Greenomes
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Own your complete DNA record & optimize your health.

Map your entire genome, once from home, to unlock a lifetime of personalized health insights across medicine, nutrition, and performance.

Start My Sequencing View Sample Report

Starting at $166/mo with Affirm

100% Private. Encrypted DNA files, only viewable by you.

CLIA Certified and CAP Accredited Lab

The basics

Your genome, in plain English.

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  1. 01

    What is DNA?

    Your body is built from a genetic code made of four letters: A, T, G, and C. You inherit roughly 3 billion DNA letters from your mother and 3 billion from your father. Together, they are organized into 46 chromosomes and carried in nearly every cell in your body. Those letters form the biological instruction set behind your receptors, enzymes, structural proteins, hormones, and many of the systems that determine how your body functions.

  2. 02

    Genotype vs. phenotype

    You inherit two copies of most genes, one from each parent, called alleles. This exact combination you carry is your genotype. Your phenotype is the measurable part of how that genotype actually surfaces in you. It is why bright light makes some people sneeze or why cilantro tastes like soap to others. Your body carries different combinations of genetic variants. These variants help explain why two people can respond differently to the same medication, food, training, supplements, or sleep.

  3. 03

    How genes build proteins

    Only 1 to 2% of the three billion base pairs codes for proteins. These 20,000 protein-coding genes are the blueprints for every receptor, enzyme, and most hormones in your body. Changes as small as one letter being swapped can change the shape of the protein built or how much is produced. For example, CYP1A2 handles about 95% of caffeine metabolism. One person's allele might crank out plenty of it and coffee barely affects them (a fast metabolizer), while another's makes far less and leaves them wired for hours (a slow one). The same espresso, two completely different experiences.

The effects of your coffee, taste of your cilantro, and timing of your sneeze. All of these are written in letters you have never seen. A complete Greenomes reading shows you exactly which ones you have.

Check Readiness

Why long-read

Long-read sequencing tells your complete story,
unlike other tests

Most tests read a sliver of your DNA in short, broken fragments. Long reads span the whole sequence, so the repeats, structural changes, and look-alike genes that trip up other methods resolve cleanly.

99.95% HiFi base-call accuracy

PacBio HiFi is the new gold standard in genomics: the reach of long reads with the accuracy serious interpretation depends on. It is exactly what Greenomes captures for the file you keep.

Source: PacBio HiFi sequencing.

Short reads leave gaps in coverage, while long HiFi reads span the whole sequence for complete, gap-free coverage. SHORT READS Missing data leaves gaps in coverage Reference genome N N N N N N N N N Sequence gaps remain HIFI READS Long reads span the whole sequence Reference genome Complete coverage, no gaps
Short reads leave gaps. HiFi long reads span the whole sequence, so your genome reconstructs completely.

The dashboard

Insights, not just raw data.

Greenomes reads 100% of your genome with long-read sequencing. A standard at-home DNA kit reads about 0.1%, a thin scan of preselected markers. That is the gap between a curiosity and a clinical-grade record you can actually act on.

  • 100%of your genome sequenced, and every file is yours to keep
  • ~0.1%is all a typical consumer DNA array ever reads
  • 3 lensespharmacogenomics, nutrition, and disease-risk crossover

How it works

From interested to sequenced, in three steps.

Three steps for you, and we handle the rest: at-home sample collection, long-read sequencing through a CLIA-certified lab, and encrypted delivery and storage.

  1. 01

    Readiness

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

  2. 02

    Sample 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. 03

    Delivery

    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.

Your genome, owned for life

Sequence once. Own your DNA record for life.

Create a high-fidelity genome record designed to support more personalized health decisions today, and new insights as medicine, nutrition, and performance science advance.

  • PacBio HiFi long-read sequencing
  • Sequenced in a CLIA-certified laboratory
  • Source files included
  • Private and never sold

Complete Genome Sequencing

20x PacBio HiFi long-read whole-genome sequencing

$1,995

One-time payment. No subscription. Your DNA record and source files are yours for life.

Everything included

  • PacBio HiFi long-read whole-genome sequencing Reads the hard-to-map regions short-read tests leave out.
  • Coordinated at-home blood collection A professional draw arranged at your convenience, no lab trip.
  • FASTQ, BAM, and VCF source files to download and keep The complete, portable record, not just a summary report.
  • Secure digital delivery Encrypted access to your data and results, private to you.
  • Clear, plain-language starting overview What your results mean, written for people, not specialists.
  • Files prepared for future reinterpretation and analysis Structured to be re-read as science and tools improve.
Start Sequencing Not ready to begin? Check your readiness first.

Prefer to pay over time? See if you prequalify with Affirm.

HSA/FSA payment may be available depending on your plan and provider.

One sequencing purchase. A DNA record built to remain useful for years to come.

Estimated turnaround is approximately 12 weeks after sample acceptance. Financing is subject to eligibility and approval. HSA/FSA eligibility depends on the customer's plan and provider.

The best DNA record.

Unlock your full health potential.
Medicine, nutrition, and performance insights designed for you.

Sequence My Genome Readiness Check
PacBio Revio long-read sequencing system