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Screen time?
Open Forum | November 23, 2021Genomics England has announced a pilot programme of whole genome sequencing to screen for genetic diseases in 200,000 healthy seeming newborns, so should every newborn baby have their whole genome sequenced as a matter of course?
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Solving the genomic jigsaw puzzle of health
Open Forum | January 24, 2020A DNA database of thousands of healthy older Australians is set to change how we determine which genes may underpin a range of chronic and acute diseases.
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New database enhances genomics research collaboration
Open Forum | November 6, 2019Sharing datasets that reveal the function of genomic variants in health and disease has become easier with the launch of a new, open-source database developed by Australian and North American researchers.
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Bringing the power of genomics to patients
Clara Gaff | April 11, 2019Associate Professor Clara Gaff explains her life long interest in genetics and the potential for genomic testing to unlock exciting new treatments in the future.