Tests
Genotyping, 40X whole genome, or your own data.
Choose per customer. Many partners sell genotyping as the entry product and 40X whole genome as the premium tier.
Entry
Genotyping + imputation
~750,000 markers measured, imputed to 200M+ variants. Powers wellness, nutrition and risk reports.
Premium
40X whole genome
Every base measured at 40X average coverage. Adds rare functional and rare medical variants, ACMG findings, advanced PGx, HLA, mitochondrial and family-planning reports, with the ACMG report included.
No kit
Bring your own data
Consumer files (23andMe, AncestryDNA), genotyping arrays, or whole genomes from any sequencing lab.
Whole genome
Why 40X matters
Coverage is how many times each base is read. More reads mean more confident calls, especially for rare variants.
| Low-pass (1–4X) | 30X (industry standard) | 40X (OmicsEdge) | |
|---|---|---|---|
| Reads per base | 1–4, most variants inferred | 30 on average | 40 on average |
| Rare variants | Not reliably detected | Detected | Detected with deeper coverage |
| ACMG findings | Not suitable | Supported | Included |
| Clinical PGx | Limited | Supported | Included |
Reports available with 40X whole genome
Functional Rare Variants
Disease- and Risk-Associated Variants
Loss-of-Function-Associated Variants
ACMG SF v3.3 Predisposition Report
Advanced Pharmacogenomics (PGx)
HLA & Antigen
Medical Disease Variants
Family Planning & Fertility
Mitochondrial
Whole Genome Genius Report
Plus every genotyping report, on more complete data
Reports
1,500+ reports, ready to white-label.
Sell individual reports, 50–60-report summaries by health area, or everything. Hide what you don't want to offer.
Wellness and lifestyle
Diet and nutrition, fitness, sleep, weight, skin, mood and cognition.
Disease risk
Polygenic risk for 1,400+ conditions, including 200 validated polygenic risk scores, compared with people of the same ancestry.
Clinical
Pharmacogenomics, carrier status and, with 40X whole genome, ACMG findings and rare variants.
Longevity and labs
Longevity reports, plus 4,000+ lab markers tracked alongside genetics.
See every report before you call
The full catalog, with what each report covers and which test it needs.
Don't see what you need? Tell us and we'll build it for you!
Beyond DNA
Two engines most genetics providers don't have.
Genetics shows what your customers are prone to. Our Lab Test Analyzer shows what is happening in their body now, and our Recommendations Engine tells them what to do about it.
Lab Test Analyzer
Reads blood-test results alongside each person's genetics, so a lab value is interpreted in the context of their genetic risk, and tracks it over time.
4,000+ lab biomarkers supported
Trends over time, with before-and-after for your programs
Interpreted alongside genetic risk, not in isolation
Recommendations Engine
Ranks 20,000+ diet, lifestyle and supplement interventions for each person, using their genetics, lab results, symptoms and goals, and maps them to your products or protocols.
Built from human trials, written by our scientists, not generated by AI
Mapped to your own catalog, products or protocols
Included in reports and available through the API
Customization
Make it yours, at every stage.
Launch with our defaults in days, or tailor each step as you grow.
01
Kits
Generic kits with no minimum, custom-branded boxes, or your own packaging.
02
Brand
Your logo, colors and domain on the platform, app, PDFs and emails.
03
Report selection
Choose exactly which reports your customers see, and how they are bundled.
04
Custom reports
Reports built to your spec and owned by you.
05
Custom recommendations
Diet, lifestyle and supplement advice mapped to your own products or protocols.
06
Language and region
Spanish and German ready to use, other languages by translation. Data hosted in the US or EU.
Your brand
One platform, every screen your customer uses.
Launch on our branded platform, build on the API, or add AI and a mobile app under your name.
Branded platform: a full SelfDecode clone under your domain
HyperIntelligence mobile app
White-label genome-aware AI LLM, by iframe or MCP
Delivery
Reach customers however you work.
No build
Branded platform
A full clone of the SelfDecode platform under your name and domain. Priced by scope.
Most popular
Developer-ready API
REST API with webhooks and a full sandbox. JSON, white-label PDFs, raw and imputed data.
Available now
White-label AI LLM
Embed our genome-aware AI LLM in your app with an iframe, or connect your own AI to each user's results through MCP.
Available now
HyperIntelligence mobile app
Our mobile app, under your brand, for customers to explore results on the go.
Logistics
Kits, lab and shipping, all handled.
Kits ship within 1 business day of an order
Prepaid return label in the US
CLIA-certified, CAP-accredited US lab for the US, Mexico and Canada
ISO-certified EU lab for Europe and beyond
Kit registration in your flow or ours, unbranded
Genotyping results in ≤10 business days from lab receipt
Launch in as little as 24 hours.
Basic API integration. 30 minutes with us gets you pricing and a demo account.