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[[File:Oxford Nanopore MinION side.jpg|thumb|right|320px|Oxford Nanopore MinION portable sequencer. Source: Wikimedia Commons, CC BY-SA 4.0.]]
[[File:Oxford Nanopore MinION side.jpg|thumb|right|320px|Oxford Nanopore MinION portable sequencer. Source: Wikimedia Commons, CC BY-SA 4.0.]]
'''Oxford Nanopore''' is part of the Nanopore Wiki learning path. Oxford Nanopore Technologies develops nanopore sequencing instruments, flow cells, chemistry, and software for real-time DNA and RNA sequencing.
'''Oxford Nanopore''' is part of the Wiki learning path. Oxford Nanopore Technologies develops nanopore sequencing instruments, flow cells, chemistry, and software for real-time DNA and RNA sequencing.


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Revision as of 11:42, 30 June 2026

File:Oxford Nanopore MinION side.jpg
Oxford Nanopore MinION portable sequencer. Source: Wikimedia Commons, CC BY-SA 4.0.

Oxford Nanopore is part of the Wiki learning path. Oxford Nanopore Technologies develops nanopore sequencing instruments, flow cells, chemistry, and software for real-time DNA and RNA sequencing.

Core concepts

  • The platform reads electrical signals produced as molecules pass through nanopores.
  • Device families include portable and higher-throughput instruments.
  • Output can include raw signal files, basecalled reads, alignments, and analysis reports.
  • Performance depends on chemistry, flow cell quality, library preparation, basecaller model, and analysis settings.

Typical sequencing workflow

Step Description
1 Prepare DNA or RNA library according to the assay.
2 Load library onto a flow cell and start sequencing.
3 Basecall raw signal into sequence reads and quality scores.
4 Run quality control, alignment, assembly, variant calling, modification calling, or classification.

Typical applications

  • Long-read genome sequencing.
  • Metagenomics and pathogen surveillance.
  • Transcriptomics and direct RNA sequencing.
  • Structural variant and modification detection.

Common pitfalls

  • Comparing results without chemistry and model versions.
  • Ignoring read quality, pore count, run yield, and sample degradation.
  • Presenting research use as clinical guidance without validation.

References