Organized Evidence For Medical Genetics
AI collected, curated, and updated evidence to assist medical geneticists, molecular pathologists, genetic counselors, and researchers.
Features
Adenine AI helps experts reach usable genetic and functional evidence with fewer clicks.
Next-generation workflow automation enables daily imports of new evidence.
Documented Web APIs enable integration with any EHR, variant identification, and classification systems.
Find evidence for the difficult-to-assess ACMG codes PP1, PM6, PS2, PS3, PP4, BS3, BS4, and BP3.
How Adenine AI Can Augment Your Variant-Classification SOP?
Experience the power of AI-driven collection and curation of published case-reports, multi-patient studies, and assays. Make informed decision with latest evidence on association of variant and gene with disease. Reach to "relevant" evidence with powerful filters like Patient's age, sex, ethnicity, zygosity, and more.