[50] Genomic Medicine and Personalized Medicine Flashcards
What is Genomic Medicine?
The medical discipline that involves using genomic information about an individual for clinical care.
What is Personalized Medicine?
The tailoring of medical treatment to the individual characteristics of each patient.
How does Genomic Medicine contribute to Personalized Medicine?
By providing information about a person’s genetic makeup to guide decisions made in regard to the prevention, diagnosis, and treatment of disease.
What are the potential benefits of Personalized Medicine?
- Increased effectiveness of treatment
- Reduced side effects
- Prevention strategies tailored to individual risk
What is the Human Genome Project?
An international research project with the goal of determining the sequence of human DNA and identifying the genes that it contains.
How has the Human Genome Project contributed to Genomic Medicine?
It provided a reference sequence of the human genome and identified genes associated with various diseases, which are used in genomic medicine.
What is Genomic Sequencing?
The process of determining the complete DNA sequence of an organism’s genome at a single time.
How does Genomic Sequencing contribute to Personalized Medicine?
By identifying genetic variants in individuals, which can inform personalized treatment strategies.
What are Single Nucleotide Polymorphisms (SNPs)?
Variations at single positions in a DNA sequence among individuals.
How do SNPs contribute to Personalized Medicine?
Certain SNPs are associated with response to certain drugs or risk of disease, which can guide personalized medical decisions.
Define the term “Pharmacogenomics”.
The study of how genes affect a person’s response to drugs.
How does Pharmacogenomics contribute to Personalized Medicine?
By understanding how a person’s genetic make-up affects their response to drugs, it can guide the choice of drugs and doses for each individual.
What is a Genetic Marker?
A DNA sequence with a known physical location on a chromosome and associated with a particular gene or trait.
How can Genetic Markers contribute to Genomic Medicine?
Genetic markers can be used to identify genetic variants associated with diseases, which can inform diagnosis and treatment decisions in genomic medicine.
What is Genome-Wide Association Studies (GWAS)?
An observational study of a genome-wide set of genetic variants in different individuals to see if any variant is associated with a trait.