GeneSyte^™ prenatal genetic testing

Genea’s GeneSyte^™ prenatal genetic testing is a blood test that a pregnant woman can undertake in the first trimester of pregnancy, to look for chromosome errors that her baby may have. The most common known chromosome error is Down syndrome (Trisomy 21). For such an important test, you’ll want to have the best. It’s therefore important to know that GeneSyte^™:

• has the lowest “failure to report” rate of any pre-natal tests on the market
• results are provided 99.9% of the time^{^}
• we don’t just provide risk scores (like some tests do), we give a result – in other words, we give you an answer.

The reassurance of knowing with GeneSyte^™

Our exclusive screening test provides definitive answers on a wider range of chromosomal abnormalities during pregnancy.

How does GeneSyte^™ work?

During a woman’s pregnancy, some of the baby’s DNA crosses the placenta into the mother’s bloodstream. GeneSyte^™ is a prenatal test that involves taking a blood sample from the mother and testing for the baby’s DNA. Scientists look for changes in chromosome numbers, checking for conditions which are caused by extra or missing chromosomes. At Genea, we can test all chromosomes but some of the most commonly known diseases we test for are Down, Edwards and Patau syndromes. GeneSyte^™ can also report on the sex of a baby.

What is the difference between GeneSyte^™ and other tests on the market?

There are other products on the market that sound very similar but quite simply, they are not. The most important thing a patient wants to know is that if she has her blood collected, she will have a result. Some competitors have a 'failure to report' result 3-5% of the time. However, 99.9% of the time^{^} we provide a result. 

More about GeneSyte^™