Integrate genetics into your practice
Personalize professional advice, integrate genetics and differentiate yourself from your competitors.
Integrate genetics into your practice
Start from scratch and become an expert
Your complete genetic solution
With your own brand
Customized for your practice.
You have the control
You own the results and therefore the relationship with your patients.
A single analysis for life
DNA does not change, in fact it allows a lifelong follow up of your patients for life, saving time and testing.
Easy to interpret and with personalized recommendations
You don't need to be an expert. It allows you to easily validate your clinical suspicions and integrate genetics into your consultations.
Training and support
It includes training and support by professionals, so you can get the most out of the tool.
Integrating genetics into your practice has never been so easy.
Receive kits
of saliva collection
Send them to our laboratory for analysis
Explore the results on our platform
Make personalized recommendations
Manage your
database
A solution tailored to your needs
NUTRITION & FITNESS
Specially designed for nutrition and fitness clinics. Indeed, it offers information on nutrigenomics: intolerances, efficacy of different diets, vitamins and minerals, digestive pathologies, muscle fibers and more information that allows you to personalize your recommendations. In short, this resource is an essential tool for any nutrition clinic or fitness center looking to provide a personalized service based on the individual's genetics.
DERMA
Designed for dermatology clinics. It offers information on skin properties and aging. It also provides details on skin and hair supplements, as well as pharmacogenetics in dermatology, including anti-alopecia treatments, allowing you to integrate genetics into your dermatological consultations.
CARDIO
NEURO
Focused on psychiatry clinics and psychological offices, this solution provides information on nervous system diseases, mental illnesses, behavioral disorders and genetic behavioral traits based on Robert Plomin's studies. By using this solution, psychiatry and psychology professionals can access genetic knowledge that allows them to better understand the causes and risk factors of various mental conditions. This can also aid in the diagnosis, treatment and personalization of care to improve the quality of life of patients.
PHARMA
Report providing information on predisposition to adverse effects and the need for dose adjustments for more than 150 drugs, supported by the research of the Stanford University (PharmCAT) and the FDA. By using this report, physicians can take into account their patients' genetic information to determine the appropriate dosage of a drug and avoid potential adverse reactions. Consequently, this allows for a more personalized and safer approach to drug treatment.
Included with 
Included with 
Comprehensive sample management
Saliva kits, logistics and access to the personalized platform for professionals, with online and pdf reports.
State-of-the-art genetic technology
Illumina Arrays and Whole Genome Sequencing
Periodic updates
Based on new scientific studies
Powered by AI
Help in interpreting results with AI
Genetic data management and privacy
Sample privacy is our top priority
Training and support
It includes training in the use of the tool by professionals to get the most out of it.
Examples of use cases
Harness the power of genetics and integrate it into your practice.
Trusted by
Scientific Support
The PRS (Polygenic Risk Score) is a measure that assesses the risk of developing a disease by taking into account multiple genetic variants associated with the disease. It also helps to predict the likelihood of developing certain diseases by considering the combined influence of several variants in different genes, providing a more complete picture of a person's genetic risk.
By using the PRS, healthcare professionals can identify individuals who have a higher genetic risk of developing certain diseases. In effect, this can aid in early prevention, diagnosis and the design of personalized treatment and management strategies.
Recent ADNTRO Research
provides its services worldwide
provides its services
around the world
We are present in more than 60 countries
USA
Mexico
Chile
Spain
UAE
Malaysia
Frequently Asked Questions
Do I need to be an expert in genetics to interpret the reports?
It is not necessary to have advanced knowledge in genetics. That is why the reports we provide are clear and easy to understand, including detailed interpretations of the results and practical recommendations to apply with your patients.
How do I collect samples from my patients?
We provide you with all the necessary material to collect samples from your patients. This material will allow you to send the samples to our laboratory,
where we will proceed with the DNA extraction and also the elaboration of the online report.
Are the results reliable?
The reliability of our reports is backed by scientific research, which is referenced in each report. This allows you to access studies that the results are based on and explore
the genetic markers identified in each sample.
Can this test be used as a diagnostic test?
The test based on a genotyping array is not diagnostic, but indicates genetic predispositions or protections. To obtain a valid diagnosis, it would be necessary to perform a Whole Genome analysis.
At all times we speak of genetic predisposition, that is, the increase or decrease in the probability of the appearance of a condition, a disease, or a certain behavior according to genetics, among other traits.
For example, it may be that genetic predisposition indicates that your patient tends to have lower than average levels of vitamin B9 or HDL cholesterol, but in a recent blood test the patient has high levels. This is because the environment and diet also influence these parameters and must be taken into account when making personalized recommendations for each moment.
Where do I send the samples and what technology do you use?
The kit we provide includes everything you need to send your samples to our laboratory. We use microarray technology for genotyping, specifically the Illumina "GSA array" chip, which is an advanced tool that allows detailed analysis of more than 700,000 genetic markers across the human genome. As a result, this technology allows us to obtain a comprehensive view of genetic variations such as SNPs (single nucleotide polymorphisms) and CNVs (copy number variations), which are fundamental for genomic studies, biomedical research and clinical applications. In addition, to provide a more complete understanding of your genome, we implement genetic imputation techniques, which allow us to estimate more than 3 million additional genetic markers. This methodology uses genomic reference databases and statistical algorithms to predict genetic variants that are not directly genotyped by the GSA chip, significantly expanding the scope of our genetic analysis. This holistic approach not only improves the accuracy of our genetic reports but also enriches the interpretation of genetic data, thus facilitating deeper discoveries about health, ancestry and personal traits.
Is it necessary to repeat the test after a few months?
It is not necessary to repeat the DNA test, since the DNA does not change. Therefore, you save your patients, since in only one test you have all the information. However,
we update the interpretation of the results as scientific research progresses, which may change some results over time, but you will be able to have
access as it is an online report.
