STOREGENE
For Individuals
Take control of
your health
Whole genome analysis puts you in control of your health journey by offering personalised insights into your genetic health, disease risk, and potential responses to medications. Get a deeper understanding of your genetic makeup, and feel empowered to make informed decisions with your clinician about your lifestyle, preventive measures, and healthcare choices. Having a comprehensive view of your genetics can provide peace of mind, knowing that you’ve taken proactive steps to understand and manage your health.
What’s inside?
Whole Genome Sequencing
StoreGene’s comprehensive whole genome package represents a significant advancement in personalised medicine by bridging the gap between genetics and healthcare.
This package provides a powerful tool to deliver truly individualised treatment, ensuring individuals have the knowledge and support needed to take charge of their health.
Medication Optimisation
99.7% of the population carries a variant which could lead to an adverse drug reaction and yet medications are still prescribed to individuals on a one-size-fits all basis. By sequencing your genome your clinician can inform medication choices and dosages based on your genetic profile, reducing the risk of adverse drug reactions and improving treatment efficacy. For more information please visit our Pharmacogenomics page
An entire lifetime
of Genomics
Once you’ve had your whole genome sequenced, you have access to this wealth of genetic information for the life. This means, as the world’s understanding of genetics evolves, you won’t need to re-sequence to benefit from new discoveries. We can simply retest your existing data. To find out more about reasons to choose whole genome sequencing, visit our why whole genome page.
Health and Wellness Guidance
In addition to medical insights, we can also offer guidance on nutrition, fitness, and lifestyle choices that are personalised to your genetic makeup, helping you optimise your well-being. As with everything else, as new discoveries are made, we can test you without the need for re-sequencing.
