This course will provide an introduction to the applications of bioinformatics in our everyday lives. We will begin by exploring the function of DNA and genes, the sequencing of the human genome, and the advancement of sequencing technology. We will understand how DNA mutations lead to genetic diseases, and further discuss the bioinformatic applications in personalized medicine and cancer treatment. We will also explore the diagnostic potential of liquid biopsy and noninvasive prenatal testing in detecting genetic mutations and diseases. In addition, we will discuss the role of biobanks and genome-wide association studies (GWAS) in identifying disease-causing genes, as well as the ethical and privacy issues surrounding genomic data. We will also examine how bioinformatic analyses can reveal family histories and the genetic diversity of human populations.
Throughout the course, we will watch films and engage in group discussions to enhance understanding of the course material.