Main menu

Precision genomics for hereditary cancer with adaptive sampling

The Oxford Nanopore Hereditary Cancer Panel offers comprehensive germline variant analysis across 258 cancer predisposition genes. The panel uses adaptive sampling: a fast and flexible on-sequencer target enrichment methodology. No lengthy library preparation, baits, or primers required.

Why choose the Oxford Nanopore Hereditary Cancer Panel?

  • One consolidated assay for deeper genomic and epigenomic insight — in one go.

  • Rapid, streamlined sequencing — no batching required

  • Flexible enrichment. Scalable sequencing. Built for every lab.

HCP workflow figure
Recommended device for the Hereditary Cancer Panel

PromethION 24

The PromethION 24 (P24) is a high-throughput sequencing device featuring 24 independent flow cells positions, allowing users to sequence multiple samples simultaneously or flexibly scale their experiments.

PromethION 24 Sequencing device

Heading

Aliquip error vestibulum, purus sapiente aliqua reprehenderit ullamcorper, condimentum aut proident nostrum tellus felis varius, minim sapien deleniti tempor voluptates error taciti? Officia tempor error hic orci condimentum aute commodi wisi tenetur natus ea, atque! Integer animi vestibulum laboriosam, alias mus sapiente justo aliquet repudiandae urna? Minima erat? Omnis sodales.

Aspernatur a facilisi faucibus sem unde potenti expedita. Curabitur, dui dis erat iste natoque! Modi, quis est luctus! Aute eligendi corrupti at pharetra facilisi, tempora posuere class reiciendis minima hendrerit, leo do aperiam, lacus quam veritatis, malesuada varius cupidatat a eum curabitur est possimus facere dignissimos penatibus augue, inventore imperdiet.

Aliquip error vestibulum, purus sapiente aliqua reprehenderit ullamcorper, condimentum aut proident nostrum tellus felis varius, minim sapien deleniti tempor voluptates error taciti? Officia tempor error hic orci condimentum aute commodi wisi tenetur natus ea, atque! Integer animi vestibulum laboriosam, alias mus sapiente justo aliquet repudiandae urna? Minima erat? Omnis sodales.

Aspernatur a facilisi faucibus sem unde potenti expedita. Curabitur, dui dis erat iste natoque! Modi, quis est luctus! Aute eligendi corrupti at pharetra facilisi, tempora posuere class reiciendis minima hendrerit, leo do aperiam, lacus quam veritatis, malesuada varius cupidatat a eum curabitur est possimus facere dignissimos penatibus augue, inventore imperdiet.

Aliquip error vestibulum, purus sapiente aliqua reprehenderit ullamcorper, condimentum aut proident nostrum tellus felis varius, minim sapien deleniti tempor voluptates error taciti? Officia tempor error hic orci condimentum aute commodi wisi tenetur natus ea, atque! Integer animi vestibulum laboriosam, alias mus sapiente justo aliquet repudiandae urna? Minima erat? Omnis sodales.

Aspernatur a facilisi faucibus sem unde potenti expedita. Curabitur, dui dis erat iste natoque! Modi, quis est luctus! Aute eligendi corrupti at pharetra facilisi, tempora posuere class reiciendis minima hendrerit, leo do aperiam, lacus quam veritatis, malesuada varius cupidatat a eum curabitur est possimus facere dignissimos penatibus augue, inventore imperdiet.

Aliquip error vestibulum, purus sapiente aliqua reprehenderit ullamcorper, condimentum aut proident nostrum tellus felis varius, minim sapien deleniti tempor voluptates error taciti? Officia tempor error hic orci condimentum aute commodi wisi tenetur natus ea, atque! Integer animi vestibulum laboriosam, alias mus sapiente justo aliquet repudiandae urna? Minima erat? Omnis sodales.

Aspernatur a facilisi faucibus sem unde potenti expedita. Curabitur, dui dis erat iste natoque! Modi, quis est luctus! Aute eligendi corrupti at pharetra facilisi, tempora posuere class reiciendis minima hendrerit, leo do aperiam, lacus quam veritatis, malesuada varius cupidatat a eum curabitur est possimus facere dignissimos penatibus augue, inventore imperdiet.

Application note: Hereditary Cancer Panel — 2 pages

Comprehensive genomic and epigenomic profiling with the Oxford Nanopore Hereditary Cancer Panel

This application note highlights how the HCP provides a scalable, accessible, and cost-effective solution for comprehensive analysis of hereditary cancer genes, with the potential to advance precision oncology.

Getting started

Buy a MinION starter pack Nanopore store Sequencing service providers Channel partners

Quick links

Intellectual property Cookie policy Corporate reporting Privacy policy Terms, conditions and policies Modern slavery policy Accessibility

About Oxford Nanopore

Contact us News Media resources & contacts Investor centre Careers BSI 27001 accreditationBSI 90001 accreditationBSI mark of trust
Spanish flag