[Cite as http://purl.org/au-research/grants/nhmrc/1113531]
Prof Kathryn North
Brief description The sequencing of the human genome brings the possibility of more accurate identification of the underlying basis of many diseases. This technology has moved so rapidly, however, that clinical access has been limited. In this application, a national alliance of clinicians, researchers, health economists and policymakers will evaluate the case for clinical genomics across inherited disease and cancer, determine how best to deliver this to the patient and train a capable workforce.
Funding Amount $AUD 25,856,254.62
Funding Scheme Targeted Calls
Preparing Australia for the Genomics Revolution