Genetic Sequencing

Are you and your partner seeking answers about the cause of your last pregnancy loss and wondering if there is a genetic cause?

We are seeking...

Couples who have experienced 2 or more clinical pregnancy losses AND at least one documented chromosomally normal pregnancy loss for which pregnancy tissue is available

Participants who have chromosomally normal pregnancy loss tissue available will be invited to undergo sequencing. The human genome is large and many changes in our genetic code do not cause disease, but other changes may explain a clinical problem such as miscarriage. Researchers will compare DNA sequences from mothers, fathers, and pregnancy losses to improve our understanding of novel genetic causes of miscarriage. 

Genetic trios composed of a mother, father, and past pregnancies will undergo whole genome sequencing and trio analysis. In some cases, where a genetic cause is suspected based on medical history, sequencing may be offered even if a complete trio is not available.  Living siblings, and additional family members, may provide DNA when available, as this may assist in determining the significance of unknown variants. In addition, couples will be asked to provide a hair sample, optionally, in order to assess for environmental toxins and stress hormones. Enrolled subjects may opt to receive actionable genetic variants that are identified in the trio analysis. Financial compensation is available for couples who are able to provide a complete trio of samples (mother-father-pregnancy loss).