Put Your Nebula Genomics VCF Back to Work
If you exported a single-sample whole-genome VCF from Nebula Genomics, you can upload it directly to Genomisaur. The same VCF works with every Health Report tier and both Family Report tiers, so you do not need a new sequencing kit just to get more reports from data you already own.
At a glance
You still have your Nebula single-sample VCF and want health, trait, or two-parent preconception reports without re-sequencing.
You need a new sequencing run and want the sequencing provider to bundle its own ongoing report platform.
Pricing
Public list prices. Genomisaur Health Reports are $20–$29.99 one-time.
| Option | Price | What it is |
|---|---|---|
| Genomisaur — Full Health Report | $29.99 one-time | 71 PRS + trait predictions from your existing Nebula WGS VCF; +$20 WGS processing |
| Nucleus Genomics (new WGS) | $399 + $39/yr | Fresh WGS + report platform |
| Dante Labs (new WGS) | ~$430 | Clinical 30× WGS + 200+ reports |
| Sequencing.com (VCF upload) | Free upload; apps $5–$99 each | App marketplace with 300+ report apps |
Competitor prices are public list prices from each vendor's site as of 2026 and change often; confirm on the vendor's site before purchasing.
Feature comparison
Side-by-side on the things that actually change what the product does for you.
| Feature | Genomisaur | Nebula Genomics | Edge |
|---|---|---|---|
| Accepts an existing Nebula WGS VCF? | Yes — single-sample .vcf/.vcf.gz | Varies | |
| Report types supported | Every Health and Family report tier | Varies | |
| Need a new DNA sample? | No, if you kept your VCF | Nucleus + Dante: yes | |
| Polygenic risk scores | 71 PRS across 14 categories | Varies | |
| Subscription required | No | Nucleus: $39/yr. Sequencing.com: per-app or subscription. | |
| Turnaround | ~20 min after upload | Weeks (re-sequencing) or variable |
What each one does well
Genomisaur
- Directly accepts a single-sample Nebula WGS VCF or VCF.GZ
- Every individual and family report tier supports WGS
- $29.99 one-time
- No subscription, no ongoing membership
Nebula Genomics
- Nebula Genomics now operates through DNA Complete and offers new WGS kits and its own report library
- Other sequencing and upload platforms may offer broader rare-variant or a-la-carte report catalogs
Frequently asked questions
Is Nebula Genomics still operating?
Yes. Nebula Genomics currently operates with DNA Complete and offers new WGS kits and reports. If you already downloaded a Nebula VCF, it remains portable and can also be analyzed by Genomisaur.
What if I lost my Nebula VCF?
Without a usable VCF, you need to recover the export from your account or obtain a new sequencing run. Genomisaur analyzes existing data; it does not create a VCF from FASTQ, BAM, or CRAM files.
What other Nebula alternatives exist for uploading?
Genomisaur accepts single-sample Nebula VCF/VCF.GZ files for every report type. Sequencing.com also accepts VCFs for its app marketplace. Other services vary, so check their exact file and genome-build requirements.
Can I use my Nebula VCF for a family report?
Yes. Either or both parents can upload a single-sample Nebula WGS VCF. WGS+WGS and mixed WGS+consumer-array couples are supported in both Family Starter and Family Full.
Informational, not diagnostic
Consumer genetic reports — ours, Nebula Genomics's, and others — are informational. Carrier and polygenic risk results should be discussed with a qualified healthcare provider or genetic counselor before making medical or reproductive decisions.