[fusion_fusionslider name=”remarketing-landing-page” hide_on_mobile=”small-visibility,medium-visibility,large-visibility” class=”” id=”” /]

Emedgene’s AI genomic interpretation platform can

dna

Pinpoint Pathogenic Variants

Machine learning algorithms identify pathogenic variants for known and unknown genes

Utilize information from current literature

Natural Language Processing extracts data from scientific publications for use by interpretation algorithms

Improve Novel Gene Discovery

Regularly generate new discoveries by unifying hundreds of data sources in a single AI knowledge graph

Results

160%

Increased yield

through automatic identification of mutations

80%

Time saved

on interpretation & reporting

2X

Novel gene

discovery rate

28M+

Publications

automatically added to the
AI knowledge graph

NEVER A BLACK BOX

The geneticist on the case always knows exactly why a variant is selected by the AI and has direct access to supporting information and literature collected in the knowledge graph.

NEVER A BLACK BOX

The geneticist on the case always knows exactly why a variant is selected by the AI and has direct access to supporting information and literature collected in the knowledge graph.

Re-Emedgene Genetic Interpretation

Re-Emedgene Genetic Interpretation

AI-Based Article Search

Get answers, not data. Clusters results, so you can understand what the literature says on gene, variant, phenotype or disease combinations at a glance. Dig into one Knowledge Collection at a time, or browse through them all.

Reanalysis

Emedgene continues working on unsolved cases automatically or whenever you want. We re-analyze your samples when relevant new scientific findings enter the knowledge graph.

API Integration

Use our AI with your own pipeline, or ours, and hook in to an EMR, LIMS or any other system you have in place.

Free 3 case evaluation for qualifying labs