Tooluniverse Crispr Screen Analysis
Analyzes CRISPR screen data from ToolUniverse experiments to identify gene essentiality and potential therapeutic targets.
Install on your platform
We auto-selected Claude Code based on this skill’s supported platforms.
Run in terminal (recommended)
claude mcp add tooluniverse-crispr-screen-analysis npx -- -y @trustedskills/tooluniverse-crispr-screen-analysis
Or manually add to ~/.claude/settings.json
{
"mcpServers": {
"tooluniverse-crispr-screen-analysis": {
"command": "npx",
"args": [
"-y",
"@trustedskills/tooluniverse-crispr-screen-analysis"
]
}
}
}Requires Claude Code (claude CLI). Run claude --version to verify your install.
About This Skill
tooluniverse-crispr-screen-analysis
What it does
This skill enables AI agents to analyze CRISPR screen data, helping researchers interpret genetic perturbation results. It processes raw screening outputs to identify significant gene hits and potential biological mechanisms.
When to use it
- Analyzing large-scale CRISPR knockout or activation datasets to find disease-associated genes.
- Identifying candidate therapeutic targets from high-throughput genetic screening results.
- Validating experimental hypotheses by correlating screen hits with known pathway databases.
- Automating the initial interpretation of wet-lab CRISPR experiments before manual review.
Key capabilities
- Processes raw CRISPR screen data formats (e.g., count matrices, enrichment scores).
- Identifies statistically significant gene hits based on user-defined thresholds.
- Integrates with external biological knowledge bases for functional annotation.
- Generates summary reports highlighting top candidates and confidence scores.
Example prompts
- "Analyze this CRISPR screen dataset and list the top 10 most significant gene hits."
- "Interpret these enrichment scores and suggest potential pathways involved in cell survival."
- "Compare the results of two different CRISPR screens to find overlapping gene targets."
Tips & gotchas
Ensure your input data is properly formatted (e.g., tab-separated count matrices) before analysis. This skill works best when combined with domain-specific knowledge to validate biological relevance of identified hits.
Tags
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| Snyk | Pass |
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