Genetic variants are small differences in your DNA. Some variants can change how your genes work. This analysis tool uses the AlphaGenome API to find out if a variant affects gene activity or causes disease. It helps scientists and doctors understand the impact of these changes.
The tool checks many types of biological data. It looks at RNA expression, chromatin accessibility, and histone marks. It also studies transcription factors. Researchers can examine non-coding variants that are outside protein-coding regions. These variants are key to understanding many diseases and regulatory functions.
Global
mkdir -p ~/.claude/skills/alphagenome-single-variant-analysisProject
mkdir -p .claude/skills/alphagenome-single-variant-analysisSource Repository
Healthcare Emr Patternsaffaan-m/everything-claude-code
Build safe efficient healthcare EMR systems with proven clinical patterns
Healthcare Cdss Patternsaffaan-m/everything-claude-code
Build patient safety critical CDSS modules with zero tolerance for false negatives
Mfds Food Safetynomadamas/k-skill
Ask about food safety but it interviews you first for symptoms
Mfds Drug Safetynomadamas/k-skill
Check drug safety with official data after a mandatory interview about symptoms
Healthkitdpearson2699/swift-ios-skills
Easily read write and query Apple Health data for health and fitness apps
Sensorkitdpearson2699/swift-ios-skills
Gather sensor data from iOS devices for approved health research studies
Ggetaffaan-m/everything-claude-code
Quick genomic database queries and reproducible bioinformatics lookups with gget
Single Cell Rna Qcanthropics/knowledge-work-plugins
Automatically filter low-quality cells from single-cell RNA-seq data using scverse best practices