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.

200+

peer-reviewed publications

600,000+

samples sequenced from over 400,000 patients

500,000+

WES, targeted panels & WGS

250,000+

transcriptomes

10M

single-cells sequenced

>10 Petabytes

of genomics data & 10M unique variants identified

1,300+

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

RESEARCH & PHARMA SOLUTIONS

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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PARTNERSHIP

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.

News

Featured articles

Martin Dewhurst MedGenome

NEWS

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

NEWS

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

NEWS

MedGenome to Exhibit Proprietary Sequencing and Informatics Solutions at the AACR 2023
MedGenome Pharma Partneship

NEWS

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

NEWS

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

NEWS

Gallbladder cancer vaccine candidates identified

CONTACT US

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