What does your DNA say
about your health?
Find out what variants hidden in your DNA to take action. We decode the 100% of your DNA (Whole Genome Sequencing - WGS) and we guarantee your privacy.
Choose the more accurate genetic testing.
Are you looking for genotyping?
Why should I have a whole genome scan (WGS)?
Decoding the 100% of your DNA
Other tests only 0.02%
Whole Genome (30x)
Genotype (23andMe, AncestryDNA)
we offer at ADNTRO?
- Not valid for diagnosis
- More economical
- Genotyping: certain number of generally common SNPs
WHOLE GENOME SEQUENCING - WGS
- Valid for diagnosis
- Increased coverage
- Complete genome sequencing: all common and rare SNPs in your DNA
Why choose ADNTRO?
Number of genetic markers analyzed
3 billion (100% of DNA)
Valid for clinical diagnosis
High coverage and accuracy
Report with quality parameters
Genetic counseling with our genetic team (additional cost)
Possible dose adjustment with clinical validity
Diseases that can be inherited by your children
We do not sell your data to third parties
Access to ADNTRO report
We analyzed a large number of common traits and genetic predispositions.
The ADNTRO platform is alive. We update and include new reports periodically.
In addition to the interpretation of the results, we provide you with your files.
Sequence your genome
What does WGS give me access to?
Your entire genome will be available for life
They trust us
"The test that fully exploits the virtues of knowing our genetic code. It is the most complete and reliable test on the market"
Need a second opinion?
It all starts with a saliva sample
It's very simple! You can do it from home in less than 5 minutes.
Frequently asked questions
Genotyping (home kit) analyzes those variants in our genome that are polymorphic, i.e. that have a high variability between individuals and that are very frequent 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 to determine phenotypic variations in individuals.
Genotyping techniques analyze approximately 700,000 positions in our DNA. The whole genome analysis (WGS) analyzes your entire DNA. (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.
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 provide you with several formats so that you can explore your DNA:
- BAM and BAI
- VCF SNP
- VCF CNV
- VCF INDEL
- Others: XLS, PDF of reports, ...
- Bonus: Circus Plot
- Diagnostic report (contracted separately)