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	Sa1216: Development of colorectal cancer and matched healthy organoids from Saudi patients: a case study	Rare disease
	Saudi Summer Internship (SSI)	Opportunities
	Scientific Computing and Machine Learning Research Group	Front Page
	Secure Next Generation Resilient Systems Lab Research Group	Front Page
	Security Research Bearing Experimental Results Research Group	Front Page
	Semantic Disease Gene Embeddings (SmuDGE): phenotype-based disease gene prioritization without phenotypes	Neuro-Symbolic AI, Rare disease
	Semantic integration of physiology phenotypes with an application to the Cellular Phenotype Ontology	Applied Ontology, Ontology engineering
	Semantic prioritization of novel causative genomic variants	Rare disease, Semantic similarity
	Semantic similarity	Semantic similarity
	Semantic similarity and machine learning with ontologies	Applied Ontology, Neuro-Symbolic AI, Semantic similarity
	Semantic Systems Biology: Formal Knowledge Representation in Systems Biology for Model Construction, Retrieval, Validation and Discovery	Applied Ontology, Drug mechanisms
	Semantic units: organizing knowledge graphs into semantically meaningful units of representation	Applied Ontology
	Semi-Supervised Entity Alignment via Knowledge Graph Embedding with Awareness of Degree Difference	Applied Ontology, Neuro-Symbolic AI
	Sensing and Localization	Research
	Sensors Research Group	Front Page
	SIDEKICK: A Semantically Integrated Resource for Drug Effects, Indications, and Contraindications
	Similarity-based search of model organism, disease and drug effect phenotypes	Applied Ontology, Drug mechanisms, Semantic similarity
	Smart Health	Research
	Smart, Advanced Memory devices and Applications lab Research Group	Front Page
	SmuDGE	Biomedical Informatics, Drug mechanisms, Semantic similarity
	Software-Defined Advanced Networked and Distributed Systems Research Group	Front Page
	SPARQL2OWL: Towards Bridging the Semantic Gap Between RDF and OWL	Applied Ontology, Ontology engineering
	Spatio-Temporal Statistics and Data Science Research Group	Info
	Spin-Offs
	Startups
	STARVar	genomics, Phenotype informatics, Rare disease
	Starvar: symptom-based tool for automatic ranking of variants using evidence from literature and genomes	Rare disease
	Statistical Methodology	Research
	Statistics Program	Front Page
	Stochastic Numerics Research Group	Front Page
	Stochastic Processes and Mathematical Statistics	Front Page
	Structural and Functional Bioinformatics Research Group	Front Page
	Student Enrichment and Development	Study
	Su1295: Chemically defined peptide-based matrices enabling the development of colorectal organoid models for therapeutic applications and disease modeling	Drug mechanisms, Rare disease
	Systematic Analysis of Experimental Phenotype Data Reveals Gene Functions