What Is Genetic Testing?
Genetic testing is a type of medical test that identifies changes in the DNA sequence, which we can pass on to our children. These changes in our DNA, called “pathogenic variants,” can manifest in disease. Genetic tests can detect such variants and confirm a disease diagnosis.
DNA is the genetic material in our cells that serves as the blueprint for our unique features. It carries the instructions that enable our body to perform various functions. Several different methods exist to quickly and reliably test our DNA; sequencing and deletion/duplication analysis are the most common. Biochemical/multiomic testing can often also aid in diagnosing disease earlier and can enable continuous therapy monitoring, especially in lysosomal storage disorders (LSD).
Going Beyond Genetics With Centogene Solutions.
Just as every disease is different, so is every patient. By taking a multidimensional approach, you are able to look at each patient from different angles to combine deep knowledge and insights for a holistic view. A multiomic approach addresses the various “omics” – Phenomics, Genomics, Transcriptomics, Epigenomics, Proteomics, and Metabolomics. This ultimately gives us a more complete picture of the underlying biology and what is causing the symptoms of any particular rare or neurodegenerative disease. This enables us to diagnose diseases quickly and with the highest accuracy possible – saving resources and sparing patients pivotal years during which a disease can rapidly progress. A quick definitive diagnosis can direct physicians to the treatments of today and the precision medicine of tomorrow.
By choosing our services, you gain access to a wide range of cutting-edge genetic and multiomic testing options. we understand that a timely and accurate diagnosis is crucial for patients and physicians, that’s why we offer a comprehensive diagnostic solutions in global clinical network, and deep medical expertise as powered by our International Partner Centogene GmbH, Germany.