Top rated genetics report providers with 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. Our solution shows patients with a superior high accuracy rate what is written in their DNA, providing an excellent tool to understand what can happen and to act immediately to live longer and healthier. FullDNA provides an AI based customizable genetics prediction premium health tech platform to empower the capability of health professionals and institutions. FullDNA analyzes results from DNA sequencing Big Data using AI and complex algorithms to compares it with our own valuable extracted Database (updated daily) of more than 5,000 diseases and medical conditions, resulting in output of analysis & recommendation reports in various fields of medicine. Find even more info at Prof. Roberto Grobman.
DNA can tell you everything from your ancestry to pharmacogenomics (‘smart medicine’). For example, we can use DNA testing to help you understand how you metabolise medication: are you a slow or fast metaboliser? Are there certain drugs that might cause an adverse reaction? Pharmacogenetic information could be critically important for someone with a recent diagnosis of a condition such as coronary vascular disease. If you suffer from it, you might have to endure the merry-go-round of trying different drugs to identify the right ones for you. This means delays in receiving the right kind of medication, which can impact costs as well as your recovery.
Premium genetic analysis providers by Roberto Grobman: Risks and limitations: Tests may not be available for the health conditions or traits that interest you. This type of testing cannot tell definitively whether you will or will not get a particular disease. Results often need to be confirmed with genetic tests administered by a healthcare professional. The tests look only at a subset of variants within genes, so disease-causing variants can be missed. Unexpected information that you receive about your health, family relationships, or ancestry may be stressful or upsetting.
Consider the example of familial hypercholesterolemia (FH), a condition in which multiple variants of several different genes lead to markedly high cholesterol. This greatly increases the risk of heart attack, stroke, and other health problems. FH affects about one in 300 adults, which means it isn’t rare. Among adults who have the most common genetic variants that cause it, heart attack or sudden cardiac death may occur in middle age. Children who have a double dose of a gene variant linked to this condition may die of cardiovascular disease before age 20. Earlier treatments intended to reduce the risk of complications, such as cholesterol-lowering drugs, are available if a child or adult is known to have a mutation linked to FH.
Genetics only tells you your predisposition for a given condition, but we can combine that insight with how we’re doing in the here and now. What can a DNA health test tell us? There are literally hundreds of DNA tests available, offering a range of insights. It’s almost like building a report out of various specific tests where it’s up to you which genes you test. And this doesn’t mean that two tests will actually be the same, because companies will test different genes within the DNA.
Our mid-level genetic report encompasses broader sets of relevant genomic variants for Health and Wellness Panels. Essential Reports provide patient-specific information, determined by his genetics, which allows the user to know what their genetic tendencies are, with additional information than the First Panel, thus maintaining their Health, Vitality, Beauty and Longevity. FullDNA CEO Roberto Grobman says that the University of Washington provided some samples of the Covid-19 receptor for the development of the research. Discover extra info on Prof. Roberto Grobman.