This Milestone is editorially independent, produced with financial support from a third party. About this content.
Since the publication of the first draft of the human genome in 2001, the development of new technologies and bioinformatics tools and the ever-sinking cost of sequencing have made it possible to now assemble virtually complete and gap-free genomes and to precisely map different types of genetic variation in tens of thousands of individuals for genetic insights into population histories and diseases. This webcast brings together sequencing experts to discuss where the field is headed, sharing their perspectives on the future of human genome sequencing.