Target Intelligence Tools
SkillFiles & storageTarget research workflow guide for building compact drug-target dossiers across protein identity, disease evidence, known drugs, interaction partners, pathways, and variant constraint signals. Use when the user asks for a target brief, target validation snapshot, or a one-file summary of what is known about a gene or protein target.
Use Target Intelligence Tools in Claude, ChatGPT or Ahel Desktop
Free. Sign in, add Target Intelligence Tools and connect your AI. About a minute.
Also: Claude Code · Cursor · Codex
Then ask your AI: use the Target Intelligence Tools skill
Details
Instructions available. Your AI can read the instructions. Execution depends on the setup they require.
Account requirements not reviewed. Check the skill instructions before use; Ahel provides instructions and does not run this skill.
No other account needed.
Add Ahel to your AI once: Claude, ChatGPT, Cursor, Claude Code or Codex. Then ask it to use this.
What this skill tells your AI
The instructions your AI receives, as published by drugclaw/drugclaw in skills/research/target-intelligence-tools/SKILL.md and read by Ahel’s review.
Use this skill when the user wants an integrated target brief rather than isolated API hits.
Typical triggers:
- build a quick dossier for a therapeutic target
- summarize what is known about a gene or protein target
- collect disease evidence, known drugs, pathways, and interaction partners in one report
- prepare a target-validation snapshot before docking, screening, or literature deepening
Environment Check
which python3 || true
python3 - <<'PY'
mods = ["requests"]
for name in mods:
try:
__import__(name)
print(f"{name}: ok")
except Exception as exc:
print(f"{name}: missing ({exc})")
PY
If outbound network access is blocked, say so explicitly before claiming the dossier ran.
Bundled Asset
templates/target_dossier.py
Preferred Workflow
- Start from the clearest target identifier available.
- Resolve the target to stable IDs first.
- Pull disease associations, known drugs, pathways, and interaction partners into one markdown dossier.
- Keep the output compact and explicit about missing data.
- Treat the dossier as a research briefing artifact, not a validated decision report.
Quick Start
python3 templates/target_dossier.py \
--query EGFR \
--output targets/egfr_dossier.md \
--summary targets/egfr_dossier.json \
--detail-json targets/egfr_dossier.detail.json
Output Expectations
Good answers should mention:
- the exact identifier or query used
- which stable IDs were resolved
- how many disease, drug, pathway, and interaction rows were found
- whether ClinVar or gnomAD constraint signals were available
- where the markdown dossier and summary JSON were written
Related Skills
For raw UniProt, PDB, ClinVar, gnomAD, Reactome, STRING, or OpenTargets queries, activate bio-db-tools.
For public compound and regulatory APIs such as ChEMBL, BindingDB, openFDA, ClinicalTrials.gov, or OpenAlex, activate pharma-db-tools.
For local variant-callset summarization before target interpretation, activate variant-analysis-tools.
Signals
- GitHub stars
- 125
- Forks
- 9
- Last commit
- Mar 2026
Advanced
- Item type
- skill
- Key
target-intelligence-tools- Source
- github.com/drugclaw/drugclaw
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