Revision as of 23:06, 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>
-= ナノポアシークエンシング =
+<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>
-'''ナノポアシークエンシング'''は、個々のDNAやRNA分子がナノポアを通過し、その信号の変化をシークエンス情報として解釈するシークエンシング手法です。
+<div lang="en" dir="ltr" class="mw-content-ltr">
+== Features ==
+</div>
-== 特徴 ==
+<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>
-* ゲノムアセンブリや構造変異検出に役立つ長いリード。
+<div lang="en" dir="ltr" class="mw-content-ltr">
-* リアルタイムのデータ生成と分析。
+== Common workflow ==
-* 多くのワークフローで直接DNAやRNAを検出。
+</div>
-* 携帯可能な機器で、現場や迅速な対応に適しています。
-== 一般的なワークフロー ==
+<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>
-# サンプル準備とライブラリ構築。
+<div lang="en" dir="ltr" class="mw-content-ltr">
-# ナノポアデバイスでのシークエンシング。
+== Related pages ==
-# 生の信号からヌクレオチドシークエンスへのベースコール。
+</div>
-# 品質管理とフィルタリング。
-# アライメント、アセンブリ、変異コール、またはメタゲノム分類。
-# 解釈と報告。
-== 関連ページ ==
+<div lang="en" dir="ltr" class="mw-content-ltr">
+* [[Oxford Nanopore]]
+* [[MinION]]
+* [[Bioinformatics]]
+* [[Glossary]]
+</div>
-* [[Oxford Nanopore|Oxford Nanopore]]
+<languages />
-* [[MinION|MinION]]
-* [[Bioinformatics|バイオインフォマティクス]]
-* [[Glossary|用語集]]