Personalised healthcare starts with DNA testing.
We collaborate with leading genetics experts and internationally accredited laboratories to deliver medical-grade genetic tests and personalised clinical care straight to your doorstep so you can make empowered health choices for you and your family.
The science behind our tests
Twenty years ago, it cost $2.7 billion to sequence the human genome. Now, the price is closer to $1,000.
We use next-generation sequencing (NGS) - a modern technology used to read human DNA code much faster and cheaper than older methods — reading millions of small pieces of DNA at once.
This has made it easier to understand the link between our genetics and health. We can now use it to identify variations in genes that could lead to a disease so we can prevent health issues before they happen.
How your DNA becomes a report
When it comes to our DNA, human beings are 99.3% the same. That 0.7% is what makes each one of us unique. These differences are called variants.
Variants can be linked to certain health conditions or other traits.
Our internationally certified labs extract DNA from cells in your saliva sample. Then our lab processes the DNA and reads millions of variants in your genome.
Your genetic data is then analysed, and we generate your personalised reports.
Compare genetic tests
Explore genetic testing options tailored to your needs.
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| Reproductive risk |
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| Individual carrier result |
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| Medicare rebate |
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| Genetic counselling support |
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| Express return shipping |
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