DNA Complete (Nebula Genomics) DNA Complete Pro

Whole-genome sequencing and existing-DNA research interpretation.

Visit dnacomplete.com

About DNA Complete (Nebula Genomics)

DNA Complete offers cheek-swab whole-genome sequencing with research reports and exploration tools. Its kit tiers differ in sequencing depth and membership features; DNA Expand instead interprets an existing DNA file without collecting a new sample.

Choose a kit or existing-data uploadSubmit your sample or fileExplore your research reports

Offerings

DNA Complete Pro

$595

initial purchase

Then $195/year

30x average WGS

250+ advertised research reports

At-home 30x average whole-genome sequencing with research reports and required membership.

What’s included in DNA Complete Pro

Included

Cancer Partial

29 reports, including Risk score: Aerodigestive squamous cell cancer; Risk score: Bladder cancer; Risk score: Bone cancer; Risk score: Brain cancer; Risk score: Breast cancer; …

Heart and blood vessels Partial

22 reports, including Risk score: Aortic calcification/atherosclerosis; Risk score: Aortic stenosis; Risk score: Apolipoprotein A-I level; Risk score: Atrial fibrillation; Risk score: Brugada syndrome; …

Brain health Partial

Alzheimer's (APOE) (Risk score: Alzheimer’s disease; Risk score: Resilience to Alzheimer’s disease); Parkinson's disease (Risk score: Parkinson’s disease)

Metabolic health Partial

Celiac disease (Risk score: Celiac disease); Type 2 diabetes (Risk score: Diabetes (Type 2))

Ancestry Included

Regional Ancestry; Ancestry Timeline; Detailed Migration Paths; Famous relatives

Alzheimer's (APOE) Partial

Risk score: Alzheimer’s disease; Risk score: Resilience to Alzheimer’s disease

Not included

Carrier screening
Medication response
Rare-disease screening
Hereditary cancer assay scope
30x-average WGS input, not chip genotyping. No interpreted whole-gene region specification or per-report variant count is published; raw sequence/gene-browser capability does not establish the report.
Inherited heart assay scope
30x-average WGS input, not chip genotyping. No interpreted whole-gene region specification or per-report variant count is published; raw sequence/gene-browser capability does not establish the report.
Carrier screening assay scope
30x-average WGS input, not chip genotyping. No interpreted whole-gene region specification or per-report variant count is published; raw sequence/gene-browser capability does not establish the report.

Before you buy

Before starting
Follow the supplied instructions. The lab must receive the sample within six months of purchase; late samples can void testing/refund eligibility. No fasting or medication change is established here.

Results

Report

Health-report example
Health-report example

An illustrative report connects a genetic finding with the underlying study.

Official examples
Health-report example
Results
Email notification and self-service web reports; optional counselor add-on is separate.
Access
WebEmail
Download
CRAM and VCF advertised; download before membership expires
Timing
No firm current processing interval published

Collection

For a new sequencing purchase, collect cheek swabs at home and return the registered kit. DNA Expand instead uses an existing DNA-file upload.

Reviews

What people complain about

Months without results

Customers repeatedly describe lengthy waits after the laboratory receives their sample, with some still waiting many months later without the results or raw data they expected.

Updates without a clear timeline

Reviewers say support replies can be vague or repetitive, leaving them unsure whether testing is progressing and when they should realistically expect their results.

Refunds can become a dispute

Some customers describe difficulty getting money back after prolonged delays, with accounts of refused refunds or turning to their card provider to resolve the purchase.

Stories

A Nebula Genomics customer

An explanation for recurring muscle symptoms

After studying her Nebula Genomics data, this customer found an RYR1-related explanation for recurring muscle symptoms and had the findings checked by a clinical geneticist. She says it helped her get suitable physical therapy and avoid overtraining weakened muscles.

reddit.com

Laura

Putting genetic risk reports alongside family history

Laura explored Nebula Genomics’ whole-genome reports and found a blood-pressure predisposition that made sense alongside her parents’ health history. The information gave her questions and potential next steps to discuss with her health care providers.

daybydayinourworld.com

Things to know

  • Cancel renewal at least a day in advance.

    Sales are generally final. Download needed files before paid access and storage end.

  • Membership renews until canceled.

    Continuing reports and tools depend on the membership selected.

  • Research and service processing have different rules.

    Identifiable research requires consent; service processing and some de-identified research have separate terms.

  • This purchase provides research interpretation.

    Return the registered person’s sample within six months of purchase.

Alternatives

FAQs

Does this sequence my DNA again?

This kit advertises whole-genome sequencing at 30x average depth. Coverage varies by region/sample; the result is not a clinical diagnosis.

Can I keep access without renewing?

Access continues through your paid term after cancellation. Reports/stored data can be deleted afterward; download needed files before expiry.

Are clinical screening panels included?

These purchases provide research interpretation, disease-risk associations and gene-exploration tools. A clinical carrier or inherited-condition screen is a different service.

Is genetic counseling included?

A separate optional counselor session is advertised; price and duration are unpublished. Elite offers a discount.

What if my sample fails?

The current policy allows discretionary recollection/replacement or other remedies. A free repeat or automatic refund is not guaranteed. The six-month sample receipt deadline applies.