencing

Detecting, classifying, and monitoring CNS tumors with nanopore sequencing

Analysing complex somatic rearrangements in cancer using nanopore sequencing

Advancing long-read de novo genome assembly methods in clinical research

Filter

Products

Research areas

Techniques