OMIM Explorer ([ Ссылка ]) is an integrative AI recommendation engine webtool for data-driven decisionmaking in clinical diagnostics, variant prioritization, and gene-phenotype association discovery. It was built by Regis A. James ([ Ссылка ]) in the Chad Shaw computational genomics lab at Baylor College of Medicine in Houston, Texas.
Source websites:
• OMIM (the Online Mendelian Inheritance in Man): [ Ссылка ]
• The Human Phenotype Ontology: [ Ссылка ]
• Bio-Lark Concept Recognizer: [ Ссылка ]
OMIM Explorer Overview
Теги
personal genomicsclinical diagnosticsvariant prioritizationhealthcarebiomedical researchexomegenomephenotypegenotypehuman phenotype ontologygenetic variantsOMIM : Online Mendelian Inheritance In Man (Website)Health (Industry)omimHealth Care (Industry)Tutorial (Media Genre)diseaseclinical decision supportprotein-protein interaction