Understanding your genetic susceptibility to certain medical conditions, and how to lower your level of risk through healthy lifestyle choices, can help prevent diseases from manifesting later in life.
Whole Genome Sequencing is a test that’s used to identify genetic variations within your DNA. The purpose of genome sequencing is to get vital medical information to ensure you can best take care of yourself.
Whole Exome Sequencing 100x
Build your customized plate depending on how your body handles food categories like carbohydrates, fats, dairy, and more to improve your health.
When it comes to food and nutrition, there is no such thing as a one-size-fits-all solution. That’s why we provide an in-depth range of tailored diet insights to help uncover your unique nutrigenetic profile.
What does the Nutrigenteic report analyze?
Whole Exome Sequencing 100x
Our DNA test helps you identify what your body needs to perform at its
peak, as well as how to avoid injuries that may hinder your performance,
and much more.
This is your personal genomic fitness report, providing valuable genetic insights into your physical fitness.
Topics covered include exercise and heart rate, strength, recovery, balance, mobility, reflexes, agility, precision, injury risk, BMI, fat, muscle, metabolism, blood pressure, cholesterol, Insulin, and glucose. On top of that, also shown in the report are personality traits, including optimism, leadership, conscientiousness, extraversion, learning
Whole Exome Sequencing 100x
This report tells you how specific genetic variants in your DNA can affect your chances of developing certain health conditions. on top of that, it guides you on optimal ingredients and skincare treatments, creating a truly personalized genetic-driven skincare management plan.
We identify your skin’s natural strengths and weaknesses based on your genetic results to develop a recommendation tailored specifically to you. By understanding your genetic predisposition to wrinkles, cellulite, inflammation, and other skin conditions, you can make more informed choices to eliminate, and reduce visible signs of aging.
Whole Exome Sequencing 100x
Finding out early if you’re genetically at risk for certain health disorders might help you avoid them later in life.
When a family member has a trait for a disease it’s wise to have genetic testing and screening to find out if you are a carrier, or if you might have the disease yourself.
Some genetic variations can increase our risk of developing certain health conditions, other variations can reduce them, it’s recommended to find out your own personal genetic composition and where possible, reduce your risk through lifestyle changes and preventive measures.
Which Disease areas are included?
Cardiovascular, respiratory, gastrointestinal, renal, endocrine (hormonal), ears, eyes, musculoskeletal, dermatological, men’s health, women’s health, mental health, reproductive health and sleep health.
Whole Exome Sequencing 100x
This is your personal Pharmacogenomic Report containing a wealth of information about how your unique genes are likely to have you react to specific
medications. It indicates what drugs may or may not cause you to experience adverse reactions. Your report shows an analysis of huge amounts of
genomic data; associating genetic variants found in genomic files with variants known in scientific literature.
All of us respond differently to medications and this can be down to our own unique genetic make-ups. Because we are each so unique, a drug that might
be effective for one person can be ineffective for another.
The same goes for safety: a drug that could be safe for one person could be less safe for the next person.
Noninvasive Prenatal Test with Qiagen technology
NIPT is a quick and painless prenatal test that looks at DNA from your baby’s placenta to identify whether you’re at increased risk of giving birth to a child with a genetic abnormality.
NIPT screens for a variety of chromosomal disorders, including:
The test can also detect sex chromosomal disorders, like Jacob’s syndrome, Klinefelter’s syndrome, Trisomy X, and Turner’s syndrome.
Using a simple saliva sample, we can collect 100% of your DNA and analyze the genetic sequence.
The sequence is divided into several parts, amplified, grouped in clusters and then sequenced.
This sequencing process reveals the order of nucleotides that make up the original DNA sample.
We then compare the genome with a generic and globally recognized reference DNA sequence.
Yes. The genome test, based on the Whole Genome Sequencing process, is able to detect
susceptibility to specific genetic diseases. For a very focused analysis, we provide a special version of this
test that matches your genetic makeup with your clinical records.
Our Partner Lab has its own laboratory and proprietary software experience. This internal
infrastructure allows us to develop a very complete service to take care of your needs. We have different types of analysis to suit any level of depth and price.
No. Our mission is to democratize genetic data to allow people to make informed decisions about their health and wellness. With this goal, we want to develop reports and services that help you establish a prevention plan or develop a real personalized diet or training to take care of your body.
We are very glad that people can discover the power of genetics thanks to the curiosity to know more about their family roots, but we want to focus as much as possible on that science that improves people’s health for a long and happy life.
It takes approximately 4-8 weeks for your reports to be delivered to you, from the day we receive your sample in our partner’s lab.
