Genetic Analysis Ultra (WGS 30x)

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€329,99
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€329,99
Regular price
Tax included. Free shipping

Get your Ultra (WGS -30x) genetic analysis, UL, and discover what your whole genome can tell you: more than 625 reports on your health, medications, traits, wellbeing and origins.

This product sequences your whole genome and complements the information from our other analyses. Whilst our genotyping analyses measure 750 000 markers and estimate 13 million variants through imputation, Ultra sequences your whole genome at an average coverage of 30x: each position is read around 30 times. This also detects rare variants that are difficult to capture with a chip. Sequencing also captures other types of variants, such as copy number variants (CNVs), large insertions and deletions, tandem repeats and rearrangements, whose interpretation we plan to incorporate into future updates.

What does the Ultra DNA Kit (WGS 30x) analyse?

Genetic analysis of your health

Your genetic susceptibility to more than 100 health conditions, whether you are a carrier of up to 282 hereditary conditions (compared with 102 in Advanced), and your genetic compatibility with more than 100 medications, including reports exclusive to Ultra.

Genetic Personal Traits

More than 90 personal traits, such as how light your eyes are, skin pigmentation, sleep duration, cognitive ability, blood clotting, the light-induced sneeze reflex or your height, among many others. Includes seven genes exclusive to Ultra, such as APOE or CYP1A2.

Wellbeing, sport and nutrition

Genetic Wellness Analysis: in nutrition, your genetic tendencies relating to lactose intolerance, vitamin and cholesterol levels, predisposition to coeliac disease or response to caffeine. In sport, performance and muscle regeneration, tendinopathies, body mass index and much more.

DNA Connect

Find relatives worldwide with whom you share DNA, up to fourth cousins, and connect with them if you both wish.

Ancestry DNA Test

Discover how your ancestry is distributed across 93 reference populations, your haplogroups (maternal and paternal lineages) and your percentage of Neanderthal DNA.

tellmeGen+ subscription

Get 3 months of tellmeGen+ FREE with your purchase! Make the most of your DNA sequencing: DNA Connect updates, new reports ready to unlock and access to the platform's new features.

Why buy the Ultra Genetic Analysis (WGS 30x) from tellmeGen?

  • You will discover more than 600 aspects of yourself: your health, medication compatibility, wellbeing, traits and ancestors, and you will be able to contact your genetic relatives. All from sequencing your whole genome.
  • You will have information about your genetic susceptibility to discuss check-ups, prevention and habits with your healthcare professional.
  • You will learn how your genes may influence the dosage, efficacy and adverse reactions of more than 100 medications: lifelong information to share with your doctor. Never change a medication on your own.
  • Your account is updated with new results and features. The first 3 months of tellmeGen+ are free; afterwards, you can keep your reports up to date with an annual subscription for just €29.99 (or the equivalent in your currency).
  • Guidance on your results: tellmeGen's team of doctors and geneticists helps you interpret your results. You can also purchase nutrigenetic and pharmacogenetic advisory services, a report on variants of uncertain significance or a bespoke genetic report.
  • We process your genetic data in accordance with the General Data Protection Regulation, using encryption and technical and organisational security measures.
  • You can download your raw data up to three times a year at no additional cost.
  • Healthcare quality: tellmeGen is the brand of GENELINK, an authorised healthcare centre. We analyse your sample in European laboratories with certified quality systems, and our software is under evaluation by BSI to obtain CE-IVD marking.

Your genetic analysis pack will contain:

  • Instructions, accessed via the QR code, so you know which steps to follow at every stage. And if you have any questions, our team is here to help!
  • Oral sample collection kit: painless and easy to use in the comfort of your home. Rub the inside of each cheek with a swab: a RapiDri swab stored in a drying bag or, depending on the kit, two swabs stored in a tube with preservative liquid.
  • A large envelope and a transparent bag to return your sample to the laboratory, with free shipping.
Free shipping. Receive your kit in 2-4 days
Detailed information about your DNA
Immediate support for any questions
Secure payment

Only a cheek swab sample

Discover what whole genome sequencing can tell you about yourself, with a sample you take yourself comfortably from home.

Constant Updates

With the tellmeGen+ subscription, your reports on health, pharmacogenetics, wellness, personal traits, and ancestry are updated as genetic research advances.

Reports Divided into 7 Sections

More than 625 genetic reports on your health, medications, wellness, traits, and origins, plus DNA Connect.

Customer Service 7 Days a Week

Your satisfaction is essential. Our Customer Service team assists you Monday to Friday, 24 hours a day, and Saturdays and Sundays from 9:30 to 21:30 (Berlin time, CET).

Your genetic analysis kit includes

1. Instructions 2. Cheek swab sample kit 3. Bag for safe sample return

Follow these simple steps

1. Purchase 2. Register it 3. Collect the sample 4. Send it back at no cost 5. Receive your results

Constant updates

tellmeGen+ offers you updates to your reports for only €/USD 29.99 per year (or the equivalent in your local currency). The first 3 months of service are on us!

Reliability and privacy

Each sample goes through automatic quality controls: if it does not reach 20x coverage, the result is withheld and reviewed by our team. In addition, we comply with the General Data Protection Regulation.

Technology and laboratory

We sequence your entire genome with an average coverage of 30x, with each position read about 30 times, and we interpret single-nucleotide variants (SNVs) as well as small insertions and deletions, including rare variants. Sequencing also detects CNVs, large insertions and deletions, tandem repeats, and rearrangements; we plan to incorporate their interpretation in future updates.

Hundreds of health reports at your disposal

Almost 500 reports on genetic vulnerability, hereditary conditions, and pharmacogenetics, within the more than 625 Ultra reports.

Inherited conditions

More than 280 hereditary conditions: find out if you are a carrier of variants you could pass on to your children, from metabolic conditions to cardiac, ocular, or hereditary cancers.

Populations, Haplogroups and Neanderthal DNA

Discover how your ancestry is distributed among 93 populations, your haplogroups, and your percentage of Neanderthal DNA.

Get to know yourself better and take care of yourself

Discover more than 90 personal traits and your genetic tendency in nutrition and sports, to take care of yourself with more information.

Discover new genetic relatives

Find people with whom you share DNA and communicate with them.
FAQs

Frequently Asked Questions

We tell you how we work: tellmeGen is the brand of GENELINK, an authorized health center in Spain, and the interpretation of your data is done by our team of geneticists, bioinformaticians, and medical doctors. We analyze your sample in European laboratories, our software is under evaluation by BSI for CE-IVD marking, and, with Ultra, you receive more than 600 reports, updates with tellmeGen+, and DNA Connect.

626 reports: 107 on genetic vulnerability to health conditions, 282 hereditary conditions, 102 pharmacogenetics, 91 personal traits, and 44 wellness reports, in addition to your ancestry (93 populations, haplogroups, and Neanderthal DNA) and DNA Connect.

Register your kit, take the sample by rubbing the inside of your cheeks with the swab, and send it back with the return envelope, at no cost. You will have your results in your private area between 4 and 6 weeks after the laboratory receives your sample. In Spain, before shipping, a doctor evaluates the prescription of the test.

Your results are only seen by you in your private area. We treat your genetic data in accordance with the General Data Protection Regulation and do not share them with third parties without your explicit consent. Check the details in our privacy policy.

We sequence your genome with an average coverage of 30x: each position is read about 30 times, which gives solidity to each reading. Each sample goes through automatic quality controls, and if it does not reach 20x coverage, the result is withheld and reviewed by our team. Results with health implications must be confirmed with a clinical test before making decisions.

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