NTRK fusions are critical events in cancer biology notoriously difficult-to-detect known and unknown fusion partners.
Archer FusionPlex® NGS assays provide sensitive NTRK fusion detection without prior knowledge of breakpoints or fusion partners.
|Low input requirement|
|Recurrent fusion detection|
|Novel fusion detection|
|Rapid turnaround time|
|Low cost to adopt|
RNA-based, low-input, FFPE-compatible next-generation sequencing library preparation kits and analysis software with the following features:
Detect and identify gene fusions without prior knowledge of breakpoints or fusion partners by using the most advanced fusion detection technology available.
Minimize turnaround time with our simple lyophilized reagent workflow, optimized for high-volume labs. The streamlined workflow reduces chances of contamination and error in library preparation.
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.
Create a new assay or add to an
existing panel with Archer Assay Designer
2477 55th Street, Suite 202
Boulder, CO 80301