What problem does it solve?
Statistical analyses like differential expression or GWAS produce lists of significant genes and variants, but p-values alone do not explain biological meaning. This Skill bridges that gap by connecting computed results to biological context from ToolUniverse databases, turning raw statistics into mechanistic interpretations.
Core Features & Use Cases
- Multi-Database Evidence Integration: Query UniProt, GO, Reactome, KEGG, ClinVar, OpenTargets, STRING, and PubMed to annotate significant genes, variants, chemicals, and metabolites with function, pathway, and disease context.
- Causal Reasoning Frameworks: Apply DAG construction, triangulation, Mendelian randomization logic, and mediation analysis to move from association toward causal claims.
- Cross-Validation and Graded Reporting: Attempt falsification through replication, genetic support, dose-response, and negative controls, then produce evidence summary tables with strength grades and next-step hypotheses.
- Use Case: After a DESeq2 analysis yields 200 significant genes, use this Skill to annotate them with pathway and disease evidence, check GWAS support, and produce a graded evidence table explaining which findings are mechanistically robust.
Quick Start
Interpret my list of significant genes from this differential expression analysis using ToolUniverse biological databases and produce an evidence-graded report.