Why test with Akkure
We create Medical Digital Twins, along with the whole exome sequencing with in depth pharmacogenomics reporting, which is the examination of an individual’s DNA in order to predict how they will respond to certain medications.
Accessible from the comfort of your home
Your DNA kit is shipped directly to your door, via tracked registered post.
Your data is Secure
Your secure account is created following a verification of your identity. Only you can access your account using your unique identifier.
Convenient and not invasive
Simple, quick and easy to take, with a step by step guide to collecting your sample.
Tracked at every step
Your sample will arrive at our genetics lab via tracked registered post, you’ll be informed every step of the way.
State of the art Science
Our partner genetics lab is an authorized medical laboratory. Our services comply with the highest level of quality standards and are ISO 15189:2012 and ISO 17025:2017 certified.
Be in Control
You own your Medical Digital Twin. Your Akkure Soulbound Medical Digital Twin cannot be owned by anyone else.
Build you health asset Like No Other
Your Digital Twin unlocks your Akkure Dashboard where you will be able to connect your wearables, upload your lifestyle information and access precision medical services.
| Akkure Whole Exome sequencing and Preventative Screening | Other online DNA tests | ||
|---|---|---|---|
| Cancer gene testing | Captures mutations across all genes, reports in detail on 51 genes linked to various cancers | Typically only reports on a small number of mutations across 2 genes linked to breast cancer | |
| Medical laboratory ISO certified | Yes | No | |
| Suitable for research | Yes | Yes | |
| Suitable for clinical testing | Yes | No | |
| Avoids population bias | Yes | No | |
| Future proof - ability to report on harmful variants found in future research | Yes | No | |
| Overlay other panels to report on diseases | Yes | No | |
| In depth pharmagogenomics reporting | Yes | No | |
| Advice provided on appropriate action on finding potentially harmful mutations | Yes | No | |