MedGenome US is now rebranded as Signios Bio – same team, renewed identity. Click Here

MedGenome US has rebranded to Signios Bio

Integrated multiomics. Driving breakthroughs

Signios Bio, the US arm of MedGenome—a global leader in genetic testing and genomics research—is a multiomics and bioinformatics company dedicated to decoding complex disease biology. We integrate data across genomics, transcriptomics, proteomics, epigenomics, metabolomics, and microbiomics to generate comprehensive insights. Our AI-powered bioinformatics platform uncovers hidden patterns in biological data, accelerating the development of new therapies and diagnostics.

Integrated multiomics. Driving breakthroughs.

Comprehensive, tailored multiomics solutions for research, diagnostics, and beyond

End-to-end multiomics informatics solutions

Signios Bioinformatics: custom analytics, publishable results, and end-to-end research collaboration

  • Data-driven insights: We don’t just provide data; we deliver insights.
    Our customized analysis and visualizations make it easier for you to extract meaningful conclusions and advance your research.
  • Publication-ready results: All our deliverables are designed to be ready for publication, saving you time and ensuring you have high-quality figures and tables to support your research story.
  • Comprehensive support: From experimental design to data interpretation,
    we provide end-to-end support tailored to your specific research needs.

Signios Bioinformatics

Advancing science in critical therapeutic areas

Oncology

Oncology

Sequencing capabilities allow for in-depth investigation into tumor genomics, tumor microenvironments, and molecular pathways driving cancer progression

Immunology

Immunology

Immune profiling of single cells assist in studying immune system dynamics, immune responses, and the mechanisms of immune evasion in cancer

Rare diseases

Rare diseases

Whole genome and exome sequencing to enable discovery of novel genetic mutations and understanding the genetic basis of rare disorders

Neurology disorders

Neurology disorders

Sequencing capabilities allow for in-depth investigation into tumor genomics, tumor microenvironments, and molecular pathways driving cancer progression

Population health & epidemiology

Population health & epidemiology

RWE supports epidemiological studies, population health research, and the development of inclusive therapies that address global health disparities

Pharmagenomics & precision medicine

Pharmagenomics & precision medicine

Multiomics aids in identifying biomarkers for drug efficacy, safety, and dosage optimization, advancing personalized treatment strategies in various therapeutic areas

A snapshot of our impact

10M+

Single-cells sequenced

17M+

Unique variants identified

250,000+

Transcriptomes sequenced

200+

Peer-reviewed publications

1,000+

Citations of our work

500,000+

DNA sequencing assays run

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