1x WGS
Low-pass whole genome sequencing for large-scale population studies and screening programs.
- Cost-effective at scale
- Imputation-ready output
- Ideal for biobanks & cohort studies
Business & Enterprise
Enterprise genomic sequencing, built for scale
Trusted by leading research institutions, pharma, and biotech companies for whole genome sequencing services.
Get in touch99%+
of DNA sequenced
600+
peer-reviewed publications
100K+
genomes processed
CLIA
certified U.S. laboratory
Sequencing services
From low-pass screening to ultra-deep oncology sequencing, Nebula Genomics offers flexible whole genome sequencing tiers to match your research goals and budget. All processing takes place in our U.S.-based, CLIA-certified laboratory.
30x WGS
Clinical-grade whole genome sequencing — the gold standard for research and diagnostic applications.
- High-confidence variant calling
- SNVs, indels, and structural variants
- CRAM + VCF deliverables
100x WGS
Ultra-deep sequencing for somatic mutation detection, oncology research, and rare variant discovery.
- 3× deeper than industry standard
- Low-frequency variant detection
- Oncology & rare disease ready
How it works
From initial consultation to secure data delivery, our streamlined process is designed for enterprise reliability and scientific rigor.
01
Consultation
Speak with our sequencing experts to define your project scope, sample requirements, and deliverables.
02
Sample Collection
We provide collection kits and logistics support. Saliva or blood samples — we handle the chain of custody.
03
Sequencing & QC
Samples are processed in our U.S.-based laboratory with rigorous quality control at every stage.
04
Data Delivery
Receive CRAM, VCF, and FASTQ files via secure transfer. Optional bioinformatics analysis and reporting.
Built for your industry
Whether you're running clinical trials, powering academic research, or deploying population-scale screening, our platform adapts to your workflow.
Pharma & Biotech
Accelerate drug discovery and clinical trials with genomic data from sponsored sequencing programs. Participants receive their data at no cost while sponsors gain research-grade insights.
Academic Research
Power observational studies, longitudinal cohorts, and multi-omics research with whole genome data from our U.S.-based CLIA-certified laboratory.
Clinical Diagnostics
Integrate whole genome sequencing into clinical workflows for rare disease diagnosis, pharmacogenomics, and hereditary cancer screening.
Population Health
Deploy large-scale genomic screening programs for health systems, governments, and public health initiatives with cost-effective low-pass sequencing.
Sponsored Sequencing
A new model for genomic research
With Nebula's sponsored sequencing program, research sponsors fund whole genome sequencing for study participants. Participants receive their complete genomic data and personalized reports at no cost, while sponsors gain access to de-identified, research-grade data — creating a win-win for science and individuals.
For Sponsors
Access large-scale, high-quality genomic datasets for drug discovery, biomarker identification, and population studies.
For Participants
Receive free whole genome sequencing, personalized health reports, and full ownership of your genomic data.
For Science
Accelerate research timelines, increase participant engagement, and build diverse genomic cohorts at scale.
Get started
Ready to scale your genomics program?
Our sequencing experts offer free consultations to help you define project scope, sample logistics, and data deliverables. Reach out and let's build something together.
Contact usOr email us directly at business@nebula.org
Our Flagship Test
Unlock your complete genome.
Shop DNA CompleteUnlike traditional DNA tests that analyze only a small portion of your genome, DNA Complete sequences 100% of your DNA, revealing deeper insights into health, traits, ancestry, and new genetic discoveries.
Whole genome sequencing
Continuous report updates
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