Nebula Explore

The Nebula Explore subscription enables you to get the most out of 30x Whole-Genome Sequencing.
Privacy First. Begin your journey of discovery without risking the privacy of your most personal information.
Nebula Library. Receive weekly updated reports based on the latest scientific discoveries.
Exploration Tools. Use powerful, browser-based genome exploration tools to answer any questions about your DNA.
Deep Ancestry. Discover more about your ancestry with full Y chromosome and mitochondrial DNA sequencing and analysis.
Data Access. Download your FASTQ, BAM, and VCF files and dive deeper into your genomic data.
Already have genomic data? Upload it and get access to the Nebula Library here for free!
Note: All other reporting features are not available for uploaded genomic data.
Nebula Explore
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30x Whole-Genome Sequencing
$299
Pick your Nebula Explore plan:
Get Sequenced
Learn more about Nebula Explore Subscription
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Why 30x Whole-Genome Sequencing?
Nebula Genomics uses next-generation DNA sequencing that determines almost 100% of your DNA. It produces 10,000 times more data than genetic tests based on outdated genotyping technology, and enables the most comprehensive and accurate reporting.
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Privacy First

Nebula Genomics is the leading privacy-focused personal genomics service.

ownership
Take irrevocable ownership of your personal genomic data.
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Control who can access your data and for what purpose it is used.
security
Keep your genomic data protected in a secure computing environment.
Learn about the technology we’re building to protect your DNA
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Nebula Research Library

With the Nebula Explore subscription, you can stay up to date with the most cutting-edge research.

Our team curates the latest scientific discoveries to create your personalized reports. New reports are added every week as scientists publish new research results! The Nebula Research Library already contains over 150 research-based reports.
Explore the Nebula Research Library
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Exploration Tools

Nebula Explore gives you access to powerful tools to explore your DNA and learn at your own pace.

You can use our gene analysis tool to examine any gene of interest, our variant search tool to search your genome for specific genetic variants, and our genome browser to take a direct look at your sequencing data.
Learn more about our exploration tools
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Deep Ancestry

We sequence your entire Y chromosome (Y-DNA) and your mitochondrial DNA (mtDNA).

In partnership with FamilyTreeDNA, we give you access to the world’s largest Y-DNA and mtDNA databases, enable you to trace your paternal and maternal ancestry and connect with your relatives.
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Data Access

30x Whole-Genome Sequencing produces over 100 gigabytes of data. We give you access to all of it so that you can explore it on your own.
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FASTQ File
Your raw sequencing data, generated in our labs.
bam-file
BAM File
Your genome, reconstructed from your sequencing data.
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VCF File
A list of all genetic variants found in your genome.

Nebula Explore

The Nebula Explore subscription enables you to get the most out of 30x Whole-Genome Sequencing.
Privacy First. Begin your journey of discovery without risking the privacy of your most personal information.
Nebula Library. Receive weekly updated reports based on the latest scientific discoveries.
Exploration Tools. Use powerful, browser-based genome exploration tools to answer any questions about your DNA.
Deep Ancestry. Discover more about your ancestry with full Y chromosome and mitochondrial DNA sequencing and analysis.
Data Access. Download your FASTQ, BAM, and VCF files and dive deeper into your genomic data.
Already have genomic data? Upload it and get access to the Nebula Library here for free!
Note: All other reporting features are not available for uploaded genomic data.
Nebula Explore
circle square
product-kit-image
30x Whole-Genome Sequencing
$299
Pick your Nebula Explore plan:
Get Sequenced
Learn more about Nebula Explore Subscription
square

Want to stay updated?

Receive updates about latest additions to the Nebula Library, our work on genomic data privacy, and new reporting features.
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