Canberra Clinical Genomics
Canberra Clinical Genomics (CCG) is a diagnostic genomic service in Australia's capital territory. We improve diagnosis of patients by providing clinicians with access to state-of-the-art whole exome sequencing (WES).
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Canberra Clinical Genomics (CCG) is a diagnostic 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). Our multidisciplinary team aims to provide clinicians with information about genomic variation and help find answers to complex genetic health conditions across all clinical specialties including, but not limited to: neurology, cardiology, renal, immunology, haematology, inherited oncology and congenital disorders.
CCG is a partnership between ANU and ACT Health, working together to sure patients with complex diseases by sequencing their genome and finding treatments that are personalised to their condition. Whole Genome Sequencing is performed at ANU and funded for patients by ACT Health.
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Clinical Bioinformatician
Location
Hugh Ennor Building
117 Garran Road
Acton ACT 2601
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.