In myGENetiks family we specialize in the management, diagnosis and consulting of hereditary diseases, orphan or rare diseases and counseling of high-risk pregnancies.
When no treatment works, it is essential to explore human genetics.

We refer our patients to specialist doctors for treatment and prevention, providing them with unique care. We are convinced that multidisciplinary treatment is the most effective and comprehensive treatment for patients. We integrate information and knowledge about genetic diseases, so that our patients make conscious decisions and actively participate in their treatments.

myGENetiks offers a line of “Personalized Medicine”, which takes our patient and their family by the hand, from their first interaction with us to providing the best treatment options available.

myGENetiks investigation provides services and consulting for biomedical and genome data. We provide specialized services to support the design of biological experiments and the analysis and interpretation of data. We also develop new technologies so that our clients obtain better results in less time. We use the experience of each of our professionals to ensure innovative and simple solutions.
Made by researchers for researchers, we specialize in:

• Genotyping and sequencing of samples
• Genomic data processing through our certified algorithms
• Consultancy in bioinformatics and genomic analysis
• Discovery of causal genes linked to a specific phenotype
• Design and construction of algorithms for the processing and analysis of genomic data
• Bioinformatics solutions and tools to run genomic analysis in the cloud

myGENetiks provides Next Generation Sequencing (NGS) and microarray services for all your needs.

Our scientific team has worked for over 10 years in the field of genetics, creating their own genetic analysis algorithms.

myGENetiks has successfully processed more than 18,000 samples using microarrays and 9,000 samples with exoma/genome sequencing data with different phenotypes: Autism, Mental Retardation, Microcephaly, Walker Burger, Beta Thalassemia, Congenital Sideroblastic Anemia, Centronuclear Myopathy and orphan diseases.

Through a saliva sample myGENetiks Kit offers our customers important information about their genome. In this process we use state-of-the-art technology that gives accurate results. Measurements are made by our team of researchers and scientists.
Our algorithm allows us to know the long racial lineage of our clients giving them in an understandable and animated way in our results page.

In addition, we have the ability to locate more than 100 traits or diseases, from an individual’s mathematical ability, muscle composition, tendency to certain emotions, marked personality traits to predisposition to kidney, neurological, cardiovascular, autoimmune or genetic diseases.

miGENetika-Kit uses the microchip called “Medicina Precisa” specialized for Latin America, with more than 900,000 markers that allow our clients to know their roots and genetic composition.