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.
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.
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.
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.
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.
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 |
|---|---|---|---|---|---|
Dante Labs Top Pick |
€169–€399 | 30× | FASTQ + BAM + VCF | 8–14 weeks | ✓ Free |
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.
No needles, no doctor visits. Here's what to expect after ordering.
Choose a provider, place your order, and receive a saliva collection kit at your door — typically within 7–10 days.
Follow the included instructions to provide a saliva sample. Takes about two minutes. Seal and ship it back in the prepaid return mailer.
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.
Access 200+ health reports online and download your complete raw data files (FASTQ, BAM, VCF) for use with third-party analysis tools.
Guides, comparisons, and the latest in consumer genomics.
A data-driven breakdown of what each testing approach captures — and what it misses.
Upload your FASTQ or VCF files to these tools for health, ancestry, and pharmacogenomic insights.
One reads 0.01% of your genome. The other reads 100%. Here's how the cost-per-insight stacks up.