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Whole Genome Sequencing for 500 Euros: What You Get

Just ten years ago, sequencing a complete human genome cost over €10,000. Today, at OmicaLabs, we offer a 30x whole genome with an interactive report for €500. How did we get here? And more importantly: what do you actually get for that price?

The Sequencing Cost Revolution

The Human Genome Project (1990–2003) cost $2.7 billion. Since then, sequencing costs have fallen faster than Moore’s Law: a factor of 100,000x in 20 years. Next-generation platforms such as DNBSEQ (the one we use at OmicaLabs) have been key to this reduction, with reagent costs significantly lower than previous platforms.

What Is Included in the €500?

Item Included
Sample collection kit Yes
Shipping logistics Yes
DNA extraction + quality control Yes
WGS 30x sequencing (PE150, DNBSEQ) Yes
Full bioinformatics analysis (BWA-MEM2, GATK, snpEff) Yes
Interactive GenePortal report (ancestry, traits, PRS, PGx…) Yes
Clinical PDF report for your physician Yes
Raw data (FASTQ, BAM, VCF) Yes, upon request
Lifetime updates (ClinVar, new PRS models) Yes

How We Compare to the Market

The leading European whole genome sequencing providers charge between €600 and €900 for a comparable service. SNP chip tests (which read only 0.1% of the genome) cost between €100 and €200, but lack clinical utility and cannot detect rare variants.

In summary: for the price of 3–4 private medical consultations, you get the most comprehensive genomic information available, with lifetime updates and real clinical utility.

Who Should Consider Whole Genome Sequencing?

Healthy Individuals with Curiosity and a Preventive Mindset

Whole genome sequencing is the most cost-effective long-term genomic investment. Unlike a panel or an exome, you are not limiting the analysis to what is known today: when new gene–disease associations are discovered, your data will be there to be reanalysed.

Patients with an Unresolved Clinical Suspicion

If targeted panels have not yielded a diagnosis, whole genome sequencing covers non-coding regions, structural variants, and repeat expansions that panels cannot reach.

Researchers

We offer volume discounts (>20 samples) and a standalone bioinformatics service. See our research pricing.

Ready to take the next step? Learn more about Your Personal Genome.

OmicaLabs