What does your DNA say about your health?
Do you suspect any genetic pathology?
Are you thinking about having children and you are concerned What diseases can they inherit?
Learn which pathogenic variants your DNA contains so that you can take action with the more accurate genetic testing. We decode the 100% of your DNA and guarantee your privacy.
Why have a complete genome done?
Use your information genetics in your favor
Ready for diagnosis
Maximum coverage for carrier status (diseases your children can inherit)
Decode ALL your DNA and know pathogenic mutations (diseases)
Get access to all your genomic archives (VCF, BAM, FASTQ)
Genetic consultation (at additional cost)
Learn about your ancestrygenetic mix and genetic personality ("with which you are born")
Personalized suggestions about your nutrition and sport
Predisposition to injuries, diseases and metabolization of drugs
Decoding the 100% of your DNA
Other tests only 0.02%
What is the difference between a genome
of other tests?
In the DNA there are regions that give rise to proteins (in charge of "executing the actions" of our organism) and regions that the regulate. These are the exons and introns, respectively.
Throughout the DNA there are common genetic variants (polymorphisms) that predispose us to suffer from certain pathologies or that determine our common traits. Our home kit analyzes these polymorphisms and allows to know the genetic predisposition you have to certain traits - Never diagnostic.
There are rare variants associated with pathologies that are not analyzed with the kit.
In case you want to know if you have exonic or intronic pathogenic variants is required perform a complete genome (WGS).
Why choose ADNTRO?
HOME KIT
WGS (30x)
Other
companies
Markers
Number of genetic markers analyzed
3 million
3 billion (100% of DNA)
700.000
Valid for clinical diagnosis
High coverage and accuracy
Report with quality parameters
Genetic consultation
Genetic counseling with our genetic team (additional cost)
Clinical pharmacogenetics
Possible dose adjustment with clinical validity
Carrier status
Diseases that can be inherited by your children
Privacy:
We do not sell your data to third parties
Access to ADNTRO report
We analyzed a large number of common traits and genetic predispositions.
Periodic updates
The ADNTRO platform is alive. We update and include new reports periodically.
Genetic assets
In addition to the interpretation of the results, we provide you with your files.
Raw
Raw
Sequence your genome
Whole Genome
- 🔹100% DNA sequencing.
- 🔹23,000 Genes
- 🔹Access to ADNTRO reports +1 year of updates
- 🔹Quality report
- 🔹File delivery detailed
- 🔹Ready for diagnosis (30x average coverage)
It all starts with a saliva sample
It's very simple! You can do it from home in less than 5 minutes.
What do we deliver with WGS?
Your entire genome will be available for life
Explore the genome
Download VCF, BAM and FastQ files with all genetic information, ready for variant analysis and variant prioritization in the clinical context.
ADNTRO'S FULL REPORT
Possibility to access to all ADNTRO report sections with the maximum precision and GWAS studies: health, pharmacogenetics, origins, nutrigenetics, sport, personality and labs.
Ready for diagnostics
Our whole genome sequencing data are of the highest quality. highest quality and can be used by physicians, clinical geneticists and genetic counselors in the clinical context.
GENETIC CONSULTATION
We offer the possibility (with an additional cost) to receive consultation and advice from our genetic and bioinformatics team to help with any questions about these results.
What they say about us
"The test that fully exploits the virtues of knowing our genetic code. It is the most complete and reliable test on the market"
“…Innovative potential concentrated in the field of genetics”
"ADNTRO seeks to promote the commercialization of its genetic detection kit"
"Creators of a solution that allows us to decipher our genetic code at home."
Need a second opinion?
Frequently asked questions
Genotyping analyzes those variants of our genome that are polymorphic, that is, they show great variability between people and are very common in general (> 1% in the population). Genetic association studies (GWAS) are fundamentally based on this type of analysis and help to determine our predisposition to different diseases as well as phenotypic variations in individuals.
Genotyping techniques analyze approximately 700,000 positions in our DNA; compared, whole genome analysis (WGS), in which all your DNA is analyzed (the three billion base pairs) and therefore allows the detection of rare variants in the population. These rare variants tend to have a high impact on the development of diseases and susceptibilities and responses to them. This is the most commonly used genetic research technique in the world.
Firstly, our Home Kit comes at a cheaper price.
With these microarray kits we perform genotyping, which reads approximately 700,000 positions of your DNA, which is sufficient for some common traits, but cannot be used for diagnosis or detection of rare variants.
First, we at ADNTRO send a kit to your home for collecting a DNA sample (a simple saliva sample, 2ml). The delivery to your home, as well as the return of the sample to the laboratory, is included in the price.
From the arrival at the laboratory of your test (approx. 5 business days in Europe), your results will be ready in 4 weeks.
You can access your results online, explore all sections of ADNTRO (including health and pharmacogenetics) and download files with your genetic information.
A genetic consultation with a professional team certified by the European Union in molecular genetics is available. As well as by the ADNTRO bioinformatics team. The consultation will be via email. You can query any doubts regarding your results and we will help you in every way necessary.
No clinical diagnosis is offered. For this, you should consult with your doctor
We will give you several formats so you can explore your DNA.
For the WGS High-Pass you will receive:
- FASTQ
- BAM and BAI
- VCF SNP
- VCF CNV
- VCF INDEL
- Others: XLS, PDF of reports, ...
- Bonus: Circus Plot
- Diagnostic report (contracted separately)
For the WGS Low-pass:
