Accelerate biopharmaceutical development with a single sequencing platform that replaces fragmented assays — delivering full-length, real-time multidimensional insights from discovery through to good manufacturing practice (GMP)-ready quality control (QC).
Oxford Nanopore sequencing is a single-platform solution for your entire pipeline, so you can simplify workflows, reduce risk, stay compliant with confidence, and make fast decisions. Reveal the full molecular picture of plasmid constructs, viral vectors, mRNA therapeutics, and more.
What sets Oxford Nanopore apart?
- Replace multiple assays with a single QC test
- Generate full-length sequence data in real time
- Verify construct and therapeutic identity, integrity, and purity with confidence
One solution — from R&D to QC
Accuracy you can trust — insight you can act on
Cell and gene therapy development is inherently complex. Discover how comprehensive nanopore sequencing acts as a critical checkpoint at every stage, providing you with the data you need to develop better and safer drugs.
Compliance built in. Confidence delivered.
Learn how the Oxford Nanopore QC Test Packs for plasmid and mRNA critical quality attribute (CQA) testing provide everything you need to successfully deploy in GMP environments.
'Nanopore sequencing enabled our scalable, end-to-end quality control pipeline throughout the whole production of our recombinant AAV vectors'
Stefan Hardy Lung
Institute of Virology Innsbruck, Austria
Explore resources
Unlocking the biopharma development pipeline with Oxford Nanopore
A guide to biopharma solutions from Oxford Nanopore
Rapid and complete plasmid characterisation with Oxford Nanopore sequencing
Q-Line: sequencing in regulated environments
Q-Line is a range of sequencing products designed to support regulated GMP environments. It delivers real-time nanopore sequencing in a standardised, tightly controlled format, supporting seamless and scalable transfer of analytical methods from discovery to commercialisation.
Discover the Q-Line GridION
Five MinION Flow Cells can be operated individually or together
Industry-specific software supporting 21 CFR Part 11 and EU GMP Annex 11 configuration
Onboard data analysis
Pre-configure run settings for specific QC assays