Reliable multiomics data at scale

Global genomics solutions provider trusted by leading pharmaceutical and academic researchers

As your research partner, we offer vast experience building prospective disease cohorts for gene discovery programs.


peer-reviewed publications


samples sequenced from over 400,000 patients


WES, targeted panels & WGS




single-cells sequenced

>10 Petabytes

of genomics data & 10M unique variants identified


genetic tests (RUO)

US based

Sequencing lab in California

Our Customers

Enduring partnerships with satisfied customers

A Next Generation Sequencing partner

Your science. Our passion.

Our state-of-the art sequencing facility in California is committed to delivering the highest quality NGS data with industry leading turnaround times by leveraging our optimized workflows and protocols. We offer comprehensive bioinformatics solutions to transform data into insights.

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Transcriptomics services
Transcriptomics services
Spatial transcriptomics services
Spatial transcriptomics services
WGS/WES services
WGS/WES services
Single cell services
Single cell services
Immune profiling services
Immune profiling services
Epigenomics solutions
Epigenomics solutions

Bioinformatics solutions

From data to insights


Multiomic solutions for discovery research

Expert multi-disciplinary team of biologists, geneticists, bioinformaticians, and project managers with a proven track record.

  • Antibody discovery
  • De novo gene assembly and annotation
  • Rare disease research
  • Gene panels
  • Target and biomarker discovery
Genomics Scientist

We support your research accross applications

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Your committed expert partner

We help you accelerate discovery and bring drugs to market faster.

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Unparalleled breadth of expertise & innovation
Unparalleled breadth of expertise & innovation
  • Continuous innovation to optimize the latest genomic assays.
  • Routine & niche high-quality multiomics solutions.
  • Deep bioinformatics: AI/ML-based tools to transform data into insights.
Highly efficient (fast and cost-effective) workflows
Highly efficient (fast and cost-effective) workflows
  • Reliable and fast results.
  • Highly automated and cost-efficient.
  • Streamlined customer engagement through customer portal.
Genomics Partner
The most extensive and diverse genomic dataset
  • 600,000+ sequenced samples from over 400,000 patients.
  • We partner with 500+ hospitals and 5,500+ clinicians worldwide to run thousands of genomic tests per year.
Flexible, consultative customer services
Flexible, consultative customer services
  • PhD level staff scientists for expert consultation.
  • Dedicated Single point of contact with deep technical and scientific expertise.


Featured articles

Grant Winner Dr. Lauren Esposito


MedGenome announces de novo Genome Assembly and Annotation Grant winners for 2024
Foster City Award


MedGenome Inc., honored with the Best of Foster City Award six times in a row
Martin Dewhurst MedGenome


MedGenome appoints Martin Dewhurst as Chairman of Advisory Board
10X Certified MedGenome


MedGenome achieves 10x Genomics Certified Service provider qualification for single cell sequencing
MedGenome Pharma Partneship


MedGenome ties-up with Emmes to bridge gaps in rare diseases
MedGenome Grant


MedGenome, in collaboration with PacBio, announces a de novo genome assembly and annotation grant
Biomarker Discovery Research


Gallbladder cancer vaccine candidates identified


Work with the multiomics specialists

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