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)?
Report of genetic variants
Ready for diagnosis
Maximum coverage for carrier status (diseases that can be inherited by your children)
Possibility of genetic consultation (at additional cost)
Access to all your genomic files (VCF, BAM, FASTQ)
Decode ALL your DNA - Genetic information to your advantage
Personalized suggestions about your nutrition and sport
Predisposition to injury, disease and drug metabolism
Learn about your ancestry, genetic mix and genetic behavior.
Decoding the 100% of your DNA
Other tests only 0.02%
What products
we offer at ADNTRO?
HOME KIT
- 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?
HOME KIT
WGS (30x)
Other companies
Markers (SNPs)
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)
What does WGS give me access to?
Your entire genome will be available for life
EXPLORE MY GENOME
EXPLORES THE GENOME
ADNTRO'S FULL REPORT
ADNTRO'S FULL REPORT
VARIANT REPORT
CARRIER STATUS
CARRIER STATUS
READY FOR DIAGNOSIS
READY FOR DIAGNOSIS
GENETIC CONSULTATION*.
GENETIC CONSULTATION*.
EXPLORES 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 DIAGNOSIS
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 (at additional cost) to receive consultation and advice from our genetic and bioinformatics team to help with all the doubts 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?
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:
- FASTQ
- BAM and BAI
- VCF SNP
- VCF CNV
- VCF INDEL
- Others: XLS, PDF of reports, ...
- Bonus: Circus Plot
- Diagnostic report (contracted separately)
