Revision as of 23:45, 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

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.

@@ Line 1: / Line 1: @@
-<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>
+<div lang="en" dir="ltr" class="mw-content-ltr">
+= Nanopore sequencing =
+</div>
-= Secuenciación por nanoporo =
+<div lang="en" dir="ltr" class="mw-content-ltr">
+'''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.
+</div>
-'''Secuenciación por nanoporo''' es un enfoque de secuenciación en el que las moléculas de ADN o ARN individuales pasan a través de nanoporos y producen cambios de señal que pueden interpretarse como información de secuencia.
+<div lang="en" dir="ltr" class="mw-content-ltr">
+== Features ==
+</div>
-== Características ==
+<div lang="en" dir="ltr" class="mw-content-ltr">
+* 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.
+</div>
-* Lecturas largas que pueden ayudar con la ensamblaje del genoma y la detección de variantes estructurales.
+<div lang="en" dir="ltr" class="mw-content-ltr">
-* Generación y análisis de datos en tiempo real.
+== Common workflow ==
-* Sensado directo de ADN o ARN en muchos flujos de trabajo.
+</div>
-* Instrumentos portátiles adecuados para entornos de campo y respuesta rápida.
-== Flujo de trabajo común ==
+<div lang="en" dir="ltr" class="mw-content-ltr">
+# 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.
+</div>
-# Preparación de la muestra y construcción de la biblioteca.
+<div lang="en" dir="ltr" class="mw-content-ltr">
-# Secuenciación en un dispositivo de nanoporo.
+== Related pages ==
-# Conversión de la señal cruda a secuencia de nucleótidos.
+</div>
-# Control de calidad y filtrado.
-# Alineamiento, ensamblaje, llamada de variantes o clasificación metagenómica.
-# Interpretación y reporte.
-== Páginas relacionadas ==
+<div lang="en" dir="ltr" class="mw-content-ltr">
+* [[Oxford Nanopore]]
+* [[MinION]]
+* [[Bioinformatics]]
+* [[Glossary]]
+</div>
-* [[Oxford Nanopore|Oxford Nanopore]]
+<languages />
-* [[MinION|MinION]]
-* [[Bioinformática]]
-* [[Glosario]]