Every patient deserves the best answers science can give
Emedgene powers your genomic analysis with machine learning, enabling high throughput analysis and closing the gap between scientific discovery and patient care. Working for you, working for your patients.
Get a Demo
Trusted by the world’s leading genomics institutions
Every patient deserves the best answers science can give
Emedgene powers your genomic analysis with machine learning, enabling high throughput analysis and closing the gap between scientific discovery and patient care. Working for you, working for your patients.
Get a Demo
Trusted by the world’s leading genomics institutions
High throughput genomic interpretation
Automate
A composite of machine learning technologies that automate the variant interpretation workflow, leaving you more time to focus on the insights.
Analyze
This isn’t a self-driving algorithm. Evaluate and control every hypothesis the AI suggests with a full-featured workbench. Implement advanced customization for your lab’s SOP.
Operate
Integrate smoothly and securely with lab operations, existing software and bioinformatics pipelines. Manage team collaboration effectively from sample to report.
It takes diligence to identify a single causative variant among hundreds.
it takes Emedgene to do it 50 times a day.
It takes diligence to identify a single causative variant among hundreds.
it takes Emedgene to do it 50 times a day.
Re-Emedgening genomic interpretation
Pinpoints causative variants
Provides a shortlist of causative variants likely to solve the case, along with supporting evidence from the literature and databases
96%
Recall
Builds Knowledge
An AI knowledge graph codifies the complex and continuously updated web of variants, genes, mechanisms and phenotypes that lie at the heart of the interpretation process.
425K
Entities
Curates Literature
Reads unstructured and structured data from the literature. Data is normalized and made available for analysis in our knowledge graph, following a layer of scientific review.
30%
Unique gene-disease connections
Extracts Phenotypes
Identifies HPO terms in any kind of clinical note, handwritten or typed. Achieves high true positive rate, while maintaining low false positives.
98%
Precision
Re-Emedgening genomic interpretation
Pinpoints causative variants
Provides a shortlist of up to 10 causative variants likely to solve the case, along with supporting evidence from the literature and databases
96%
Recall
New & News
Event
ACMG 2020
ACMG 2020
San Antonio, Texas
March 17-21
Booth 513

Exhibition Theater:
The Utility of Machine Learning for Genomic Analysis and Reanalysis in Clinical Genetics LabsSpeakers:

  • Dr. Linyan Meng, Division Director Clinical Interpretation, Baylor Genetics
  • Dr. Shay Tzur, Chief Science Officer, Emedgene

Thursday, March 19; 12:15 pm – 12:45 pm
Theater #2

Schedule a Meeting
Webinar
ACMG 2020
Breaking the Interpretation Bottleneck
Examining the utility of an automated genomic interpretation algorithm in a clinical genetic lab
Blog
ACMG 2020
Breaking Genes
February 13th, 2020
Yield from CNVs, cross-species approach to rare disease discovery & pan-genomics
Event
ACMG 2020
ESHG 2020
Berlin, Germany
June 6-9, Booth #566
News
ACMG 2020
February 20th, 2020
Inspiring and touching story of one persistent mother and her journey to a rare disease diagnosis at Greenwood Genetic Center with Emedgene AI
New & News
Event
ACMG 2020
ACMG 2020
San Antonio, Texas
March 17-21
Booth 513

Exhibition Theater:
The Utility of Machine Learning for Genomic Analysis and Reanalysis in Clinical Genetics LabsSpeakers:

  • Dr. Linyan Meng, Division Director Clinical Interpretation, Baylor Genetics
  • Dr. Shay Tzur, Chief Science Officer, Emedgene

Thursday, March 19; 12:15 pm – 12:45 pm
Theater #2

Webinar
ACMG 2020
Breaking the Interpretation Bottleneck
Examining the utility of an automated genomic interpretation algorithm in a clinical genetic lab
Blog
ACMG 2020
Breaking Genes
February 13th, 2020
Yield from CNVs, cross-species approach to rare disease discovery & pan-genomics
Event
ACMG 2020
ESHG 2020
Berlin, Germany
June 6-9, Booth #566
News
ACMG 2020
February 20th, 2020
Inspiring and touching story of one persistent mother and her journey to a rare disease diagnosis at Greenwood Genetic Center with Emedgene AI
Used in clinical, translational and research labs
Clinical
Power high throughput genomic analysis and interpretation with the only AI solution tightly integrated into a full-featured clinical workbench.
Research
Accelerate your rate of discovery using a powerful knowledge graph and machine learning driven interpretation
Powered by AI, grounded in science
Breaking the Interpretation Bottleneck
The utilization of WES and WGS in clinical practice has become widespread in recent years. However…
Read abstract
Abstract, October 2019
The use of AI technologies in genomic interpretation
Due to the rapid growth in the use of genome sequencing in medicine, the interpretation workload for gen…
Read abstract
Abstract, October 2018
Powered by AI, grounded in science
Breaking the Interpretation Bottleneck
The utilization of WES and WGS in clinical practice has become widespread in recent years. However…
Read abstract
The use of AI technologies in genomic interpretation
Due to the rapid growth in the use of genome sequencing in medicine, the interpretation workload for gen…
Read abstract
Analysis and reanalysis anywhere, anyone
Schedule a Demo
Analysis and reanalysis anywhere, anyone
Schedule a Demo