Patients First & Last

We keep working until the case is resolved

Set a Demo

Patients First & Last

We keep working until the case is resolved

Set a Demo

Patients First & Last

We keep working until the case is resolved

Set a Demo

We deal with the technicalities

So you can focus on the insights

The complexity of analyzing genetic cases today has become unsustainable, as it involves assessing hundreds of facts for each case, and requires deep expertise in different domains. Emedgene workbench was built to remove the inefficiencies and technicalities out of the process, so you can focus on the meaningful data. The Genomic AI assistant pinpoints the few potentially causative mutations, while detailing the underlying logic and supporting evidence as was automatically processed from hundreds of relevant facts.

Unified ontology – no data will pass you by

The emedgene workbench automatically crawls hundreds of resources, including public databases and the written literature, performs automatic conflict resolution and keeps the data in one unified ontology which has all available information required to solve your case.

Unified ontology

Higher case resolution through network sharing and continuous reanalysis of past cases

The emedgene workbench is designed for sharing case data within the emedgene network or publicly. The logic used in solving cases is incorporated into the emedgene Genomics AI, and the knowledge gained is used automatically in similar cases in the future. The emedgene workbench continuously monitors past cases, and as new data is feeded into the ontology, it alerts when new relevant information becomes available.

​Bringing the clinical workflow online

​The emedgene workbench is designed to facilitate communications between various stakeholders working on the same case. The genetic interpreter and patient-facing clinician can communicate directly and in some cases uncover missing clinical information necessary to solve the case.

​Improving productivity via management dashboard

Oversee your organization’s results easily through a dynamic, constantly updated dashboard. The dashboard presents productivity metrics, including: turn around time, team collaboration and diagnostic yield for the various medical conditions.

Our Customers Say

Emedgene is introducing novel applications with the potential to allow clinicians and geneticists perform high-quality analysis of ‘next gen’ data quickly. They are unique in their attempt to implement techniques used in research-based exome analysis in an automated and user-friendly way.  Their most Interesting features are automated reanalysis, prioritization based on both the phenotype and the variant characteristics, and an interactive workflow that can enable a higher diagnosis rate based on additional clinical data.

Karin Weiss MD - Pediatrician and Medical Geneticist, Diplomat of the American Board of Medical Genetics

Emedgene helped our clinical genetic Institute to improve our advanced genetic medicine offering. With emedgene our small team was able to more quickly identify causative mutations, provide clinical interpretation in less time and help more patients. The system is very easy to use, and it helped us improve team communication around patient cases, and was useful for better phenotyping patients. Bottom line – our diagnostic yield is much higher.

Dr. Adel Shalata Pediatrician and Medical Geneticist, Head of The Genetic InstituteBnai Zion Medical Center

I have known emedgene for several years, and I’m pleased to declare that with the help of their excellent platform, I was able to help patients and their families to identify some unique causative variants in unknown genes and to diagnose these patients who went for years undiagnosed. Emedgene is known to me for their commitment and state-of-the-art technology which make emedgene to be in the forefront of science and bring research methodologies to practical use.

Professor Zvi U. Borochowitz, MD, Professor of Pediatrics and Medical GeneticsMedical Genetics Clinic Assuta Medical Center