2016 American Society of Hemotology Annual Meeting

December 3-6, 2016 | San Diego, California
Booth #1606





ArcherDX combines targeted NGS library preparation kits and powerful bioinformatics software to detect gene fusions, point mutations and CNVs in clinical sample types

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Featuring

Blood cancer logo

Archer Blood Cancer NGS Assays

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:

  • Heme v2 Kit
  • Myeloid Kit
  • ALL Kit
  • Lymphoma Kit
  • Pan-Heme Kit
  • Core AML Kit
Learn more!
Immunoverse logo

Immune repertoire sequencing assays

Characterization of B- and T-Cell Immune Repertoires by Anchored Multiplex PCR and Next-Generation Sequencing

  • Molecular barcode-based error correction
  • High sensitivity for rare clone identification
  • Unbiased amplification for true and reproducible measure of diversity
  • Transparent and user-owned analysis
  • Wide range of input quantities
Learn more!

About ArcherDX

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.



How to contact us

Address

2477 55th Street, Suite 202

Boulder, CO 80301

Phone

Phone: (877) 771 1093

Phone: (303) 357 9001

All content © 2018 ArcherDX, Inc.

For Research Use Only. Not for use in diagnostic procedures. For Research Use Only. Not for use in diagnostic procedures.