Long-read DNA.Longer, healthier life.

The most comprehensive DNA sequencing,revealing health risks before symptoms even appear.

FSA/HSA eligible

100% private, encrypted DNA files

CLIA certified & CAP accredited laboratory

More DNA to learn more about you.

Greenomes uses 20x PacBio Revio™ long-read whole-genome sequencing to provide the most complete DNA record, which you own for life.

1,000xmore DNA sequenced with Greenomescompared to other tests like Ancestry, 23andMe, and others
Greenomes
100% of your DNA
Other tests
Less than 0.1% of your DNA

Our unique long-read sequencing gives complete coverage,
so you don't have any missing gaps.

Short-read DNA sequencing

Missing information
Short-read DNA sequencing leaves three gaps.Ten staggered fragments cover genome coordinates zero to 650 except gaps from 145 to 190, 310 to 355, and 490 to 535. The assembled sequence contains four matching covered segments.Starting genomeGapGapGapAssembled sequence

Long-read DNA sequencing

End-to-End Coverage
Long-read DNA sequencing assembles complete coverage.Three long reads collectively span genome coordinates zero through 650 and assemble into one continuous sequence without gaps.Starting genomeAssembled sequence
99.9%HiFi Read Accuracy

Industry leading,
999 of every 1,000 DNA letters read correctly

PacBio HiFi sequencing is the new gold standard in genomics.
This exceptional accuracy means fewer missed variants, fewer false findings, and the clearest picture of your health.

Source: PacBio HiFi sequencing.

Understand your genome.

Greenomes combines long-read whole-genome sequencing with clear insights across inherited health risk, medication response, nutrition, and performance. You keep the underlying DNA files for future reanalysis.

  • Whole-Genome SequencingA broad view of all your DNA, with no gaps or missing information.
  • Key Health InsightsUnderstand any potential risks now and what to watch over time.
  • Own All Your Data, for Life.You keep your genomic files and revisit them as science advances.
Health overview

Your genetic insights

Illustrative preview
Inherited risk overview2,180 health markers reviewed
Share
6Review
13Typical
7Protective
2,154Low signal

Health library

Search
All 2,180Heart 190Metabolic 57Neurological 942
InsightYour contextSignal
Cardiovascular healthPolygenic context
Within typical rangeTypical
Metabolic healthInherited markers
Worth reviewingReview
Medication responsePharmacogenomics
3 useful findingsReady

What we test.The full picture of your current and future health.

Invest now.Save for you andyour family's future.

Know what to watch for early, while the conversation can still be about prevention rather than treatment.

Three-day hospital stay$30,000

Source: HealthCare.gov, average cost of a three-day hospital stay.

Your complete Greenomes record$2,995

One unexpected hospital stay costs 10x more than your complete DNA record.

From interested to sequenced,in three steps.

  1. 01Readiness

    Start with our 3-minute readiness check so we can best understand your goals, confirm the right workflow, and schedule your sequencing.

  2. 02Sample collection

    We send your at-home collection kit and coordinate delivery to the CLIA-certified lab. You're updated at every step: extraction, sequencing, QC, and review.

  3. 03Delivery

    After sequencing and analysis, your digital record arrives: complete source files, quality metrics, and a plain-English starting report, encrypted, private, and yours to download or access anytime.

The most completeDNA test.

Long-read sequencing to help you live longer and healthier.Own your DNA record without even needing to leave your home. $2,995 total: a $500 deposit today, then $2,495 when laboratory processing begins.

  • HSA/FSA eligible
  • Free shipping
PacBio long-read sequencing systems

Learn you and your family's genetic risks to serious health conditions,
potentially saving you thousands in future medical bills.