The focus of the course is on clinical diagnostics using exome/genome sequences, variant identification and analysis including afternoon practical sessions. NGS technologies currently allow efficient sequencing of complete human genomes which have an enormous impact on diagnostic centres replacing many existing molecular and cytogenetic tests. More and more single gene sequencing is replaced by gene panel sequencing, whole exome sequencing (WES) and whole genome sequencing (WGS). This course aims to prepare all the community relevant to this field for innovations in molecular testing. There are VERY LIMITED NUMBER OF PLACES AVAILABLE!
Call for Abstracts. Submissions close 31 August 2018.
See the website for speakers and more details.