Reproductive health
Reproductive health genetic tests provide valuable insights into fertility, pregnancy, and potential inherited conditions, helping individuals and healthcare providers make informed family planning and care decisions.
Patients
Clinicians
Non-Invasive Prenatal Testing (NIPT)
Non-invasive prenatal testing (NIPT) is a safe blood test that screens for genetic conditions in a fetus, providing early, accurate information without risk to the pregnancy.
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Patients
Clinicians
Expanded Genetic Carrier Screening
Genetic carrier screening helps you make informed choices for you and your family.
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Patients
Clinicians
Genetic Carrier Screening
Genetic carrier screening helps you make informed choices for you and your family and now it’s bulk billed.
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Pharmacogenomics
Pharmacogenomics explores how your genes affect your response to medications, helping healthcare providers personalise treatments for better outcomes. Tailor medications based on your genetic makeup for safer, more effective care.
Patients
Clinicians
Pharmacogenomics (Personalised Medicine)
Pharmacogenomic (PGx) testing can help you get on the right medication at the right dose, the first time.
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Oncology
Oncology genetic tests help identify genetic mutations and biomarkers associated with various cancers, enabling personalised treatment plans and more targeted therapies for improved patient outcomes.
Patients
Clinicians
Hereditary Breast and Ovarian Cancer
Hereditary Breast and Ovarian Cancer (HBOC) is a genetic predisposition that significantly increases the risk of developing breast and ovarian cancers that is passed down through the family.
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Patients
Clinicians
Inherited colorectal cancer syndromes
Inherited colorectal cancer syndromes are linked to 5 - 10% of colorectal cancers through inherited genetic variants.
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