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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)
Genome bases are sequenced 30 times in average to ensure accuracy combined with Proprietary bioinformatics to identify all variants detected.
Cord Blood, Blood or Saliva samples, a Single essay for a full panel of analysis
Within 2 months a detailed report 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.
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.
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
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.