Main menu

Get comprehensive whole-genome analysis on a single platform

Whole-genome sequencing aims to provide complete analysis of an organism’s genome, but legacy short-read sequencing technologies are known to miss many important genomic regions and variants — even in the exome.

Oxford Nanopore sequencing, with its capacity to produce ultra-long reads (exceeding 4 Mb), can span complex structural variants (SVs) and repeat regions that legacy technologies cannot access, while the facility to directly sequence native DNA (and RNA), without amplification, further enables simultaneous detection of epigenetic modifications alongside the nucleotide sequence to deliver deeper genomic insights.

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

お問い合わせ

Intellectual property Cookie policy Corporate reporting Privacy policy Terms & conditions Accessibility

Oxford Nanoporeについて

Contact us 経営陣 メディアリソース & お問い合わせ先 投資家向け Oxford Nanopore社で働く BSI 27001 accreditationBSI 90001 accreditationBSI mark of trust
Japanese flag