Top genetic analysis services by Prof. Roberto Grobman: How we do it? We created a series of complex interconnected algorithms together with AI technology, capable of translating the scientific data and results of these scientific publications into useful information, and over the years we have been creating a unique FullDNA database. FullDNA has created a series of complex interconnected algorithms, capable of translating the scientific data and results of these scientific publications into useful information, and for over a decade accumulated a unique database.Today our database has more than 25 million publications and registered data and is updated daily with new publications and new research. Algorithmic platform for health data prediction based on genetic analysis. See extra information at Roberto Grobman.

With FullDNA DNA, we supply a series of reports that covers and sets out in a transparent manner: What genes we’re testing, why they’re important and what individuals can do about them. This last point is particularly important; we recommend real-world advice and guidance on how to make relevant lifestyle changes. All of this data might seem overwhelming, but we work with individuals to explain it and help them implement meaningful changes.

Genomic variants report companies with Prof. Roberto Grobman 2023: What are the benefits and risks of direct-to-consumer genetic testing? Direct-to-consumer genetic testing has both benefits and limitations, as they are somewhat different than those of genetic testing ordered by a healthcare provider. Benefits: Direct-to-consumer genetic testing promotes awareness of genetic diseases. It provides personalized information about your health, disease risk, and other traits. It may help you be more proactive about your health. It does not require approval from a healthcare provider or health insurance company.

Prenatal testing. For people planning pregnancy or who are already pregnant, genetic testing is available to check for an extensive number of conditions, such as cystic fibrosis and Down syndrome. Cancer. A number of genes are known to increase the risk of certain cancers. Testing may be especially important for people with a family history of these cancers. Perhaps the most well-known are BRCA mutations, which increase the risk of breast, ovarian, and several other types of cancer. People who don’t know their family’s medical history. For example, a person who is adopted and has no information about family medical problems may learn they are at increased risk of a preventable disease, such as heart disease or colon cancer.

Since the sequencing of the first genome, innovations have fuelled reduced sequencing times, which have in turn reduced costs. Today we are able to use that cutting-edge technology to understand how to use your DNA to live with the best possible health — to get the most out of your DNA and yourself. The road to DNA health testing: With anything that relates to clinical care, we always need sufficient evidence before we can ‘know’ something and make recommendations. In some cases, the research can take 10 years before there are proven outcomes, before it’s appropriate to bring to the general population or implement a large-scale deployment.

FullDNA Reports cover specific segments. To reach longevity, FullDNA’s Accurate Prediction Analysis is the most premium tool in the predictive genetics market for health professionals. Knowing in advance the susceptibilities for diseases and health conditions is different than analyzing mutations to find genetics diagnostics. We strongly believe reaching the future in a healthier way. Effective preventive measures can only be adopted when an accurate prediction methodology brings valuable ready to use data. Read extra info on Roberto Grobman CTO.