Next Generation Sequencing technology has been applied to clinical diagnoses in the past three
to five years using various approaches including target gene panels and whole exomes. The
purpose of this book is to summarize the experiences the results advantages and disadvantages
along with future development in the area of NGS-based molecular diagnosis. This up-to-date
volume will not only provide the readers working with Next Generation Sequencing the basics on
how to apply the technology to molecular diagnosis but will present the results and experience
of practical application.
