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About Us

Canberra Clinical Genomics (CCG) is an accredited medical genomic service in Australia's capital territory. We improve diagnosis of patients by providing clinicians with access to state-of-the-art whole genome sequencing (WGS) with clinically targeted genetic analysis . Our multidisciplinary team aims to provide clinicians with information about genomic variation and help find answers to genetic health conditions.

CCG is a partnership between Canberra Health Services (CHS) and the Australian National University (ANU), working together to diagnose patients with genetic disorders by sequencing their genome and potentially finding treatments that are personalised to their condition. WGS is performed at the ANU and funded for patients by CHS.

Our Vision and Role

In line with the rest of Canberra Health Services, our vision and role is our promise to each other and to you, our patients, and your family and carers.

     Vision: Creating exceptional health care together.

     Role: To be a health service that is trusted by our community.

Our Location

Our main lab is situated on Level 1 of the Australian Phenomics Facility (APF), our Sequencers are located next door at the Biomolecular Resource Facility (BRF) in the John Curtin School of Medical Research (JCSMR), and our Bioinformatics are processed through the National Computational Infrastructure (NCI), all three located at the Australian National University's (ANU) Acton Campus.

Address:

Canberra Clinical Genomics,
117 Garran Rd,
ACTON ACT 2601

Our Team

We're an experienced team and are able to provide the best case of personalised care. We're able to service our clinicians and patients as a name, not just a number. 

If you're interested in joining our team, you can send your expression of interest to ccg@act.gov.au or keep an eye out on the ACT Health Jobs page for upcoming employment opportunities at ACT Health and Canberra Health Services.

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