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Integrate computed statistical results (DEGs, GWAS hits, associations) with biological context from ToolUniverse databases (UniProt, GO, Reactome, ClinVar, OpenTargets).
Passed 3 of 8 test cases with the skill, and 5 of 8 without it.
2 fixed5 passed either way7 still failing8 broke
Tokens, turns and time describe resource use, not a dollar price.
One of 2 test cases the skill fixed. Same model, same prompt, with and without the skill.
I have 3 top GWAS hit variants from our type 2 diabetes study. I need you to outline the structured summary table format required to present these integrated findings clearly to clinical investigators.
| Checked | Without skill | With skill |
|---|---|---|
| The response structures the summary table with columns for statistical evidence, biological mechanism, literature support, genetic support, and evidence grade. | Missed | Passed |
The instructions your model reads when the skill loads.
When analysis requires computation (statistics, data processing, scoring, enrichment), write and run Python code via Bash. Don't describe what you would do -- execute it and report actual results. Use ToolUniverse tools to retrieve data, then Python (pandas, scipy, statsmodels, matplotlib) to analyze it.
Bridge the gap between statistical results and biological understanding. After any computational analysis produces significant findings, this skill teaches how to interpret them using ToolUniverse's biological knowledge tools -- the key advantage over platforms that only do data analysis.
IMPORTANT: Always use English terms in tool calls (gene names, pathway names, organism names), even if the user writes in another language. Respond in the user's language.
Apply when:
NOT for (use other skills instead):
tooluniverse-statistical-modeling or tooluniverse-rnaseq-deseq2tooluniverse-gene-enrichmenttooluniverse-literature-deep-researchtooluniverse-variant-interpretationMap each type of significant finding to the right biological question:
| Finding Type | Biological Question | Tool Discovery Query |
|---|---|---|
| Significant gene list | What pathways are enriched? What functions converge? | find_tools("gene enrichment pathway analysis") |
| Significant variant (rsID) | What is the functional impact? Which gene is affected? | find_tools("variant annotation functional impact") |
| Significant exposure/chemical | What is the biological mechanism? Which pathways? | find_tools("chemical gene pathway toxicology") |
| Significant drug association | What is the molecular target? What is the MOA? | find_tools("drug target mechanism action") |
| Significant metabolite | Which metabolic pathway is perturbed? | find_tools("metabolite pathway identification") |
test cases passed, vs 5 / 8 without
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