1x WGS
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 touch100%
of DNA analyzed
400+
curated reports from peer-reviewed publications
100K+
genomes processed
CLIA
certified U.S. laboratory
Sequencing services
From population screening to ultra-deep whole genome sequencing, Nebula Genomics offers flexible whole genome sequencing tiers to match your research goals and budget. All processing takes place in a 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 and rare variant discovery.
- 3× deeper than industry standard
- Low-frequency variant detection
- Rare disease research 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 samples — we handle the chain of custody.
03
Sequencing & QC
Samples are processed in a 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.
Academic Research
Power observational studies, longitudinal cohorts, and multi-omics research with whole genome data from a U.S.-based CLIA-certified laboratory.
Health & Wellness
Integrate whole genome sequencing into health and wellness programs, from pharmacogenomics and preventive screening to personalized nutrition and lifestyle insights.
Population Health
Deploy large-scale genomic screening programs for health systems, governments, and public health initiatives with cost-effective sequencing.
Full-Service Sequencing
Custom solutions & integrations
As a full-service provider of Whole Genome Sequencing solutions, we offer researchers and businesses unparalleled convenience and added-value services, from at-home sample collection to consumer-friendly reporting and 300+ actionable health reports for every participant.
Sample Collection
At-home saliva kits with full logistics support. No clinic visits required — we handle the chain of custody end to end.
Custom Reports
Build tailored reporting packages for your cohort. Choose from 400+ existing reports or work with our team to develop custom panels specific to your research endpoints.
White-Label & Branding
Fully branded sequencing kits, reports, and participant portals — your logo, your colors, your experience.
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 analyzes 100% of your DNA, revealing deeper insights into health, traits, ancestry, and new genetic discoveries.
Whole genome sequencing
Continuous report updates
Built on Nebula research
Professor George Church, Founder of Nebula Genomics
Image Credit – Christopher Michel