Whole genome

Whole genome sequencing (WGS 30x)

Genotyping reads specific markers; whole genome sequencing reads your entire genome at 30x coverage. It's the highest level of detail, and it can be re-analyzed every time science advances.

€950, VAT included · Blood sample · Results in 5–8 weeks

ADNTRO saliva kit box

Who we work with and what backs us

What the whole genome includes

Your entire sequence, not a selection

Genotyping reads specific markers; whole genome sequencing reads your entire genome, and that can be re-analyzed every time science advances.

Your entire genome, at 30x

Your whole genetic sequence is sequenced, not a selection of markers.

Re-analyzable

The data doesn't expire: when science describes something new, it can be re-analyzed using what you already have.

How whole genome sequencing works

Order your whole genome

Bought online, as a one-time payment.

A blood sample is taken

The whole genome is sequenced from blood, not saliva like the at-home kit.

Get your reports, and the ones still to come

In 5–8 weeks you'll have your results in your private account, and your genome can be re-analyzed as science advances.

Whole genome sequencing at 30x
GeneAI

Talk to your DNA

GeneAI reads your results and explains them in plain language. Ask it anything, as many times as you need, until you get it.

Things people ask it

  • What does my DNA say about my sleep?
  • Should I train for strength or endurance?
  • Do I need more vitamin D than average?
  • Where does my Italian ancestry come from?
Order your whole genome

Included with the Premium kit and the subscription.

Example conversation

  1. You

    Why doesn't afternoon coffee agree with me?

  2. GeneAI

    You have the slow version of the gene that metabolizes caffeine, so it can still be affecting you several hours after you drink it. Genetics explains part of it; sleep habits and routine explain another part that matters just as much.

    CYP1A2 rs762551 A/C High evidence
  3. You

    Explain it to me like I know nothing about genetics.

  4. GeneAI

    Your body takes longer than normal to switch off caffeine's effect. If you have it in the mid-afternoon, it's likely still working by the time you go to sleep.

GeneAI explains your results. It is not a medical diagnosis and does not replace consultation with a healthcare professional.

Maximum privacy and security

Your data is anonymous, and only you have access to it

We don't offer relative matching, in keeping with our principle of total sample anonymity.

Read the privacy policy
  • We don't sell or share your data

    We will never share or sell your data. When the chance to contribute to a scientific study comes up, we ask for your voluntary consent, and you can say no.

  • European servers

    Your data is processed on European Google Cloud infrastructure, under GDPR.

  • Your data is always yours

    You can download your data and delete all our records at any time, no explanation needed.

Seven areas, one sample

What does ADNTRO's genetic test offer?

ADNTRO's DNA test offers you more than 300 reports across seven categories: ancestry, nutrition, fitness, longevity, prevention, personality and fertility.

Ancestry

Which populations you come from and in what proportion, with your maternal and paternal haplogroups.

Nutrition

How you process lactose, gluten, caffeine, or fat, and which vitamins are harder for you to absorb.

Fitness

Whether your profile leans more toward strength or endurance, your recovery, and your injury risk.

Longevity

The genetic traits associated with aging and long-term health.

Prevention

Your predisposition to more than 300 diseases, with the study each one is based on.

Personality

Behavioral traits with a described genetic basis: sleep, sensitivity, appetite.

Fertility

Hormonal health and conception through your genes.

Scientific standard

Are DNA tests reliable?

Yes, when they use validated technology. ADNTRO analyses ~700,000 markers with an Illumina GSA chip in an ISO 17025-certified laboratory (Eurofins, Denmark), and its risk models are published in peer-reviewed journals.

  • Variants with evidence described in peer-reviewed literature
  • Informational results, never a diagnosis
  • Genotyping in a certified European laboratory
  • Results linked to the study they're based on, its population and sample size
  • UK Biobank as our validation base
See our publications
Cover of the article "Type 1 diabetes risk with neural networks", published in Int. J. Mol. Sci. in 2026Cover of the article "Late-onset Alzheimer's and polygenic risk score", published in Genes in 2025
Peer-reviewed, open access articles: you can open them and check the method yourself.

What our customers say

Jessica H.

I love it. Very informative.

@roman_nfkrz Let's get into my DNA test, see what it's all about and learn some science!
MissR

Love the insights they provide to my health journey. Brilliant data points to better understand how to improve your healthcare. They always come up with new markers.

Debbie

Our results show info missing on other tests but validated by years of family tree research. Really helped pull it all more together.

@francescapsychology Understanding your background can help you understand yourself.
Tonio A.

I like the reports, very detailed.

@jaydonehistory Ready to discover what your DNA says about you?
April

My experience with them was great. An informative and upstanding company.

Frequently asked questions

What sample does the whole genome need?
A blood sample, not saliva: that's what makes it possible to sequence the entire genome with the quality needed. The at-home kit, on the other hand, works with saliva.
How long does the whole genome take?
Between 5 and 8 weeks from when we receive your sample. That's longer than the saliva kit because the entire genome is sequenced, not a selection of markers.
Is it worth it compared to the saliva kit?
It depends on what you're looking for. The kit analyzes more than 700,000 markers and covers the same areas; the whole genome reads your entire sequence, so it can be re-analyzed whenever science describes something new, without taking another sample.
Who can see my data?
Only you. We don't ask for personal data when you register the kit, so not even we can link a sample to a person.
Do I have to pay for a subscription?
Not to access your reports. The subscription gives you access to updates and features like GeneAI; the first three months are free, and after that it costs €25 a year.
Is this a medical diagnosis?
No. Results are for research and educational purposes, and they don't replace consultation with a healthcare professional. We calculate your predisposition from published genetic association studies (GWAS), so you can explore your genetic code with context.

Your genetics are part of your story

Start there.

Order your whole genome
Order your whole genome