Syntes AI unifies clinical records, omics data, lab systems, trial platforms, and regulatory workflows so teams and agents can reason and act with full scientific context.
Cross-Domain Scientific Reasoning
Unify clinical phenotypes, genomic variants, lab results, and trial data into one contextual graph for advanced AI analysis.
Faster Hypothesis Validation
Agents traverse molecular, patient, and historical trial relationships to identify patterns and surface statistically relevant connections.
Reproducible, Traceable AI Decisions
Every insight ties back to source datasets, pipeline versions, documents, and relationships, supporting publication and regulatory review.
Real-Time Trial and Research Monitoring
Connect enrollment, safety signals, site data, protocol deviations, and lab results into a unified operational state.
Governed AI for Regulated Research
Agents simulate impact and enforce policy before modifying data, triggering workflows, or generating regulatory artifacts.
Structured, semi-structured, and unstructured research data coexist in a unified knowledge and context graph.
Agents reason over real relationships—gene ↔ pathway ↔ phenotype ↔ compound ↔ outcome—not isolated records.
Full lineage, version history, and traceable reasoning support FDA submissions and audit processes.
Two-way connectors augment existing data lakes, warehouses, and bioinformatics pipelines without disruption.
