Your complete genome.
From €500.
We sequence 100% of your DNA using cutting-edge NGS technology and analyze it with artificial intelligence. Actionable results for you and your doctor.
WGS 30x sequencing · Interactive GenePortal report · Lifetime updates
It’s that simple
From your doorstep to your results, in 4 weeks.
Order your kit
Receive everything you need for sample collection at home.
Collect your sample
Saliva or blood, depending on the test. Step-by-step instructions included.
We sequence your DNA
Cutting-edge DNBSEQ technology + validated bioinformatics pipeline.
Receive your results
Interactive report on GenePortal + clinical PDF for your doctor.
Solutions for every need
Whether you want to explore your own genome or you’re a researcher with an ambitious project.
For your health
- 🏭 Complete genome + GenePortal — from €500
- ☤️ Genetic diagnosis (clinical exome) — from €300
- 👶 Fertility test (carrier screening) — from €200
- 💊 Pharmacogenomics · Polygenic risk · Ancestry · Nutrigenetics
For research
- 🧬 WGS 30x — from €500 (volume discounts)
- 🎓 WES 100x — from €300
- 🔀 RNA-seq — from €200/sample
- 🖥 Standalone bioinformatics · Targeted panels · Metagenomics
Not all genetic tests are created equal
Most tests on the market read less than 0.1% of your DNA. We read 100%.
| OmicaLabs (WGS) | Typical SNP chips | |
|---|---|---|
| Genome coverage | 100% | < 0.1% |
| Variants analyzed | > 5,000,000 | ~700,000 |
| Rare / private variants | Yes | No |
| Structural variants | Yes | No |
| Full pharmacogenomics | Yes (clinical PGx) | Partial |
| Reanalysis with new discoveries | Yes, for life | No |
| Clinical utility (diagnosis) | Yes (ACMG/AMP) | No |
What our clients say
I got my complete genome out of curiosity and ended up discovering I’m a slow metabolizer for several medications. My GP adjusted a prescription I’d been taking for years. The difference has been enormous.
We’ve had 40 samples sequenced with them this year. Data quality is excellent and turnaround is always on schedule. For a small research group, having a nearby, accessible lab makes all the difference.
The GenePortal report is the most comprehensive tool I’ve seen for explaining genomic results to a patient. The PRS scores with percentiles and pharmacogenomic recommendations save me hours of work.
Clinical case: diagnosis after 3 years without answers
A 34-year-old patient referred by her neurologist after recurrent episodes of muscle weakness and chronic fatigue. Neurology and myopathy panels from other centers had come back negative.
Whole genome sequencing at OmicaLabs identified a pathogenic variant in RYR1 (c.7300G>A, p.Gly2434Arg) classified as Pathogenic (ACMG: PS3+PM2+PP3+PP5). The variant was not covered by the previous panels.
The diagnosis enabled targeted follow-up and family genetic counseling, including testing for her two children.
Discover what your DNA says about you
Complete genome, interactive report, and lifetime updates. All from €500.
Order your test →