The coronavirus pandemic brought the topic of genome  sequencing to homes as biotechnology quickly created mRNA vaccines for COVID-19.  Genome sequencing  is a laboratory method that is used to determine the entire genetic makeup of a specific organism or cell type. This method can be used to find changes in areas of the genome. These changes may help scientists understand how specific diseases, such as cancer, form. Results of genomic sequencing may also be used to diagnose and treat diseases. Genomics is a rapidly growing field that has revolutionized the way we understand biology. In this course topic, students will gain a comprehensive understanding of the sequencing, characterization, and study of DNA, and how it is possible to decode the complete genetic complement of any organism.

The content is designed to provide an integrative approach to genome science, incorporating the latest technologies and insights arising from genomic research. Students will learn about genome sequencing, annotation, and analysis using various types of genomic data and bioinformatics tools. 

At the end of this course, students will have a solid understanding of genomics and the latest genomic technologies that are transforming biology. They will also start to develop the critical skills necessary to review genomic data. With this knowledge and expertise, students will be well prepared for the future and have a competitive edge in the growing field of genomics.