Discover How The Latest Genomic Research Can Be Applied To Your Test Results To Get Continuously Increasing Insight Into Your Genetics

The Nebula Library is the only way to stay up-to-date on what the newest research is saying about your DNA. By subscribing, you get personalized, regular updates that keep you on the cutting edge of genomics.
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  • All updates are curated and vetted by our team of scientists.
  • Full access to easy-to-read summaries of new research with a special emphasis on what it means for your results.
  • Unlike other genetic tests, we analyze 100%* of your DNA. That means our reports include 10,000 times more data than 23andMe, AncestryDNA, and others.

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Unlock more from your DNA test with the Nebula Explore™ Reporting Membership.
Get personalized reports based on the latest genomic research to optimize your specific health areas.
Nebula Genomics Exclusive
The most comprehensive DNA tests available that decode 100%* of DNA
Best for
Amount of DNA Decoded
DNA sequencing depth
Ancestry reports
Accuracy of DNA sequencing and reports
Decodes all ~20,000 genes
Identifies common genetic mutations
Identifies rare genetic mutations
Access to genome exploration tools
Ready for diagnostics
New DNA reports are available regularly
Oral microbiome report
Privacy-preserving technologies to protect your genetic information
Nebula Explore™ Reporting Membership
Genome Sequencing Kits

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% off average industry pricing
Whole Genome Sequencing
$249 6371
Plus Nebula Explore™ Membership
  • Deep ancestry report
  • Detects all predispositions
  • Detect rare genetic mutations
  • High accuracy
  • Requires Nebula Membership
Membership: 3 Year+ ($200)
Total: $275
Why is there a membership?
% off average industry pricing
Ultra Deep
Whole Genome Sequencing
$899 21021
Plus Nebula Explore™ Membership
  • Ultra deep ancestry report
  • Detects all predispositions
  • Detect rare genetic mutations
  • Ultra high accuracy
  • Requires Nebula Membership
Membership: 3 Year+ ($200)
Total: $275
Why is there a membership?
Nebula Explore™ Reporting Membership Separate

Membership is required to access your personalized reports and exploration tools that will enable you to examine any of your ~20,000 genes.

Membership begins when sequencing is completed. Сancel auto-renewal anytime.

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Personalized and easy to understand

We curate the latest scientific discoveries to create easy-to-read, personalized reports based on the analysis of your DNA data.

New reports are added regularly as scientists publish new research results and we further interpret your genetic data.

Why Is The Whole Genome Sequencing DNA Test
Superior To Other Tests?

Whole Genome Sequencing decodes all 6.4 billion DNA base pairs in the human genome including the complete set of all 20,000 genes, mitochondrial DNA, and the Y chromosome.

Other consumer genetic testing companies that decode less than 1% of your DNA!

Personal genome sequencing enables the discovery of all genetic variations in every individual gene and produces the most comprehensive and accurate genetic test results.

Preview of the latest discoveries
Lewy body dementia (Chia, 2021) – Is LBD genetic?
Eye color (Simcoe, 2021) – Is eye color genetic?
Type 2 diabetes (Spracklen, 2020) – Is Type 2 Diabetes Genetic?
Type 2 diabetes (Vujikovic, 2020) – Is Diabetes Genetic?
Keratoconus (Hardcastle, 2021) – Is keratoconus genetic?
Addison’s disease (Eriksson, 2021) – Is Addison’s genetic?
What is Genomic Research?

Genomic research is the study of DNA sequences to determine the function of genes. Many genomic research studies focus on identifying specific genes that can predispose an individual to certain diseases. Knowing your risk can help you and your doctor design monitoring, prevention, and treatment plans, especially if you have a history of certain conditions in your family.

The field of genomic research began with the human genome project, the effort to sequence the entire human genome, which was completed in 2003. Advances in genomics research seek to understand the significance of minute differences in the human genome sequence. Most genetic variants are single nucleotide polymorphisms (SNPs), a case in which a single nucleotide in the sequence varies. Even just one difference can influence predisposition to disease or other traits.

Researchers in this field use computers and math techniques called bioinformatics to analyze whole genomes, not just individual SNPs. By analyzing huge amounts of data included in the genome, they can identify more genetic influences on health at a larger scale.

An incredible amount of research on genes and the human genome is being conducted every day. With the sequencing of the human genome, you have access to every genetic variant in your DNA. Using this information, you can compare your results to the latest genomic research to discover more about how your genetic blueprint influences your health.


1) Who is Nebula Genomics?
2) Is your service available in my country?
3) What is Whole Genome Sequencing DNA Testing?
4) How is a Whole Genome Sequencing test done?
5) What can Whole Genome Sequencing DNA Testing reveal about health?
6) What can Whole Genome Sequencing DNA testing reveal about ancestry?
7) I am interested in a specific gene. Can you decode that gene and identify mutations?
8) What is the cost of a Whole Genome Sequencing DNA test?
9) Why is there a subscription? What happens if I cancel my subscription?
10) Does it make sense to purchase Whole Genome Sequencing if I already uploaded my DNA data?
11) What is the difference between 30x and 100x Whole Genome Sequencing?
12) Can I upgrade from 30x to 100x Whole Genome Sequencing?
13) How long does Whole Genome Sequencing take?
14) Does a Whole Genome Sequencing DNA test include mitochondrial DNA?
15) Does health insurance pay for Whole Genome Sequencing?
16) Can I purchase Whole Genome Sequencing as a gift for someone else?
17) Can I partner with you to sequence a large number of samples?
18) I still have not received my package, what do I do?
19) What is your return policy?

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