Vrije Universiteit Brussels

Apr 11, 2024 | academic.oup.com | Vrije Universiteit Brussels |Hôpital Erasme

Whole exome sequencing (WES) has emerged as a powerful tool for genetic research, enabling the collection of a tremendous amount of data about human genetic variation. However, properly identifying which variants are causative of a genetic disease remains an important challenge, often due to the number of variants that need to be screened.