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
Decode ALL your DNA and know pathogenic mutations (diseases)
Get access to all your genomic archives (VCF, BAM, FASTQ)
Learn about your ancestrygenetic mix and genetic personality ("with which you are born")
Personalized suggestions about your nutrition and sport
Decoding the 100% of your DNA
Other tests only 0.02%
Whole Genome (30x)
Genotype (23andMe, AncestryDNA)
What is the difference between a genome
of other tests?
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
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
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?
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:
- 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: