Genome editing and gene therapy

New technologies for genome editing and gene therapy have placed control of our own genetic code within the reach of humankind. With new tools it becomes possible to cure genetic diseases, to live healthier, longer, and happier lives, and to enhance human capabilities. How can we accomplish this? And what should we as a species do with these new abilities?

During the genome editing and gene therapy seminar we covered the experiments and inventions that led to the development of these remarkable new tools and technologies. These inventions were derived from life itself: isolated from natural organisms and adapted for scientific and therapeutic goals. We learned the history of how genome engineering tools, including CRISPR, and delivery technology, including AAV capsids, were created in their modern form.

We explored the ways in which genome editing and gene therapy technologies are giving individuals control over their own genomes, focusing on the treatment of genetic diseases. We described major companies and emerging trends in the gene therapy industry. We also discussed how and where new discoveries, including accelerated algorithms for genetic engineering, will lead us in the near and distant future.