Whole Genome Sequencing

Whole genome sequencing is the most powerful genetic test currently available to evaluate the health of a pregnancy. It is 2-3 times more likely to identify a meaningful genetic condition impacting pregnancy and fetal health as compared to the current standard of care, and results from genome sequencing inform and impact pregnancy and delivery management.

At the Women’s Genetics Center, whole genome sequencing test results are interpreted and analyzed by an expert team of laboratory geneticists at the New York Genome Center. Laboratory directors work closely with clinicians to ensure all patients receive timely and accurate results, with the understanding that genetic results can have an important impact on medical decisions.

Results from whole genome sequencing help patients and providers to understand anticipated pregnancy outcomes and recurrence risks. Currently, we are the only center to report on genetic conditions known to impact pregnancy, delivery, and postpartum health.