Deep understanding of scientific data, for more clarity
With us, you’re on the right track

Solid clinical decisions require globally connected biomedical knowledge

Biomedical data generated around the world plays a key role in understanding the biology of disease, but its sheer volume and breadth makes connecting relevant knowledge challenging. This is where Molecular Health software applications and services excel. We design and maintain applications for the clinical annotation of genetic variants to support molecular pathologists, oncologists, and other medical professionals in making precision medicine a reality for every patient, and to support human geneticists in identifying cancer predispositions. By mapping the molecular profile of a patient’s tumor or germline to the world’s biomedical knowledge, our applications identify evidence-based and patient-specific treatment options, risk factors, and clinical trial eligibility.

For solid and ​ hematologic cancers​

The comprehensive application for automated interpretation of NGS data from any kind of solid or hematologic cancer
MH Guide quickly and accurately identifies and interprets genetic variants in cancer. The MH Guide report helps treatment providers choose therapy options and clinical trials that match the cancer patient’s molecular profile.
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For hereditary cancers​

Comprehensive applications for automated interpretation of NGS data from hereditary cancers
Our applications support you in identifying clinically-significant germline variants associated with hereditary breast and ovarian cancer syndrome (HBOC), or other hereditary cancers.
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