Genetic testing can give you actionable insights to improve diagnosis, prognosis, and patient care We use whole exome sequencing (WES) test method to identify changes in patient’s DNA that are related to their health concerns or are causative. Whole Exome Sequencing uses the power of Next Generation High Throughput Sequencing to analyze the entire exome of an individual through one single test.
ExoSeq® suite screens around 20,000 genes giving you the opportunity to obtain a unifying diagnosis for patients presenting with heritable rare diseases and genetic conditions of de novo (spontaneous) occurrence.
