genomics service for routine clinical practice

Canberra Clinical Genomics (CCG) provides clinicians with access to state-of-the-art whole exome sequencing (WES) to improve diagnosis of their patients in routine clinical practice. CCG comprises a multidisciplinary team that aims to provide clinicians with information about genomic variation to help find answers to complex genetic health conditions.

Bringing decades of genomic research to mainstream healthcare

Genetics in Medicine