Making genetics less confusing.

We are not just another expensive fertility lab with more opaque tests. Established in 2020 by scientists and fertility patients, Progenic Genomics seeks to integrate the latest science to inexpensively work on your behalf, and present results that are straightforward, valuable, and empowering to you!

Many people think that routine preimplantation genetic analyses consider each embryo’s entire genome. They do NOT. We do.

We combine existing parental genomes with PGT lab data (even noninvasive) to identify your embryos’ entire genome. We then analyze each embryo for expected health risks and integrate all of those risks into a single, comprehensible, score. Selecting the highest scoring embryo to implant first (rather than one at random) can add years of healthy life to each child born, and the benefits are inherited by their children as well. We continuously integrate new peer-reviewed studies into each analysis to bring you the most current scientific knowledge.

EmbryoScore benefits improve with the number of embryos you have, but is actionable with even two. Benefits of your choice are heritable by your children and grandchildren!

Of course, everything we generate is intelligible, traceable, and yours to keep. We limit prices by reusing sequence data you already have, and during our pilot, analysis can be free!

Our goal is not to extract huge profits from billionaires. We are hopeful parents, like you! Instead, we seek to make this analysis a low-cost and demographically sensitive, standard of care for all human reproduction.