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<div class="plainlinks">'''Languages:''' [[Nanopore sequencing|English]] | [[Nanopore sequencing/zh|中文]] | [[Nanopore sequencing/es|español]] | [[Nanopore sequencing/fr|français]] | [[Nanopore sequencing/de|Deutsch]] | [[Nanopore sequencing/ja|日本語]]</div>
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= Nanopore sequencing =
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= Séquençage par nanopores =
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'''Nanopore sequencing''' is a sequencing approach in which individual DNA or RNA molecules pass through nanopores and produce signal changes that can be interpreted as sequence information.
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'''Séquençage par nanopores''' est une approche de séquençage dans laquelle des molécules d'ADN ou d'ARN individuelles passent à travers des nanopores et produisent des changements de signal qui peuvent être interprétés comme des informations de séquence.
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== Features ==
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== Caractéristiques ==
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* Long reads that can help with genome assembly and structural variant detection.
* Real-time data generation and analysis.
* Direct DNA or RNA sensing in many workflows.
* Portable instruments suitable for field and rapid-response settings.
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* Des lectures longues qui peuvent aider à l'assemblage du génome et à la détection des variants structurels.
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* Génération et analyse de données en temps réel.
== Common workflow ==
* Sensation directe de l'ADN ou de l'ARN dans de nombreux flux de travail.
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* Instruments portables adaptés aux paramètres de terrain et de réponse rapide.


== Flux de travail courant ==
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# Sample preparation and library construction.
# Sequencing on a nanopore device.
# Basecalling from raw signal to nucleotide sequence.
# Quality control and filtering.
# Alignment, assembly, variant calling, or metagenomic classification.
# Interpretation and reporting.
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# Préparation de l'échantillon et construction de la bibliothèque.
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# Séquençage sur un dispositif à nanopores.
== Related pages ==
# Conversion des signaux bruts en séquence de nucléotides (basecalling).
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# Contrôle qualité et filtrage.
# Alignement, assemblage, appel de variants ou classification métagenomique.
# Interprétation et rapport.


== Pages connexes ==
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* [[Oxford Nanopore]]
* [[MinION]]
* [[Bioinformatics]]
* [[Glossary]]
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* [[Oxford Nanopore|Oxford Nanopore]]
<languages />
* [[MinION|MinION]]
* [[Bioinformatique]]
* [[Glossaire]]

Revision as of 23:39, 28 June 2026

Nanopore sequencing

Nanopore sequencing is a sequencing approach in which individual DNA or RNA molecules pass through nanopores and produce signal changes that can be interpreted as sequence information.

Features

  • Long reads that can help with genome assembly and structural variant detection.
  • Real-time data generation and analysis.
  • Direct DNA or RNA sensing in many workflows.
  • Portable instruments suitable for field and rapid-response settings.

Common workflow

  1. Sample preparation and library construction.
  2. Sequencing on a nanopore device.
  3. Basecalling from raw signal to nucleotide sequence.
  4. Quality control and filtering.
  5. Alignment, assembly, variant calling, or metagenomic classification.
  6. Interpretation and reporting.
Other languages:
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