Canberra Clinical Genomics is a joint venture between Canberra Health Services, the main health service provider in the state, and the Australian National University. A diagnostic genomic service that improves diagnosis of patients by providing clinicians with access to state-of-the-art whole exome sequencing (WES), their multidisciplinary team of 22 aims to provide clinicians with information about genomic variation and help find answers to complex genetic health conditions.

We have been trusted partners to Canberra for over 6 years now providing them with our market-leading iPassport system – to read the full case study please see below:

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