Independent Reviews · Updated July 2026

Your Complete DNA.
Decoded and Compared.

Whole genome sequencing reads all 6.4 billion base pairs of your DNA. We independently review and compare every major provider so you can choose with confidence.

6.4B
Base Pairs Sequenced
30×
Clinical-Grade Coverage
200+
Health Reports

Most DNA Tests Read Less Than 1% of Your Genome

Consumer genotyping tests from companies like 23andMe analyze about 600,000 positions. Whole genome sequencing reads over 6 billion — capturing what standard tests miss entirely.

🧬

Complete Variant Detection

WGS captures coding regions, non-coding "dark matter" DNA, mitochondrial DNA, and structural variants that genotyping arrays completely miss — including variants linked to rare diseases.

FASTQ → BAM → VCF
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Clinical-Grade Accuracy

At 30× coverage, every position in your genome is read an average of 30 times. This redundancy pushes accuracy above 99.9%, meeting the threshold for physician-actionable medical reports.

Q30 ≥ 90%
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Future-Proof Your Data

Your genome doesn't change, but what science understands about it does — constantly. Full raw data means your results can be re-analyzed as new discoveries emerge, without re-testing.

Test once → Analyze forever

Side-by-Side: Every Major WGS Service

Pricing, data access, turnaround times, and what you actually get — based on our independent research and verified specifications.

Provider Price Coverage Raw Data Turnaround Ships Globally
SelfDecode
$97–$297/yr AI Imputation* Upload only Instant (upload) ✓ Online
Sequencing.com
$379+ 30× BAM + VCF 10–16 weeks ✓ Free
AncestryDNA
$99–$199 Genotyping only Limited export 6–8 weeks Select countries
23andMe
$79–$229 Genotyping only Limited export 3–5 weeks Select countries
FamilyTreeDNA
$79–$449 Genotyping / Y-DNA Limited 6–8 weeks

*SelfDecode uses AI-powered genetic imputation to predict up to 83 million variants from standard genotyping files, without requiring whole genome sequencing. Best used as an analysis layer alongside raw WGS data. Prices and features verified July 2026 and subject to change.

Sequence Your Entire Genome from €169

Dante Labs offers clinical-grade 30× whole genome sequencing with full raw data access — shipped free worldwide.

Get 10% Off with Code GENOME →
Use code GENOME at checkout · CLIA certified · 200+ reports

From Saliva to Sequenced in 4 Steps

No needles, no doctor visits. Here's what to expect after ordering.

Order Your Kit

Choose a provider, place your order, and receive a saliva collection kit at your door — typically within 7–10 days.

Collect Your Sample

Follow the included instructions to provide a saliva sample. Takes about two minutes. Seal and ship it back in the prepaid return mailer.

Lab Sequencing

Your DNA is extracted and run through an Illumina NovaSeq X sequencer. Every base pair is read an average of 30 times for clinical accuracy.

Reports & Raw Data

Access 200+ health reports online and download your complete raw data files (FASTQ, BAM, VCF) for use with third-party analysis tools.

Frequently Asked Questions

What's the difference between genotyping and whole genome sequencing?
Genotyping (used by 23andMe and AncestryDNA) reads about 600,000 specific positions in your DNA — less than 0.01% of your genome. Whole genome sequencing reads all 6.4 billion positions, including coding genes, non-coding regulatory regions, and mitochondrial DNA. WGS captures structural variants, rare mutations, and pharmacogenomic markers that genotyping completely misses.
What can I do with my raw genome data?
Raw data files (FASTQ, BAM, VCF) can be uploaded to third-party analysis tools like SelfDecode, Promethease, FoundMyFitness, and Sequencing.com's app marketplace. These tools provide additional health reports, pharmacogenomic insights, and trait analyses beyond what your sequencing provider includes. Your raw data is also valuable for future re-analysis as new genetic research is published.
Is whole genome sequencing safe? What about privacy?
The collection process is completely non-invasive — it's a saliva sample. Regarding data privacy, policies vary by provider. Look for companies that are HIPAA and GDPR compliant, don't sell individual data, and allow you to delete your data on request. We recommend reading each provider's privacy policy carefully before purchasing.
What does 30× coverage mean?
Coverage depth refers to how many times each position in your genome is read during sequencing. At 30×, every base pair is sequenced an average of 30 times. This redundancy dramatically reduces error rates — achieving Q30 scores above 90%, meaning at least 90% of bases are read with 99.9% accuracy. This is the standard threshold for clinical-grade results.
Can I use WGS results with my doctor?
Yes — providers like Dante Labs deliver CLIA-certified results with ACMG-classified variants, meaning they meet the standard for clinical use. Many genomic results can inform conversations with your physician about carrier status, pharmacogenomics (how you metabolize certain drugs), and hereditary risk factors. We always recommend discussing results with a qualified healthcare provider or genetic counselor.
Do these services ship internationally?
Dante Labs and Sequencing.com both offer free worldwide shipping. AncestryDNA and 23andMe are limited to select countries. SelfDecode is an online-only analysis platform — no kit shipment needed if you already have raw DNA data from another provider. Note that in France, submitting a DNA sample for recreational genealogy is technically prohibited under Article 226-28-1 of the French Penal Code.

From the Blog

Guides, comparisons, and the latest in consumer genomics.