Duo Ultra (WGS 30x)

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$629.99
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$629.99
Regular price
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Get the Ultra (WGS -30x) Duo genetic analysis, UL, in Duo format and discover what your whole genome can tell you: 626 reports each on your health, medications, traits, wellbeing and origins. If you are taking this step with another person, the Duo pack costs less than two Ultra tests bought separately: you save €29.99 (or the equivalent in your local currency), with the same whole-genome sequencing for each person.

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. You will receive two sequencing analyses, one for each person, each with their own account.

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

Genetic analysis of your health

Your genetic susceptibility to 107 health conditions, whether you are carriers 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.

With the Duo pack, you will receive the 2 kits together in the same order.

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

  • Each person will discover more than 625 aspects of themselves: health, medication compatibility, wellbeing, traits and ancestors, and will be able to contact their genetic relatives. All from sequencing the 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 accounts are 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 per test (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. Each person has their own account and their results are private.
  • Each person can download their 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 samples 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!
  • Two drying bags, each with a RapiDri swab, to collect the sample by rubbing the inside of each cheek. A painless process that is easy to carry out at home, for both adults and children, even babies! A minor’s test is registered by their father, mother or legal guardian, who receives the results.
  • Two large envelopes and a transparent bag to return the samples 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
100% secure payments

Just a Saliva Sample

Discover what the complete sequencing of your genome could say about you with just a saliva sample and comfortably from home.

Constant Updates

With the tellmeGen+ subscription, you'll get the latest in genetic research applied to your health, pharmacogenetics, wellness, personal traits, and ancestry.

Reports Divided into 7 Sections

We provide you with over 600 genetic reports related to your health, ancestry, wellness, and personal traits.

Customer Service 7 Days a Week

Your satisfaction is our top priority. Our Customer Service team is available to assist you immediately Monday through Friday, 24 hours a day, as well as Saturdays and Sundays from 9:30 AM to 9:30 PM (Berlin CET).

Your genetic analysis kit includes

1. Instructions 2. Saliva collection 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 constant updates to your reports for just 29.99 €/USD per test per year (or the equivalent in your local currency). The first 3 months of service are on us!

Maximum reliability

The reliability of our system is 99.99%. Additionally, we strictly comply with the European GDPR.

Technology and laboratory

We examine up to 3 billion variants, with 30x coverage based on US technology and patents, detecting SNPs, rare variants, and CNVs, among others.

Hundreds of health reports at your disposal

Get over 600 genetic reports related to your health, inherited conditions, and pharmacogenetics.

Inherited conditions

Discover dozens of detailed genetic reports on the presence or absence of an alteration in the DNA sequence of a single gene.

Populations, Haplogroups and Neanderthal DNA

Discover how your ancestry is distributed across populations and haplogroups, as well as your Neanderthal DNA.

Know yourself better and improve your life

Adapt your lifestyle, sport, and diet according to the results of your genetic analysis. Learn about dozens of genetic personal traits that make you different from other people.

Discover new genetic relatives

Find genetic matches with other people and communicate with them.
FAQs

Frequently Asked Questions

We offer a large number of reports in our genetic analysis, providing you with an extensive amount of data. Additionally, our results are continuously updated, ensuring you have access to the most recent information.

You will access over 600 reports on how genetics influence dozens of physical and personality traits, wellness data, and ancestry with haplogroups and Neanderthal DNA, health and pharmacogenetics data, as well as participate in DNA Connect and contact genetic relatives.

From a simple saliva sample and from the comfort of your home, we can offer you one of the most complete genetic analyses. The laboratory extracts the DNA, and the geneticists read and interpret the results.

The results are 100% confidential. Once you register, your data is converted into an encrypted code. Neither in the laboratory nor during the analysis is there access to personal data, which will not be shared without express consent.

We use the latest technology and leading U.S. patents in the industry, with 30x coverage, meaning each nucleotide is read an average of 30 times. In this way, we analyze up to 3 billion genetic variants, minimizing error and confirming the accuracy of the results.

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