Microsoft Internet Explorer 402 Document NotSpecified7.8 lb. Normal0 recently published in Science, Daniel J., Professor of Genetics, University of Pennsylvania, Perelman School of Medicine. Dr. Rader and the Philadelphia Veterans Medical Center Scott M. Damrauer, an assistant professor, expressed great interest in the human genetic sequencing to improve human health.
Two experts commented on two important research findings related to human genetic sequencing published in Science. The former is a patient with a specific disease phenotype often has a certain genetic defect. The latter is likely to have a specific disease phenotype (eg, familial hypercholesterolemia) in people with specific genetic defects.
The story originated from the fact that Geisinger Health Systems recruited more than 50,000 people to sequence exons, which indicates that the prologue of genetic testing and precision medicine may be opened. As the genetic testing technology becomes more mature, the results are more accurate, and the price is cheaper, human beings have the magic weapon to detect the causes and effects of the disease. Genetic testing can be used to prevent problems before they occur, to remind people of high-risk groups to prevent in advance; it can also be used to determine the prognosis of disease; it can also be used to find new targeted therapeutic drugs and explore the efficacy of drugs. Scott M. Damrauer, very optimistic about the application prospects of genetic testing in clinical treatment, he even made a rhetoric in science: genetic testing technology will promote a new round of innovation in clinical treatment.
Of course, professors have their own reasons. Various diseases (such as diabetes/kidney disease) are related to genetic susceptibility or genetic variation. As ordinary people, we certainly hope that we will not get sick, but we also hope that the scientific elite will step up research and strive to crack the relationship between human gene sequences and diseases at an early date.
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