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.
Ask first, then match the kit to the person. Plus gifts for family historians that need no test at all.
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 |
From $449 checked Oct 25, 2026 |
30× | FASTQ + BAM + VCF | 6–8 weeks | ✓ |
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. Dante Labs price and turnaround checked on dantelabs.com on October 25, 2026; other providers last verified July 2026. All prices change, so confirm at checkout.
No doctor visits. Here's what to expect after ordering.
Choose a provider, place your order, and receive a home collection kit at your door.
Follow the included instructions. Depending on the provider that means a saliva tube or, for Dante’s current kit, a finger-prick blood spot. 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.
Read your reports online (Dante includes 90+, more with its Premium plan) 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.
Serious drug reactions were estimated to rank among the top causes of US hospital deaths. Some depend on genes a test can read.
About 80% of children who develop a genetic disorder have no family history of it, per a Mayo Clinic genetic counselor.
The strongest genetic risk factor for Alzheimer's — and one of the most useful genes to actually know about.
Bankruptcy, new ownership, and 14 million genomes in limbo. What happened and what to do now.
Same cup of coffee. Same dose. Opposite health outcomes — based on one SNP in your genome.
AncestryDNA, 23andMe, FamilyTreeDNA, and whole genome sequencing — compared honestly.