WHOLE GENOME SEQUENCING
The complete picture of your genetic health.
Sequenced once. Analyzed for life. Choose how much to unlock today.
PREMIUM
$449
One-time payment. Not a subscription.
Hereditary risk screening
Medication processing (pharmacogenomics)
200+ clinical reports
AI genome chat
RECOMMENDED
PREMIUM + ALL REPORTS BUNDLE
$599
Everything in Premium, plus every analysis unlocked.
Everything in Premium
All analyses unlocked
Continuous new analyses as they become available
PREMIUM + ALL REPORTS + 3 YEAR UPDATES
$849
Everything in Bundle, plus automatic updates for 3 years.
Everything in Bundle
Automatic 3-year report updates
1 in 5 people receive a new clinically significant finding within 3 years
CLINICAL STANDARDS
The standard your doctor's lab is required to meet. Ours too.
CLIA Certified
Our laboratory meets Clinical Laboratory Improvement Amendments standards required for all US clinical testing facilities.
ISO 15189 Medical Laboratory
The international standard for medical laboratories, specifying requirements for quality and competence in clinical testing.
30X Clinical Coverage, 99.98% Accuracy
Every base in your genome is read an average of 30 times. The same depth used in diagnostic clinical genomics.
ACMG-Classified Variants
Variants are classified following the American College of Medical Genetics guidelines, the global standard for clinical variant interpretation.
"They never added the numbers up until now when they saw the Dante Labs report."
Thomas spent years with symptoms no specialist could connect. His Dante Labs Whole Genome report identified Noonan Syndrome and a rare leukemia-associated genetic variant that had gone undetected, changing his medical care entirely.
Thomas, Scotland
Queen Elizabeth University Hospital Glasgow, NHS
"The pharmacogenomics report showed my body couldn't process the medication they prescribed after surgery."
Jennifer was diagnosed with breast cancer and underwent treatment. Her Dante Labs pharmacogenomics report revealed she was a poor metabolizer of her prescribed medication, allowing her oncologist to switch to a therapy her body could actually use.
Jennifer, United States
Pharmacogenomics: Breast Cancer Treatment
WHAT YOU RECEIVE
Everything included in your genome test.
Your entire genome, not a slice
We sequence 100% of your DNA at 30X clinical depth. Not a panel. Not an array. Not 0.1% of your genome dressed up as a "DNA test." Every gene, every region between genes.
Reports your doctor can use tomorrow
200+ clinical reports, ACMG-classified, organized by condition category. Designed to be read by physicians, shared with specialists, and acted upon in a clinical setting.
Genome Manager for life
Your secure portal to access, explore, and share your genome data and reports. Available permanently. No expiration, no recurring fee for access.
Re-analysis as science advances
Your DNA does not change, but genomic science is accelerating. As new variant-disease associations are validated, your reports update. Your test becomes more valuable over time.
Your raw data, entirely yours
Download your full genome data (BAM/VCF files) at any time. Your DNA belongs to you. We do not sell, share, or monetize your genetic information.
European data protection
Your data is stored in GDPR-compliant European infrastructure. Fully encrypted at rest and in transit. HIPAA compliant for US customers.
THE PROCESS
From order to answers in four steps.
Order your kit
Choose your plan and we ship your collection kit within 48 hours. Delivered to your home.
Collect your sample
Simple saliva collection at home. No needles, no clinic visit, no appointment needed.
Send it back
Prepaid return shipping included. Your sample is processed in our CLIA-certified, CAP-accredited lab.
Access your results
200+ physician-ready reports delivered to your secure Genome Manager in 6 to 8 weeks.
One test. For life.
Sequenced once at clinical depth. Reports that update as science advances. Choose your plan and get started today.
PREMIUM
$449
ALL REPORTS BUNDLE
$599
3 YEAR UPDATES
$849