National legislation is required to protect people against life insurance discrimination based on their genetic results.

A suite of best-practice tools developed by GeneEQUAL will support health professionals to provide inclusive, person-centred and respectful genetic health care for people with intellectual disability.

The ethical issues surrounding genomic testing are often complex and varied. A Question of Ethics is a four-part blog series by Australian Genomics, in collaboration with the Biomedical Ethics Research Group at the Murdoch Children’s Research Institute.

Front Line Genomics interviewed Felicity Boardman, Professor of Social Science in Genomics at Warwick University in the UK, who aims to bring lived experience perspectives to reproductive genetic technology.

The involvement of community members in the actual process and design of health research would be much more prevalent if people were aware they could do it, an Australian Genomics…

In a world-first, Monash University is leading a DNA screening program that will allow Australians aged 18-40 to assess their risk of cancer and heart disease. It is thought that early detection of these diseases will allow young Australians to make more informed health decisions.

Queensland Genomics have produced a Genomics Information Toolkit for patients and families affected by rare disease. Information provided includes: what genomics is,
how it might help you or your family, where Queenslanders can get testing and the different kinds of genetic tests that are available.

Australian Genomics has released an animation of the genomic testing journey, taking the viewer through the different people and processes involved. This video was created as part of Australian Genomics’ First 5 Years celebrations.

Although genomic sequencing is a powerful tool, it isn’t always the most appropriate test. This article explains when genomic sequencing will be most useful, and the associated benefits and risks.