A NEW ERA OF MEDICINE IS HERE: WHOLE GENOME SEQUENCING

GenerationTM Whole Genome Sequencing is a diagnostic DNA testing service available for anyone in your family, including newborns. The test can identify many health problems before symptoms begin, such as inherited cancers, genetic disorders, and more. Sequencing your whole genome provides you and your physician critical insights enabling smarter health related decisions. Discover how you and your family can benefit from whole genome sequencing.

Whole genome sequencing is a process of mapping out the entire genome, which is all of the DNA in your cells. This process unlocks the genetic code and identifies mutations that signify predispositions to certain conditions. Knowing your, or your child's unique genetic DNA, can be a powerful tool for families to take a proactive approach to early detection, disease prevention and personalized medicine.

Why wait for symptoms to occur when you can take action now and plan ahead? Whole Genome Sequencing offers information far above and beyond what’s found in other DNA tests, allowing you and your physician to make smarter health related decisions by understanding the complete picture. Eliminate uncertainty around your family's health, and benefit from better outcomes, fewer negative reactions and personalized treatment plans.

Once your sample and completed paperwork arrives at our lab, DNA will be extracted from the sample and sequencing of the genome will be performed using next generation sequencing (NGS) technology. Pathogenic variants, known as mutations believed to be disease-causing will be presented to your ordering physician.

You can order your GenerationTM Whole Genome Sequencing test from the Generation Store. The diagnostic DNA test is available to anyone in your family, including newborns. If you have any questions, give us a call at 866-565-2237.

QUESTIONS? WE'RE HERE TO HELP.

To learn more, give us a call at 866-565-2237.