Panorama is a Non-Invasive Prenatal Test (NIPT) that screens for common genetic conditions caused by extra or missing chromosomes in the baby’s DNA as early as 9 weeks. Panorama analyzes baby's (placental) DNA through a simple blood draw from the mother’s arm.

The Counsyl Family Prep Screen identifies parents-to-be that are likely to pass on genetic- conditions to their children. Even without a family history of disease, you can still be a carrier and benefit from this test, which screens for over 175 conditions before or during pregnancy.

TreatGx ^Plus predicts your response to medications by analyzing medication-to-medication, medication-to-disease, and medication-to-genetic interactions. This personalized analysis leads to ideal medication and dosage options for you, so that safer and more effective medications can be prescribed

More and more Canadians with early cancer diagnoses or pronounced family histories of breast or ovarian cancers are considering BRCA1 and BRCA2 (BRCA1/2) genetic testing.

To determine a cause for a complex genetic disorder, WES analyzes thousands of genes simultaneously, providing an alternative to single-gene tests or multigene panels to investigate the molecular basis of genetic disorders.

WGS is one of the latest genetic technologies that sequences the entire coding and non-coding regions of the genome to help provide answers for individuals with complex disease where other tests have not.

These 3500+ diagnostic and predictive single gene and genetic panel tests provide concrete, actionable insights that lead to informed decision making and personalized treatment.

ProGx Panels offer you the flexibility of panel testing with the diagnostic accuracy of the whole genome. Select the gene content from one of our fixed panels or create your list of genes based on your patient’s clinical indications.