Immenso
Know yourself
know your stripes
At Stripe2Be we provide Whole Genome Sequencing (WGS), analyzing 100% of your DNA. It is the most comprehensive, detailed type of genetic test available.
We break down your WGS data into easy to understand reports which are all about your individual Stripes.
- Stripe2be WGS (2 Weeks) - €750,00
- Stripe2Be WGS (8 Weeks) - €500,00
Stripe2Be for Epilepsy
Stripe2Be for Mental and Behavioral Illness
Stripe2Be for Neurodegenerative Diseases
Stripe2Be for People Needs
It is believed that 30% of the epilepsies have a genetic factor.
Genes are hugely complex though. We each have up to 2 million “steps” in our DNA ladders, each of which are different in every one of our 20-25,000 genes. On top of that, we have a:
- Huge range of genotypes (referring to our genetic characteristics);
- Huge range of clinical phenotypes (referring to our observable, physical characteristics);
- Individual gene expressions;
- Complex models of inheritance;
- Epigenetic modifications;
- Environmental and lifestyle factors;
The Stripe2Be WGS analysis simplifies your genetic complexities. Your individual reports can lead to a much quicker diagnosis of a genetic epilepsy.
Lots of mental health conditions can be formed of several separate (but overlapping) health issues, with the causes being a mix of genetics, lifestyle, experiences, and more.
Your genetic variations can’t be used to diagnose you with psychiatric illnesses but they can help to improve your understanding of contributing factors.
This is why at Stripe2Be we combine your genetic data with your medical health records to identify correlations with any symptoms.
There’s a huge interest in how genetics influence neurodegenerative diseases such as Alzheimer’s, Parkinson’s, Spinal Muscular Atrophy (SMA), and Amyotrophic Lateral Sclerosis (ALS). Using your genetic data, we can help identify if genetic markers can reliably identify risk of developing these diseases.
We can all have a genetic predisposition to a neurodegenerative disorder, but that doesn’t necessarily mean that we will develop it. So, whilst you aren’t able to change your genes, you can make recommended lifestyle changes to prevent, reduce the risk, or delay the onset of a disorder.
We strictly follow the American College of Medical Genetics (ACMG) guidelines for the development of new reports. The ACMG is the only professionally-recognized international interdisciplinary professional organization of its kind and where organizations must adhere to extremely high standards for membership.
Take advantage from your stripes
Many people strive to end their diagnostic odysseys, which last on average: 7 years. People are likely to have had multiple inconclusive tests, procedures, and even surgeries, resulting in none or incorrect answers for children, adults and families.
Many people strive to end their diagnostic odysseys, which last on average: 7 years. People are likely to have had multiple inconclusive tests, procedures, and even surgeries, resulting in none or incorrect answers for children, adults and families.
S2B democratizes genomic data and makes it simpler to achieve crucial information in the shortest time possible. But it is not enough and the S2B is bigger than you think: we will help you to be in contact with specialist geneticists for counselling, or a community of people with similar situations where feel free to talk about yourself and your life without barriers or tabù.
Many people strive to end their diagnostic odysseys, which last on average: 7 years. People are likely to have had multiple inconclusive tests, procedures, and even surgeries, resulting in none or incorrect answers for children, adults and families.
Increase the diagnosis canche
Empower yourself and your research for a diagnosis with genomics data and start to live a stripe-on-you life!
Empower the people you love and your research for a diagnosis with genomics data and start to live a healthier stripe-on-you life!
Don’t be afraid of a diagnosis, empower yourself knowing and taking advantage of your stripes!
Empower your work and your impact on the lives of people affected by rare disease!
You know how it is difficult for people affected with rare diseases to trust a method or a diagnosis, and to find someone to talk directly about the disease and its individual symptoms. We know it too. Being part of the S2B world means having a chance to obtain information about you, to get specific genetic counseling, and to access a community where you feel free.
The rare disease is only One stripe. Sure, it can affect many aspects of your lifestyle, but you can manage several of these by taking care of your nutrition, mental health, and physical fitness.
The rare disease is only One stripe, sure it affects many aspects of the lifestyle, but it is possible to manage several sides by taking care about nutrition, therapy, and fitness of the people you love.
The rare disease is only One stripe, sure it affects many aspects of a person's lifestyle, but it is possible to manage several sides by taking care about nutrition, therapy, and fitness of the people you love.
The rare disease is only One stripe, sure it affects many aspects of the lifestyle, but you can help your patient or friends by guiding and improving their nutrition, therapies, and physical activity.
Empower your work and your impact on the lives of people affected by rare disease!
Empower yourself and your research for a diagnosis with genomics data and start to live a stripe-on-you life!
What you get
Rare Disease Report
Using proprietary A.I. algorithms, our report aims at providing diagnoses for rare diseases from genomics data, reducing the time needed for filtering and prioritizing variants.
Pharmacogenomics
Learn whether you have specific genetic variants that may influence how your body processes over 120 medications. Build a personalized treatment plan with the most complete Pharmacogenomic Report on the market.
All Pathogenic Variants
Whether your journey has just begun or it started years ago, you may still not be sure what the real causes of your disease are, which is why we offer a complete variant analysis panel where to find the answers you didn't know needed to be asked.
Full Raw Data
Your genome does not change from birth on, but science does. For this reason the Whole Genome Sequencing Test is the best lifetime investment: sequence once, get actionable tools for life! Raw data formats available: FASTQ, BAM and VCF.
How it works
Three. Small. Steps. That’s all it takes in order to receive your own four unique WGS reports. You’ll have your WGS results - but then, there’s more! We have genetic counsellors for you to share your thoughts and feelings concerning your WGS.
Order & receive your Stripe2be test
Activate your test & provide your sample
