Main menu

Detecting isoforms and RNA modifications with PCR-free, direct RNA nanopore sequencing


The direct RNA sequencing workflow

Overview

Accurately capturing the range of RNA diversity can help elucidate the molecular mechanisms of disease and functional roles of RNA modifications. Nanopore sequencing is the only available technology that directly reads native RNA transcripts, enabling quantitation of gene and isoform expression without PCR bias along with direct RNA methylation detection.

This end-to-end workflow overview provides a simple method to characterise RNA modifications from a human blood research sample using direct RNA sequencing.

In this workflow, you will:

  • Find out how direct RNA sequencing enhances isoform and RNA modification detection
  • Discover our best practice sequencing workflow in detail, starting from the recommended extraction method, through to primary analysis
  • Learn about our recommended sequencing kit and devices

入門

MinION Starter Packを購入 ナノポア製品の販売 シークエンスサービスプロバイダー グローバルディストリビューター

ナノポア技術

ナノポアの最新ニュースを購読 リソースと発表文献 Nanopore Communityとは

Oxford Nanoporeについて

ニュース 会社沿革 持続可能性 経営陣 メディアリソース & お問い合わせ先 投資家向け パートナー向け Oxford Nanopore社で働く 現在の募集状況 営業上の情報 BSI 27001 accreditationBSI 90001 accreditationBSI mark of trust
Japanese flag