FROM A SINGLE SAMPLE WE ANALYSE A COMPREHENSIVE INSIGHT OF YOU

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Discover the different features of Genome

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WHOLE GENOME SEQUENCING 30X
Predisposition Risk on Cancers
Most Comprehensive panel with 22 cancers: Bladder, Bone, Brain, Breast, Endocrine, Neural, Epithelial, Eye, Gastrointestinal, Gynecological, Head and Neck, Hematologic, Kidney, Liver, Lung, Mesothelium, Muscle, Nervous system, Pancreas, Prostate, Skin and Urinary tract cancers.
Single-gene Diseases analysis (6 000+ diseases)
All disease related coding genes with known associated phenotypes
Pharmacogenomics
Ancestry (free option)
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Genome BASIC
Single
EUR 850
Genome PREMIUM
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Complete

full sequencing – more than 6 000 diseases screened (cystic fibrosis, thalassemia, Myopathy, hemochromatosis) – Cancer Predisposition Large panel (Breast, ovarian, uterine, colorectal, gastric, pancreatic, melanoma, prostate, kidney, bladder, etc)

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Accurate

Genome bases are sequenced 30 times in average to ensure accuracy combined with Proprietary bioinformatics to identify all variants detected.

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Safe & Convenient

Cord Blood, Blood or Saliva samples, a Single essay for a full panel of analysis

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Fast

Within 2 months detailed reports established by a Geneticist is available

At Genoma Swiss Biotechnology our mission is to enable people to have a better knowledge about their own health and that of their baby by investing doctors and families with most relevant early actionable genetic information to take appropriate medical decisions.
Genome is our own exclusive new-generation genetic test, performed in Geneva’s laboratory, one of the largest genetic centers for clinical diagnostics in Europe.

More than 6 000 Single-gene Diseases Screened

A single gene disorder is caused by variations or mutations in the DNA sequence of a specific gene. A mutation in just one of these genes is responsible for a disease.

In about 1 out of every 100 births, Single-gene Diseases, also called Mendelian diseases, occur when a deleterious variation takes place in a specific gene.

More than 6000 single-gene disorders have been identified. They are listed in the Online Mendelian Inheritance in Man (OMIM) database.

The common single-gene diseases can be classified into 13 medical panels such as below:

Cancer Predisposition Risk:
Most Comprehensive panel with 22 cancers

Cancer is induced by deleterious mutations in specific genes that activate the cells to grow in an uncontrolled and abnormal manner with the potential to spread into other parts of the body.

The hereditary identified deleterious variations have been shown to be associated with a high risk of developing certain cancers. The most acknowledged cancer predisposition genes are screened. Those cover a comprehensive panel with 22 cancers: Bladder, Bone, Brain & Nervous system, Breast, Endocrine, Neural, Epithelial, Eye, Gastrointestinal, Gynecological, Head and neck, Hematologic, Kidney, Liver, Lung, Mesothelium Muscle, Pancreas, Skin, Urinary tract cancers.

Preventive measures can be set up for patients of a high-risk group. Preventive actions can save lifes.

Pharmacogenomics
Personalise Drug Efficiency

Individuals have specific abilities to metabolize drugs that affect their efficiency. More than 200 drugs will be analysed, commonly prescribed for these following conditions:

Asthma, Cardiac Arrhythmias, Clotting Disorders, Congestive Heart Failure, Depression/Anxiety, Diabetes, Epilepsy, Heartburn, Hepatitis C, HIV, Hypercholesterolemia, Hypertension, Hyperuricemia (Secondary to Chemotherapy), Immunosuppression, Inflammatory Bowel Disease, Malaria, Nausea/Vomiting, Pain, Schizophrenia, Smoking Cessation, Tuberculosis

Ancestry
What Kind of Mix are You ?

When learning from relatives or from historical documentation is not enough, your DNA can help.

All generation specificities mark your DNA that can be identify and interpreted. Specific variations and identified patterns can reveal deeper ethnic and families origins.

Only Three Steps away from Results

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Order

Choose your preferred solution below, click on the "BUY" button and let you guide by the flow.

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Consultation

Your healthcare provider will help you to fill-out the test requisition form and make sure that you have all the necessary information to sign up the informed consent.

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Collection & Shipment

You will find in your kit the help and necessary items to perform and ship the sample collection. The sample shipment is fast and entirely covered by Genoma.

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Results

You will receive the Results within 2 months.

What is DNA & What information can be extracted?

DNA is made of around 3 Billions bases ranged in a way to code for who you are. Variations that could occur in this organisation may have an impact in the phenotype (involving health or not).

Among those, 1%, called “ form “genes”: the specific alignment of the bases are translated in proteins having each a determined function allowing life.

The human genome is built by around 20,000-25,000 genes. This in single-gene diseases, a mutation in just one of these genes is responsible for disease.

Variation in the DNA are:

Inherited

Variants passed down from the parent’s genes.

Not-inherited

Variants occurring in the germ line, “de novo” mutations or caused by environmental factors.

A Variant that has a deleterious effect is called “mutation”.