Interpret variant pathogenicity from gnomAD CSV exports using ACMG/AMP guidelines, population frequency thresholds, and in silico prediction consensus
Plugin marketplace for the Translational Genomics Group, providing genomics analysis capabilities for Claude Code.
Add the marketplace to Claude Code:
/plugin marketplace add /path/to/tgg-llm-plugins
Or via GitHub (once pushed):
/plugin marketplace add your-org/tgg-llm-plugins
Interpret variant pathogenicity from gnomAD CSV exports using ACMG/AMP guidelines.
Install:
/plugin install variant-interpreter@tgg-plugins
Usage:
/variant-interpret
Then provide the path to your gnomAD CSV file when prompted.
Data Preparation:
Features:
tgg-llm-plugins/
├── .claude-plugin/
│ └── marketplace.json # Marketplace catalog
└── plugins/
└── variant-interpreter/
├── .claude-plugin/
│ └── plugin.json # Plugin manifest
└── skills/
└── variant-interpret/
└── SKILL.md # Skill definition
plugins/.claude-plugin/plugin.json with plugin metadata.claude-plugin/marketplace.jsonInternal use - Translational Genomics Group
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npx claudepluginhub broadinstitute/tgg-llm-plugins --plugin variant-interpretergnomAD MCP server for variant interpretation and population genetics queries
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