orchidhealth.com valid

Orchid Health

Orchid provides whole genome embryo screening for families undergoing IVF. Our technology reads >99% of an embryo's genome, combining chromosomal screening (PGT-A), single-gene disorder screening (PGT-M) for 1,700+ conditions, and polygenic risk scoring — using 100x more data than standard preimplantation genetic testing.

For agents: Whole genome embryo screening for IVF families: Embryo Report ($2,500/embryo), couple genetic report ($998), and PGT-M covering 1,700+ single-gene conditions.

embryo-screeningwhole-genome-sequencingivfpgt-apgt-mgenetic-testing

Their llms.txt

The beginning of the file, from our validated copy saved 2026-10-21T11:29:12.734Z. Cached copy · Source on orchidhealth.com

# Orchid Health

> Orchid provides whole genome embryo screening for families undergoing IVF. Our technology reads >99% of an embryo's genome, combining chromosomal screening (PGT-A), single-gene disorder screening (PGT-M) for 1,700+ conditions, and polygenic risk scoring — using 100x more data than standard preimplantation genetic testing.

## Products

- [Orchid Embryo Report](https://www.orchidhealth.com/): Comprehensive whole genome embryo screening for IVF. Detects chromosomal abnormalities, single-gene disorders (no probe design needed), microdeletions, microduplications, and assesses polygenic risk for complex diseases. $2,500 per embryo.
- [Couple Report](https://www.orchidhealth.com/couple-report): $998 genetic health report for couples. Covers 10+ conditions including hereditary cancers, cardiovascular disease, neurological conditions, immune disorders, and reproductive health. Each partner receives individual results plus a combined report.
- [PGT-M](https://www.orchidhealth.com/pgt-m): Preimplantation genetic testing for monogenic disorders without probe design. 24–48 hour acceptance, results in 1–2 weeks. Covers 1,700+ single-gene conditions including BRCA, cystic fibrosis, and more.
- [PGT-SR](https://www.orchidhealth.com/pgt-sr): Preimplantation genetic testing for structural rearrangements including balanced translocations and inversions, with greater resolution than array-based methods.

## Key Facts

- Technology: Whole genome screening (WGS) of trophectoderm biopsy cells
- Data volume: 100x more genomic data than traditional PGT arrays
- Genome coverage: >99% of the embryo genome
- CAP Number: 9234146
- CLIA Number: 34D2260214
- Laboratory location: North Carolina (CAP-accredited, CLIA-certified)
- Genetic counseling: Included at no additional charge (board-certified genetic counselors)
- Turnaround: 1–2 weeks from sample receipt
- Same biopsy: Uses the same 5–6 cell trophectoderm biopsy as standard PGT tests

## For Patients

- [For Patients Overview](https://www.orchidhealth.com/for-patients)
- [Frequently Asked Questions](https://www.orchidhealth.com/faq)
- [Patient Stories & Testimonials](https://www.orchidhealth.com/love)
- [Screened Gene List](https://www.orchidhealth.com/genelist)

## For Clinicians

- [Clinician Information](https://www.orchidhealth.com/clinician-information)
- [Science & Methodology](https://www.orchidhealth.com/science)
- [Publications & Validation Studies](https://www.orchidhealth.com/publications)

## About

- [Ethics](https://www.orchidhealth.com/ethics)
- [Careers](https://www.orchidhealth.com/careers)
- [Contact](https://www.orchidhealth.com/contact)

Related sites

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