What is NGS Testing?
NGS testing, or Next Generation Sequencing, is a type of genetic testing that allows for the study of a person's entire genome in a single experiment. It can be used to identify a variety of genetic conditions, including inherited disorders, gene mutations associated with cancer, and more. NGS testing is becoming increasingly popular as a tool for diagnosing and managing various health conditions.
When Should I Do NGS Testing?
The decision of when to do NGS testing should be made in consultation with your doctor. Generally speaking, NGS testing is most useful for people who have a family history of a genetic condition or who have been diagnosed with a condition that has a genetic basis. It is also often recommended for people who are at increased risk of developing a genetic condition due to their ethnicity or family history.
What Are the Benefits of NGS Testing?
The primary benefit of NGS testing is that it can provide a comprehensive picture of a person's genetic makeup, which can be used to diagnose and manage various health conditions. Additionally, it can be used to screen for genetic variants that may increase a person's risk of developing certain conditions, such as cancer or heart disease. Finally, NGS testing can provide valuable insight into a person's ancestry and give them a better understanding of their ethnic background.
