ArcherDX combines targeted NGS library preparation kits and powerful bioinformatics software to detect gene fusions, point mutations and CNVs in clinical sample types
Comprehensive and disease-specific NGS panels powered by Anchored Multiplex PCR (AMP™) to detect known and novel fusions, point mutations and relative expression levels from RNA and copy number variations including FLT3 internal tandem repeats from DNA. Kits include:
Characterization of B- and T-Cell Immune Repertoires by Anchored Multiplex PCR and Next-Generation Sequencing
To address the existing bottlenecks of using NGS in translational research, we’ve created a robust platform that is purpose-built for clinical oncology research.
By combining revolutionary Anchored Multiplex PCR (AMP™) chemistry with an easy-to-use workflow and intuitive software, we are unleashing the power of translational NGS to enable accurate and scalable mutation detection.
2477 55th Street, Suite 202
Boulder, CO 80301