Massive parallel sequencing technology has become the predominant technique for genetic diagnostics and research. Many genetic laboratories have wrestled with the challenges of setting up genetic testing workflows based on a completely new technology. The learning curve we went through as a laboratory was accompanied by growing pains while we gained new knowledge and expertise. Here we discuss some important mistakes that have been made in our laboratory through 10 years of clinical exome sequencing but that have given us important new insights on how to adapt our working methods. We provide these examples and the lessons that we learned to help other laboratories avoid to make the same mistakes.
Keywords: NGS data analysis; clinical exome; clinical variant interpretation; genetic diagnostics; next generation sequencing; whole exome sequencing.
© 2022 The Authors. Human Mutation published by Wiley Periodicals LLC.