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Book An AppointmentMolecular genetics is a field of biology that studies the structure and functions of genes at a molecular level, and their influence in determining the overall makeup of an organism. Over the years, there has been a shift in biomedical research of the study of diseases linked to organs, and the definition of diseases based on molecules and cells.
New technology has made it possible to isolate and sequence genes, to study their function and how they contribute to disease. This has enabled scientists to get extensive knowledge on the characteristics of many diseases and their molecular and cell biology. This knowledge has had significant implications for the development of more precise diagnoses and therapeutic approaches for diseases. Through the tools of molecular biology, molecular genetics relate the change in the structure and sequence of human genes to changes in protein changes and, ultimately, to health and the development of the disease.
Molecular genetics is rarely used as the first test for a less severe case of diseases whenever an easy, functional test is available. With this next-generation technology, modern personalized medicine is expected to evolve rapidly.
Molecular genetic testing identifies a unique scope of indicators which are different from traditional clinical laboratory testing. Molecular genetics experiments usually involve a combination of different techniques to isolate and analyze DNA or RNA from a specific gene. The testing approaches used may vary depending on the reason for testing, which might be diagnostic testing or carrier screening.
The type of patient samples collected for molecular genetic testing may also differ. The testing technique also depends on the nature of the genetic makeup of the disease being studied, the purpose of the test, and the condition of the specimen. Specific regulatory testing considerations are another aspect of these tests.
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