For patients
Your embryos have more to tell you.
Standard IVF testing counts an embryo's chromosomes. Reticular reads that same data more deeply — catching causes of pregnancy loss that chromosome testing misses, and inherited risk that impacts lifelong health.
No new biopsy sample — we use your embryo data from existing PGT-A results.
Standard testing today
Chromosome count
Reticular adds
Pregnancy-loss genes + Lifelong health risk
Beyond chromosomes
Not every loss is about chromosomes.
Most miscarriages trace back to an embryo having the wrong number of chromosomes — and standard testing catches those. But when chromosomally-normal embryos don't lead to an ongoing pregnancy, the cause can lie in single genes that chromosome testing was never built to find. Reticular screens 500+ genes tied to embryo viability and pregnancy loss, in every embryo.
couples with unexplained, recurrent pregnancy loss — where the lost embryos were chromosomally normal — were found to carry a single-gene cause.1
Every finding is backed by published research and reviewed with a genetic counselor before you see it.
Christina, CPO at Reticular and Licensed Genetic Counselor
New research points to specific pregnancy-loss genes.
These genes impact the earliest steps of development — cell division, genome activation, implantation. A few examples from the panel:
TUBB8
Helps organize the structures that guide early embryo cell division.
NLRP7
Helps regulate early embryo development and implantation.
PADI6
Supports embryonic cellular organization and genome activation.
Variants in genes like these have been linked to developmental arrest and a higher risk of pregnancy loss.
1 Genetic Variants in Recurrent Euploid Pregnancy Loss (medRxiv, 2025): a single-gene cause was identified in ~25% (30 of 118) of families with unexplained, chromosomally-normal recurrent pregnancy loss. A finding is not a diagnosis and doesn't predict whether a transfer will succeed.
Lifelong health
How one embryo's genome shapes a lifetime of health.
Most common conditions aren't caused by a single gene — they're shaped by tens of thousands of genetic differences. A polygenic score reads all of them at once and turns them into a single, calibrated estimate of how likely developing a condition is, relative to the general population.
What makes Reticular unique: existing methods leave valuable genetic signal unused. Reticular is closing the gap between how much genetics explains about disease risk and how much polygenic scores can actually predict.
50–90%
of common-disease risk is heritable — what genetics could explain
A fraction
is what the polygenic scores deployed today actually capture
Published
we share how every Reticular score performs against real outcomes
We report risk across 24+ conditions, in the areas where genetics is well-established and there's something you can do about it:
Pricing
Better information shouldn't cost five figures.
Other services can charge $10,000 or more. Reticular reanalyzes every embryo you have — across every cycle — for one flat fee, using the genetic data your clinic already created.
Flat fee · all embryos, all cycles
$1,000
No per-embryo pricing. 100% refundable until analysis begins.
Data privacy & deletion
Your genetic data stays yours.
Genetic information is personal. We keep access limited, move sequencing files securely, and let you request deletion of your Reticular account and associated genetic data.
How we protect and delete genetic dataData movement is secure
Sequencing files move through secure transfer methods and access-controlled storage.
Access is limited
Only the people and systems needed to provide, review, secure, or support your report can access your data.
Deletion requests
Verified requests remove Health Data from active systems within 30 days, subject to required retention.
Give your baby the best start.
IVF is already expensive, emotional, and full of uncertainty. We make it easier to get the most from the data you've worked so hard for.