Online and in-clinic visits for genetic consultations, counselling and testing
Department of Cancer Genetics
Expert genetic guidance for couples navigating hereditary cancers, targeted treatments and genetic risk of cancers concerns — led by Dr. Roshan Daniel, Clinical Geneticist.
Genetic testing can tell you if cancer runs in your family, your risk of getting it, catch it early, and guide treatment down to the molecule
CANCER RISK ASSESSMENT
Hereditary cancer risk
Some cancers run in families. BRCA1/2 mutations, Lynch syndrome, and other hereditary syndromes significantly raise the risk of breast, ovarian, colorectal, and other cancers. Identifying these mutations allows at-risk individuals and families to take proactive steps — through surveillance and risk-reduction — before cancer develops.
TARGETED THERAPY AND PRECISION ONCOLOGY
Cancer treatment tailored to your tumor's DNA
No two cancers are genetically identical. Tumour genomic profiling analyses the DNA of your cancer to identify the specific mutations driving it — matching you to targeted therapies most likely to work for your tumour, and away from treatments unlikely to help.
EARLY DETECTION OF CANCERS
Multi-Cancer Early Detection (MCED) test like Grail Galleri test
MCED testing analyses a single blood sample for signals from multiple cancer types — often before symptoms appear. Designed for individuals who want to go beyond standard screening, particularly those with a family history of cancer. Early detection, when actionable, can be lifesaving.
CANCER PHARMACOGENOMICS
Choose the right cancer drugs and doses based on your genetics
Your genes influence how your body processes cancer drugs — affecting both efficacy and side effects. Pharmacogenomic testing allows your oncologist to personalise drug selection and dosing from the start, reducing toxicity and improving treatment outcomes.
