What does your DNA say about your health and ancestry?
Discover your roots and what runs in your family so you can take action, with the most accurate genetic test that decodes 100% of your DNA and guarantees your privacy.
What do you want to learn from whole genome sequencing?
Learn about your ancestry and find new relatives
Determines an adequate diet and supplementation.
Find a suitable exercise plan for weight loss
Use your genetic information to extend your life
Discover your oral microbiome
Decoding the 100% of your DNA
Other tests only 0.02%
DNATRO vs. other DNA tests
Other DNA tests2
Decode the 100% of your DNA.
They decode less than 0.02% of DNA.
Privacy First DNA Testing.
They sell customers' genomic data.
New periodic reports.
Reports are rarely updated.
Genome scanning tools.
No dynamic data exploration.
Deep genetic ancestry.
Incomplete ancestry reports.
Access to Big Genomic Data.
There is no data or only limited data available.
Ready for diagnosis.
Data unusable for diagnostic purposes.
Choose your genome sequencing package
Whole Genome (30x)
- 🔹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)
Whole Exome (150x)
- 🔹100% exome sequencing
- 🔹23,000 Genes - All variants of your genes.
- 🔹Possibility to study virtual gene windows (virtual gene panels).
- 🔹Detailed file delivery
- 🔹Quality report
-
🔹Ready for diagnosis (150x 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 does WES and WGS study include?
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 exome or whole genome sequencing data are of the 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.
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"
“…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, whereby approximately 700,000 positions of your DNA are read. This is sufficient for understanding some common traits, but it cannot be used for diagnosis or detection of rare variants.
Our own comparative studies between 4x and 30x show a quality level difference of over 90%. This applies particularly to differences in those regions and variants that are more difficult to detect - these can only be determined with 30x.
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
If you decide to have an exome or genome test, we will offer targeted analysis of variants detected in a specific subset of genes. You can contact us by filling out this contact form for more details.
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:
Differences between virtual panels, exome (WES) and whole genome (WGS)
