Upgrade your health.
For the rest of your life.
A Want to know which diseases you're at risk for in the future.
B Want to know which medications are less effective for you and need dosage adjustment.
C Enable your doctor to tailor your treatment according to your DNA.
1 On our website or at a collection point, you purchase a collection kit and take a saliva sample or drops of blood from your finger.
2 You submit the sample at a collection point or send it to us by courier (in preparation).
3 Usually within six weeks, you'll receive a completed medical report and recommendations.
4 Every additional year, you'll receive a medical report updated based on the latest scientific knowledge.
1 Risk assessment for 150+ genetic diseases.
2 Information about your ancestry through Y and mt haplogroup assessment.
As a medical facility, we maintain medical confidentiality and follow strict GDPR rules.
Our collection kits are registered with SÚKL and results are evaluated by our geneticists.
We store your health data anonymously in encrypted form, offline, and it is your property.
One analysis with annual membership.
Plan includes:
Three-year membership with advanced features.
Plan includes:
Some of our competition will claim they can advise you on health even though their tests don't have clinical validity or accuracy.
They essentially do tests illegally and mostly incorrectly. Find out if they are a healthcare facility and if their collection kits have IVD certification - they most likely won't.
Our healthcare facility is certified and has all necessary authorizations. The same applies to our collection kits.
Our results can be accepted by doctors and other healthcare professionals.
Find out from the competition whether they have clinical validity and registered collection kits.
Our competition usually sequences only a small part of DNA. Most often they sequence only 1% of DNA (for example, only exomes).
Our competition often doesn't even know on what devices the sequencing was performed and on what basis the disease was determined and evaluated, because they just forward samples to another country and take over results without deeper analysis.
We sequence the entire 100% of the genome, without using PCR and with 30x coverage. We process the finished sequences ourselves and evaluation is performed by our doctors.
Sequencing the entire genome is necessary to detect diseases that are caused by genetic mutations occurring outside of genes.
Avoiding PCR is important especially in diseases with low frequency, where PCR is a source of incorrect results.
30x coverage means that every letter of your genome is measured 30 times across the entire genome.
Find out from the competition how much of the genome they sequence and what coverage they have.
Our competition usually delivers a report that contains no conclusive information.
Sometimes they just write that some mutation is present on a certain gene, but they don't say at which position exactly or how many times that mutation was proven at that location (coverage) to rule out sequencing errors.
They are more like genetic horoscopes.
We don't deliver a report, but a medical report that contains all the necessary information for you, but also for doctors and healthcare professionals.
Find out from the competition whether their reports contain information about coverage at the mutation site.
Our competition usually delivers a report, recommends you to exercise, eat yogurt, and that's it.
Our service archives an electronic copy of your genome and allows you to receive regular medical reports without the need to repeat sampling.
Your DNA doesn't change, but scientific knowledge does, so it's possible to regularly discover new information about your health.
You will find here evaluation of risks for 150+ genetic diseases and information about your ancestry through Y and mt haplogroup assessment. Additional insights about your DNA are added continuously during your membership and at least once a year are sent to you in an updated medical report.
Yes, based on the ethical questionnaire that is part of the registration, you can choose whether you want to know your predispositions to currently incurable diseases or not. You can also choose not to learn that you are a carrier of disease risk to the next generation. You can learn more in the Ethics Board section and in the ethical code and in the passive ethical questions.
Read it carefully and then follow the recommendations that arise from it. Prevention is important, as well as your overall approach to health and lifestyle. If you are interested in additional information, you can contact our doctor, who can provide you with additional information and recommendations.
In any case, keep a cool head. In case of increased risk of occurrence of some disease, our geneticist will recommend further steps and take care of you.
DNA test uses whole genome sequencing (WGS). This revolutionary technology analyzes your entire DNA sequence (100%) with high analytical accuracy. Unlike traditional tests of most competing companies that focus only on certain parts of genes (0.1%), WGS reads every part of your genetic code - more than 3 billion DNA bases. The biggest advantage of WGS testing lies in the fact that with the development of genetic research, your complete genome data can be repeatedly analyzed without the need to repeatedly collect DNA. This means that we can regularly provide you with new insights with regard to scientific development, all without the need to collect a new sample.
You will only undergo collection once. According to the type of membership chosen, you will then receive a new medical report every year updated with new scientific findings and recommendations arising from them.
Sequencing of PCR-free libraries on the NovaSeq X Plus platform with 30x coverage
This is a maximally accurate sequencing method. Each part of your genome is sequenced multiple times, which minimizes the probability of errors and increases the accuracy of the analysis. Our goal is to achieve sequencing coverage such that each base is read an average of 30 times.
DNA tests have no age restrictions, but for ethical reasons we currently only test customers aged 18+.
The biological sample is destroyed after the analysis is completed. The electronic form of your DNA is archived if you have chosen a membership that includes archiving. Archived electronic DNA is automatically deleted after membership ends. Deletion of already archived electronic DNA can also be requested at any time. Electronic DNA is stored in anonymous encrypted form on offline storage and is your property.
Yes, just purchase our collection kit for DNA analysis and then inform the gifted person to properly register their sample on the Portal.
The sample must be submitted to the collection point or handed over to the shipping company no later than 48 hours after collection.
While collecting the sample will really take you a moment, analyzing it will take us a while.
The following factors affect the delivery time of results:
For data security, we have chosen the highest known standards to eliminate potential system, employee or company failures. After archiving, your electronic DNA and results are only in two places - in the DNA bank and on the DNA carrier. Both in the DNA bank and on the DNA carrier, your sample is only in encrypted form. The DNA bank and DNA carrier are in geographically different locations so that, for example, in case of fire, data can be restored.
You can find your results after logging into the Portal in the Results section.
Yes, tests can be purchased in bulk for the whole family. However, for ethical reasons, we do not recommend our service for persons under 18 years of age. An important step is to perform registration of the collection kit by each family member. Avoid mixing samples by signing the collection kit with the family member's name.
Instructions for collecting the sample can be found in the collection kit box, on the paper instructions for use of the collection kit and in the video guide in our customer portal.
You can submit the sample at the collection point even without prior registration on the Portal. However, without properly completed registration on the Portal, you will not receive your DNA analysis results/medical report. When submitting an unregistered sample to the collection point, we will ask you to enter your email address and in the subsequent email we will ask you to complete registration on the Portal. If you choose to send the sample via courier, it must first be properly registered on the Portal.
DNA meter collection point is a unique machine where you can pick up a collection kit for DNA testing and then submit your sample to it if you don't want to use our courier sample pickup service. The collection point ensures safe storage of the sample under suitable conditions before its analysis. You can find a list of our collection points here.
You can find our collection points here.
It's not usual, but it can happen. Don't worry, in such a case we will contact you, provide you with a new collection kit, and you will provide us with a new sample. The new collection kit is free.
Yes, it's entirely up to you. The results are your property and you will receive them in a format that can be further shared with family or doctor. You can share results online through the Portal or download them as a file from it. The results and recommendations provided by us serve informational and educational purposes. If you need DNA analysis for diagnostic purposes, always consult your doctor!
