Whole-genome embryo screening · IVF
The most comprehensive genetic test available for IVF embryos.
Orchid is the only lab using whole-genome sequencing on embryo biopsies, detecting disease risks standard PGT-A consistently misses.
Whole-genome screening
>99%
Traditional embryo screening
<1%
Coverage of an embryo's genome · Source: Orchid validation studies
1,700+ conditions in one cycle
Clinically validated technology
Same biopsy as traditional PGT-A
As seen in
The big idea
More data. Better answers.
Most embryo tests look at less than 1% of the genome. Orchid sequences more than 99%. That's a meaningful difference, even without the technical details.
Orchid · Whole genome
Covers far more conditions
Standard PGT-A
Chromosomes only
At a glance.
Four things to know about embryo genetic testing, before you go deeper.
It's done during IVF.
Uses the standard embryo biopsy: a few cells from the outside of each embryo, sent to the lab.
Screens for what matters most.
Genetic forms of neurodevelopmental conditions, hereditary cancer syndromes, and birth defects.
Results ready in 4 weeks.
Same turnaround as standard PGT testing. No added wait time for your cycle.
Genetic counseling included.
Complimentary sessions with a genetic counselor, before testing and after results.
U.S. couples · trying to conceive
Many will use IVF and face genetic-testing decisions.
Source: RESOLVE / CDC NSFGEmbryos with chromosomal abnormalities
In women 35+, the share rises sharply with age.
Source: ASRM 2024 PGT-A Committee OpinionConditions Orchid screens for
Across monogenic, structural, and polygenic risk.
Source: Orchid gene listThe four kinds
The four kinds of embryo tests.
Each looks for something different. Orchid combines all of them in a single whole-genome workflow.
Aneuploidy
Screens for an unexpected number of chromosomes such as Down syndrome, Trisomy 18, etc.
~1% of genome
Monogenic
Targets one known condition at a time (e.g. Cystic Fibrosis, Spinal Muscular Atrophy).
single gene per test
Structural
Detects translocations & large rearrangements.
structural-only
Whole genome
All four above + thousands of conditions + polygenic risk in one report.
>99% of genome
How it fits into your IVF cycle.
No extra cycle. No new clinic. Same biopsy that's already standard with PGT-A.
Pre-screen call
Complimentary 30-minute call with a genetic counselor.
Before cycle
Embryo biopsy
~5 cells per embryo.
During IVF
Sequencing
Orchid's CAP/CLIA lab.
4 weeks
Results review
Counselor walks you through.
Before transfer
Patient stories
Why families come to us.
Eventbrite co-founders Kevin and Julia Hartz chose Orchid's whole-genome screening to understand each embryo at depth before transfer. In journalist Ashlee Vance's Core Memory feature, Kevin explains why.
“Any way to mitigate those [diseases] is really a no-brainer.”
Kevin Hartz · Co-founder, Eventbrite
Kevin & Julia Hartz
Co-founders, Eventbrite · Orchid customers
“Orchid gave us clarity around the things that we care about, especially our family history of conditions. We move forward now with so much more confidence than we would have.”
Common questions.
Pulled from the actual questions our counselors hear most weeks.
The biopsy is performed on the placenta-side of the embryo on day 5 or 6 and has been used in IVF for over a decade. Studies show no measurable effect on pregnancy or live-birth rates.
Yes. Most clinics already do the same biopsy used for standard PGT-A, and Orchid uses that exact sample. No extra procedures, no workflow changes. We partner with fertility centers across the U.S. If your clinic isn't set up with Orchid yet, our team can help get them onboarded.
Standard PGT-A counts chromosomes (less than 1% of the genome). Orchid sequences over 99% of the genome, surfacing single-gene disorders, hereditary cancer variants, structural events, and polygenic risk in one report.
Orchid's Embryo Report is $2,500 per embryo.
Coverage varies by plan. We recommend checking directly with your insurance to confirm whether Orchid is covered.
That's exactly what the consult is for. A genetic counselor walks you through what each section covers, and you can opt out of any category you'd rather not receive. You're in full control of what's included in your report.
Talk it through with a counselor.
Free 30-minute consult. A genetic counselor walks you through your options and answers your specific questions. No pressure, no commitment to test.
Free · No obligation · HIPAA compliant