Disclaimer: For updated information please visit the Nebula Genomics website.
Nebula Genomics provides comprehensive genome sequencing, consistent DNA report updates, and detailed ancestry insights. Their services range from $149 to $999 based on the chosen package.
Established in 2016 by genomics scientist Professor Church, alongside his proteges Kamal Obbad and Dennis Grishin, Nebula Genomics operates out of California. Their mission is to empower individuals to securely share genomic data, thereby amassing extensive datasets crucial for propelling human genetics research forward.
At the heart of Nebula Genomics offerings is an in-depth genome sequencing service, with up to a 100X sequencing depth, ensuring top-notch DNA data precision. Additionally, users can access the Nebula Explore research library, a platform where you can compare your DNA against scientific findings. This can help you derive potential risk evaluations for specific health disorders.
Nebula Explore Research Library: The reports are based on individual research studies. Each report contains information about genes derived from specific study findings.
Update Frequency: New research articles are added to the Nebula library weekly, ensuring that active subscribers always have access to the latest information.
General Overview: Each report begins with a broad overview of the subject and the studies, accompanied by an interesting fact related to the topic. This section also provides your polygenic risk score (percentile) compared to other Nebula Genomics users.
Detailed Analysis: The reports feature tables detailing the genetic findings following the general overview. These tables also indicate your genotype and whether you have an increased or decreased risk for a particular trait.
While the charts provided are informative, the terminology used can be heavily scientific. It may be challenging for users without a background in genetics to understand without a Google search.
Links to Further Information: Each report links to additional resources on the topic, enhancing the depth of information available.
Mini-reports: Apart from the primary reports, Nebula offers mini-reports on various established genetic traits. These mini-reports provide a summary, an associated SNP, and a link to the original study.
Types of Traits Covered: The reports explore various categories, including:
Nebula Genomics has also introduced an ancestry feature. This comprehensive ancestry report draws on Y-chromosome and mitochondrial DNA for its insights. To view your report, go to the ancestry section and choose the ‘My Data’ option. It will show you a detailed breakdown of your ancestry, represented as percentages from various global regions. You can see an illustrative example of the report below:
In addition to analyzing your DNA, Nebula offers insights into the bacteria in your mouth. They utilize the same technology that decodes your DNA to understand the bacterial composition in your saliva sample.
Understanding the oral microbiome is essential. The oral microbiome is associated with conditions such as irritable bowel disease, diabetes, and Alzheimer’s disease.Â
You receive a percentile that compares your oral microbiome with other users. Additionally, the report includes details from selected studies indicating potential links between your oral microbiome and specific health conditions. However, it is essential to remember that this is not intended as a diagnostic tool.
The cost for the DNA test varies depending on sequencing depth:
Outside the USA? Shipping costs are on you. Post-data generation, they provide a 14-day free trial of the reporting service. Post-the-trial subscription fees apply.
All packages come with a Lifetime additional membership fee, which is $200 for the Standard and $275 for the more advanced packages.Â
The standard package does not capture the entirety of your DNA. The distinction between the 30X and 100X packages lies in the confidence level of the data accuracy. Further, if you are outside the USA, Nebula Genomics will not cover your shipping fees.
Upon getting your genetic data, Nebula Genomics offers a 14-day free trial for their reporting service. After this period, the service costs start at $10 monthly, or you can opt for a one-time payment of $200 or $275 for lifetime access.
Should you decide against continuing the membership subscription, you can download and use your data elsewhere. Additionally, Nebula accommodates raw DNA data uploads from different providers.
While whole genome sequencing is pricier than the conventional DNA genotyping methods adopted by companies like 23andMe and LifeDNA, these companies deploy advanced algorithms to produce variations across hundreds of thousands of genetic markers.
The pivotal decision when considering to use Nebula Genomics for a more complete DNA sequencing hinges on the value proposition of whole genome sequencing. It might not be worth it at this time.
Whole genome sequencing has not reached widespread acceptance yet among third parties. So, the downloadable raw data from Nebula may not be compatible with other platforms, as the other popular consumer genetic testing companies prefer data from other types of DNA kits.
The data volume produced by whole genome sequencing is unparalleled. However, the comparative data pool is limited. Additionally, our understanding has not evolved enough to extract insights from vast portions of our DNA. Yet, possessing this data could prove advantageous in future scenarios.
While the WGS data could become more relevant with technology advancements, its cost-effectiveness in 2023 remains debatable.
Nebula Genomics provides an extensive library for customers to compare their genetic data against, helping them discern potential predispositions to specific conditions or traits. It, however, marks the extent of their health insights.
While customers can pinpoint genetic tendencies that may put them at heightened risk for certain health conditions, Nebula falls short in offering additional insights on factors that could amplify or mitigate those risks. The platform does not provide users with tailored advice based on their findings.
This is a significant drawback. Learning that you might be susceptible to specific health challenges without guidance on potential next steps can be confusing and disconcerting.
Leveraging blockchain, Nebula ensures top-tier data security. They promote anonymous genetic sequencing — from payments to browsing. Though they share data with other researchers, user anonymity remains intact.
Are you interested in both on your DNA-based health and ancestry insights? If your focus is more on your personal health aspects, LifeDNA might be a worthy alternative. We provide comprehensive health insights and actionable recommendations, offering a more holistic approach to DNA analysis.
LifeDNA has emerged as a prominent option for analyzing 23andMe raw data, owing to a combination of unique offerings and a commitment to personalized wellness. Here is why many regard LifeDNA as the best option for making the most of your 23andMe raw data:
Further, if you do not have 23andMe raw data, LifeDNA provides that too. Start your personalized wellness journey with LifeDNA’s state-of-the-art DNA kits here.
LifeDNA offers a basic DNA raw data analysis package to kickstart your journey. Users with raw data from 23andMe, AncestryDNA, etc. can access 120+ traits across Nutrition and Allergy, Vitamins & Supplements, Fitness, Sleep, and Skin.
*Understanding your genetics can offer valuable insights into your well-being, but it is not deterministic. Your traits can be influenced by the complex interplay involving nature, lifestyle, family history, and others.
Our reports have not been evaluated by the Food and Drug Administration. The contents on our website and our reports are for informational purposes only, and are not intended to diagnose any medical condition, replace the advice of a healthcare professional, or provide any medical advice, diagnosis, or treatment. Consult with a healthcare professional before making any major lifestyle changes or if you have any other concerns about your results. The testimonials featured may have used more than one LifeDNA or LifeDNA vendors’ product or reports.
