If a patient's entire genome were present in their medical record, how would one go about interpreting it clinically? Similarly, if we had an entire electronic health record database that included human genomes, how would a researcher go about finding new or novel genetic associations?
ANS. If a patient's entire genome were present in it's medical record then it would definitely make the informed choices about the medical treatment . It would also depict the complete details of kind of gene the patient is having. Personal genomics can be used to predict or confirm a genetic disease eg if a woman is carrying BRCA 1 gene that is breast cancer gene and this information can be used to take certain preventive measures earlier .
if we have an entire electronic health record database that include human genome then it is definitely going to help researcher for finding new genetic associations because it would tell how genetic variants influence the suscepitibility to certain chronic diseases , would certainly accelerate the research and discovery of drug targets and new biologic pathways.
Get Answers For Free
Most questions answered within 1 hours.