Scanpy
Scanpy analyzes single-cell RNA sequencing data to reveal cellular heterogeneity and gene expression patterns, aiding in biological discovery.
Install on your platform
We auto-selected Claude Code based on this skill’s supported platforms.
Run in terminal (recommended)
claude mcp add scanpy npx -- -y @trustedskills/scanpy
Or manually add to ~/.claude/settings.json
{
"mcpServers": {
"scanpy": {
"command": "npx",
"args": [
"-y",
"@trustedskills/scanpy"
]
}
}
}Requires Claude Code (claude CLI). Run claude --version to verify your install.
About This Skill
What it does
This skill provides access to scanpy, a powerful Python library used for analyzing single-cell gene expression data. It enables users to perform tasks such as dimensionality reduction, clustering, and visualization of high-dimensional datasets. The tool facilitates the exploration and understanding of cellular heterogeneity in biological samples.
When to use it
- Analyzing single-cell RNA sequencing (scRNA-seq) data to identify cell types and states.
- Performing quality control and preprocessing steps on scRNA-seq datasets, like filtering cells or genes.
- Creating visualizations such as t-SNE plots or UMAP embeddings to explore cellular relationships.
- Generating reports summarizing the results of single-cell analysis workflows.
Key capabilities
- Data loading and preprocessing for single-cell data.
- Dimensionality reduction techniques (e.g., PCA, t-SNE, UMAP).
- Clustering algorithms to identify cell populations.
- Visualization tools for exploring high-dimensional data.
Example prompts
- "Run scanpy to cluster the provided single-cell RNA sequencing data."
- "Generate a UMAP plot of this scRNA-seq dataset using scanpy."
- "Perform PCA on this AnnData object and visualize the top principal components with scanpy."
Tips & gotchas
- Requires familiarity with Python and basic bioinformatics concepts.
- The skill's effectiveness depends on the quality and preprocessing of the input data.
Tags
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