Molecular pathology.
Personalized.

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Because the global fight against cancer requires the best personalized molecular detection tools to get the right answer the first time

Sample-to-certainty targeted sequencing

NGS implementation goes far beyond sequencing. With trusted assay development capabilities, best in class molecular detection technology and purpose-built genomics analysis platform, we take you from a question to an answer you can be confident in.
Simply solving the most complex genomic problems

Archer library preparation assays are simple and work from low-input FFPE samples to provide
- Novel gene fusion detection
- Sensitive variant detection
- Robust CNV and expression information
Purpose-built analysis and integrated genomics platform
- Powerful analysis for unprecedented data quality
- Simple, intuitive user experience
- Workflow management and systems integration
- Flexible and secure local or cloud-based deployment
Scalable and flexible NGS implementation

Any of Archer’s custom or off-the-shelf assays are able to have new genes added to them without impacting assay performance. Adoption of Archer assays enables future growth based on new discoveries.
Companion diagnostic development

With the best detection technology, a global reach and ISO13485 design control, Archer is the preferred NGS CDx partner.