Genomic information is precious – to patients, doctors and researchers.

Research informed by genomic information is increasingly integral to improving the healthcare of current and future generations. Melbourne Genomics has found that more than 90% of Victoria’s patients choose to share their genomic information to assist medical research.

Patients, clinicians, medical scientists and researchers have told us that genomic information needs to be shared seamlessly but securely and ethically.

The Alliance is building a genomic information system that will support patient care and enable secure and ethical access to information by doctors, patients and researchers.  

As it is developed over time, this leading-edge system will enable:

  • Doctors to be able to order the right genomic test at the right time for their patient
  • Patients and doctors to get genomic sequencing results
  • Medical scientists to analyse genomic variants and decide which variants are significant to health
  • Medical researchers to securely access data that will drive future discoveries while protecting patients’ privacy and confidentiality

Our genomic information system, GenoVic, will advance disease prevention and better outcomes for patients - contributing to global knowledge and enhancing individual care.


We could talk genomics all day, but we’ll send you only what’s useful and interesting.

Melbourne Genomics acknowledges the Wurundjeri people of the Kulin Nation, on whose lands we work, and all First Nations peoples across Victoria. We pay respect to Elders past and present. We also acknowledge the First Nations health professionals, researchers and leaders who are shaping the future of genomic medicine.

© 2014–2022 Melbourne Genomics Health Alliance