PreciseMedicine

Deliver the appropriate treatment to each patient.
Eliminate trial-and-error prescriptions.
PolygenDx can be performed on either a single sample or a cohort of thousands of individuals.
All that's required is a file containing genome-wide genetic variants, such as:
  • VCF / BCF files
  • Plink files (Coming Soon)
  • 23andMe format files (Coming Soon)
  • BAM / CRAM Files (Coming Soon)
  • PolygenDx
    PolygenDx

    A PolygenRx platform to explore precision medicine.

    Services

    PolygenDx

    PolygenEx - Coming soon

    PolygenRx

    Useful links

    About

    Terms and conditions

    Contact

    Contact

    Callaghan, 2308, NSW, Australia

    contact@polygenrx.com

    +61 (0) 1 23 456 789

    © 2024 PolygenRx