NEWThe Complete Baseline

Everyone else sells a snapshot. We build you a baseline.

Forever Labs will map your entire genome and methylation markers today, using your stored biological sample in our lab, and then run future tests to show you how your body is changing.

The Complete Baseline ($2,495 value) is included in every Forever Labs Lifetime Storage Plan.

REPEATATCGGACGTTCG

Methylation, same run

Epigenetic marks read from the same DNA

Base by base

Methyl tags read at each CpG

Long reads, in-house

Span regions short reads miss

30× depth

Every base read about 30 times

30×
every part of your genome, read 30 times over
Long-read
the most powerful sequencing method available
1 sample
your DNA and aging markers, read together
In-house
tested in our own lab, never sent out

The paired sample

Learn how your body is aging, now and in the future.

What other companies do

Testing companies can only measure you as you are on the day they receive your sample.

What Forever Labs does

We keep your original sample. Years from now, as aging clocks and other tests become more powerful, we can run two tests: one on your “future self,” and another on the cells you stored today with Forever Labs.

Your stored sampleEach new sampleYear 3 · Year 6SAME RUNOriginalreferenceYear 32 changedYear 66 changedKey markerChanged from originalNew since last
  1. 1Same tissueAging markers look different in blood than in skin or stem cells, even in the same person. So we compare blood with blood, and cells with cells.
  2. 2Same runWe test your stored sample again alongside the new one, so differences in equipment and chemistry over the years cancel out.
  3. 3Same methodWhen better ways to measure aging arrive, both samples are tested the new way, so your comparison keeps improving.
  1. 1 · Today

    Store and read

    Your sample is stored and your Complete Baseline recorded.

  2. 2 · First follow-up

    Paired run

    A new draw is tested beside a vial of your original.

  3. 3 · Every run after

    Same original

    Each new sample is compared back to the same stored one.

  4. 4 · Over time

    A clearer trend

    Each comparison adds to the record of how your rate of aging is changing.

Stored stem cells with us? We can run the Baseline on your stem cells anytime. If you want to track your aging markers in the future, add a blood or fibroblast baseline now. Every future draw is then compared to its own tissue type.

See your options

What your report shows

Some results you can use now. Others build value over time.

Your genetic results are useful right away. Your aging markers become more useful every time we compare them with a later sample.

Use now

Genome

How you respond to medications

Genes that affect whether a medication works for you and what dose you need.

What you can doShare with your doctor and pharmacist before a new prescription.

Use now

Genome

Genetic findings worth acting on

A physician reviews genes with clear medical guidance, such as inherited cancer risk or high cholesterol.

What you can doIf something is found, confirm it clinically and plan screening.

Use now

Genome

Carrier status

Variants you could pass to a child, even if they never affected you.

What you can doUse it for family planning and share it with relatives.

Genome

What standard DNA tests miss

Large missing or repeated stretches of DNA, plus which parent each change came from.

What you can doStart from a more complete genome, now and for later questions.

Builds over time

Aging markers

Your aging baseline

A record of your aging markers on a set date, read from the same sample as your genome.

What you can doCompare later reads to see how your rate of aging is changing.

Builds over time

Your data

A record that can be read again

We keep your raw data, so better methods can analyze it again without using more of your sample.

What you can doAsk new questions as the science advances.

Beyond your report

Your data can keep answering new questions.

Your report covers what you can act on now. Because we keep your full genome and aging markers on file, we can run more analyses later, with no new sample.

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  1. 1

    Runs on your data

    Genetic risk scores

    How thousands of small genetic differences add up to your risk for conditions like heart disease, type 2 diabetes, and some cancers.

  2. 2

    Runs on your data

    Rare variant search

    A deeper look for rare genetic changes. It can be repeated as medical knowledge grows, or if you or a relative develop an unexplained condition.

  3. 3

    Runs on your data

    Nutrition genetics

    Genes linked to how you process things like caffeine, folate, and lactose. The science is stronger for some than others, and your report says which.

  4. 4

    Runs on your data

    Immune type (HLA)

    The immune genes used to match organ and stem cell donors. They also affect some drug reactions.

  5. 5

    Runs on your data

    Ancestry and lineage

    Your ancestral origins, plus your maternal and paternal lineages, read from your full genome.

  6. 6

    Only with our technology

    Which parent's gene is active

    For some genes, only the copy from your mother or your father is switched on. Because we read your DNA and its markers together, we can see which. Standard tests can't.

  7. 7

    As science advances

    Future aging measures

    New ways to measure biological aging can be applied to your data and your stored sample, so today's baseline works with tomorrow's tools.

  8. How add-ons work

    These analyses aren't part of the standard report. We'll offer them separately as they launch. Any result that could affect your care is reviewed by a physician and confirmed with clinical testing.

From results to action

What happens after your results are ready.

A physician walks you through what your results mean and what to do next.

  1. Step 1

    Your report

    Findings are grouped by what they mean for you, written in plain language, with the technical detail available for your doctor.

    Your completion month

  2. Step 2

    Physician review

    A physician goes through the results with you, explains what matters and what doesn't, and answers your questions.

    After delivery

  3. Step 3

    Your next steps

    Medication notes to share with your doctor and pharmacist, follow-up clinical testing if anything calls for it, and screening or family conversations where relevant.

    With your own doctor

  4. Step 4

    Measure again

    A later sample is tested alongside your stored one, so you can see how you're changing.

    When you choose

Why it's different

Most DNA tests read part of your genome once. We read all of it and keep the record.

One strand, two layers

One long strand of your DNA carries both your genetic code and your aging markers

  • Genetic code
  • Aging markers

Same stretch of DNA, three ways to read it

Only long reads cover a large change from end to end

The same stretch of DNA read three ways. A consumer kit checks a few scattered positions and skips the large change. A standard genome test reads short pieces that break apart at the change. Complete Baseline reads long continuous stretches that span it, with aging markers on the same reads.

How much of your DNA

Consumer DNA kit
A small, preselected set of positions
Standard genome test
Whole genome, in short fragments
Complete Baseline
Whole genome, in long continuous reads

Large DNA changes

Consumer DNA kit
Mostly not detected
Standard genome test
Many missed
Complete Baseline
Found, across long stretches

Aging markers

Consumer DNA kit
Not measured
Standard genome test
Needs a separate test and more sample
Complete Baseline
Read at the same time, from the same DNA

Which parent each gene change came from

Consumer DNA kit
No
Standard genome test
Limited
Complete Baseline
Yes, across long stretches

Raw data kept for future analysis

Consumer DNA kit
No
Standard genome test
Usually just a summary
Complete Baseline
Full raw data saved

Sample kept for future tests

Consumer DNA kit
Discarded
Standard genome test
Discarded
Complete Baseline
Stored in your name

For common risk scores and standard carrier screening, a standard genome test is often enough. Our approach matters most for the large DNA changes other tests miss, for reading your aging markers without a second test, and for keeping a record that can be analyzed again later.

Where your run comes from

From cells already in the vault, or from a simple blood draw.

01

Already a stem cell member

We use the cells you've already stored

We thaw one vial and leave the rest untouched. Your genome reflects the cells as they were on your storage date.

  • No collection, no procedure
  • DNA quality is checked before you're charged the balance
  • Your report notes which sample and tissue was read
02

New to Forever Labs, or adding blood

A 15-minute blood draw

A licensed phlebotomist comes to your home, or you visit a lab near you. We extract DNA from the draw and also store your immune cells and plasma.

  • Included in every Lifetime plan
  • Starts a blood record you can add to with later draws
  • Gives you a blood sample for future aging comparisons

Reserve your run

One instrument, one member at a time.

Each Complete Baseline gets a full run on our sequencer. When you reserve, we schedule your run and confirm the month your report will be ready.

  • Lifetime plans

    The Complete Baseline is included in every new Blood, Fibroblast, and Stem Cell Lifetime plan.

  • Lifetime members

    Refer someone who buys a Lifetime plan by October 15 using your code, and your Complete Baseline is on us.

$2,495

Complete Baseline, as a stand-alone analysis

  • Your entire genome, read 30 times over, plus your aging markers
  • Physician-reviewed report and results session
  • Raw data saved for future analysis
  • For stored samples, we check DNA quality before charging the balance

Pay over time with Klarna or Affirm, subject to approval.

The Complete Baseline ($2,495 value) is included in every Forever Labs Lifetime Storage Plan.

Build your Personal Bio-Vault.

Each collection is stored on its own date. Add another when it makes sense for you.

Before you reserve

No. The Complete Baseline is a member analysis service reviewed by a physician. It isn't a diagnostic test. If your report shows something that could affect your care, your physician can order clinical-grade confirmatory testing before any medical decision is made.

Reserve the run. Keep the younger you on file.

The Complete Baseline is a wellness record reviewed by a board-certified physician partner. It is not a diagnosis.