NTRK Fusion Detection

NTRK fusions are critical events in cancer genomics and are notoriously difficult to detect. Archer® FusionPlex® next-generation sequencing (NGS) tests provide sensitive NTRK fusion detection without prior knowledge of fusion partners.

NGS Library preparation methods for fusion detection

RNA-based
amplicon

DNA-based
hybrid capture

RNA-based
hybrid capture

FusionPlex assay (RNA)
Low input requirement
Recurrent fusion detection
Novel fusion detection
Sensitivity
Simple workflow
Rapid turn-around time
Low cost to adopt
Customizable

Archer FusionPlex NGS Assays

Assays

Detect and identify gene fusions without prior knowledge of fusion partners by using patented fusion detection technology.

Workflow

Minimize turn-around time with our simple lyophilized reagent workflow, optimized for high-volume labs. The streamlined workflow reduces chances of contamination and error in library preparation.

Analysis

Be confident in your results by using the comprehensive Archer Analysis. A simple user interface provides in-line visualization and clear reporting. Analysis also allows for third party integration and deploys securely to the cloud or on a local server.

NTRK-CONTAINING

FusionPlex Panels

  • 75 Genes
  • 3M Reads
  • 53 Genes
  • 3M Reads
  • 36 Genes
  • 1.5M Reads
  • 14 Genes
  • .5M Reads

Build your own or modify any of the above assays.

  • 4-5 Weeks
Get Started With

FusionPlex NGS Assays

Contact your Archer representative today

Ask about our starter panels and wet lab training by Archer field scientists.

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