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

Decode ALL your genes and identify mutations
Get full access to your genomic big data

Determines an adequate diet and supplementation.

Find a suitable exercise plan for weight loss

Learn about the genetics of your mind, behavior and personality.

Use your genetic information to extend your life

Discover your oral microbiome

Find out how genomics research is applied to your test results

Decoding the 100% of your DNA

Other tests only 0.02%

Whole Genome (30x)


0 100%

Genotype (23andMe, AncestryDNA)


0 100%

DNATRO vs. other DNA tests

Other DNA tests2

Decode the 100% of your DNA.
Get the most comprehensive DNA testing enabled by whole genome sequencing.

They decode less than 0.02% of DNA.

Privacy First DNA Testing.
Access the technology that allows you to have full ownership and control over your genomic data.

They sell customers' genomic data.

New periodic reports.
You regularly receive new reports based on the latest scientific findings.

Reports are rarely updated.

Genome scanning tools.
Tools to browse your data, search for genetic variants and analyze genes.

No dynamic data exploration.

Deep genetic ancestry.
Discover your maternal and paternal ancestry with full mtDNA and Y-DNA sequencing.

Incomplete ancestry reports.

Access to Big Genomic Data.
All your genomic big data are available for download (BAM and VCF files).

There is no data or only limited data available.

Ready for diagnosis.
Take your data to your physician or genetic counselor for clinical interpretation.

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)

On Request
  • 🔹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).

saliva sample
steps DNA kit

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.


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.


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

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"The test that fully exploits the virtues of knowing our genetic code. It is the most complete and reliable test on the market"

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“…Innovative potential concentrated in the field of genetics”

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"ADNTRO seeks to promote the commercialization of its genetic detection kit"

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"Creators of a solution that allows us to decipher our genetic code at home."

Need a second opinion?

Cary sheremet
Cary sheremet
ADNTRO's very recent ancestry results…
Read More
ADNTRO's very recent ancestry results update are really outstanding, in my opinion ... READ MORE
Rúl Sanz
Rúl Sanz
The results are excellent
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The results are excellent, but what has surprised me the most are the personality traits. Impressive!
Ladi Oczelják
Ladi Oczelják
Amazing experience
Read More
Nice web, very good service and amazing adn information wow
Impressed with this new company!
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Impressed with this new company! They have been extremely helpful with all inquiries and respond very quickly to all questions. They continue to improve their site layout to make it more user friendly ...
Highly recommended
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A fantastic, fast service. Stunning results; very accurate over so many aspects of my own personality and health. Excellent, easily understood but thorough report.
Valentin Rivas
Valentin Rivas
Connecting the dots on yourself. 100% recommend
Read More
Impressed by the accuracy of several factors and excited to learn more about myself. Great design and solid science. Looking forward to further updates and new research! Keep the great work.

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:

  • BAM and BAI
  • 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)

spanish genome