scanpy

Automates single-cell RNA-seq workflows including QC, normalization, clustering, and annotation using scanpy Python package.

1|Updated Mar 12, 2026
One-click install
npx skills add https://github.com/yf8578/clawomics --skill scanpy-yf8578
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: scanpy
Source: https://github.com/yf8578/clawomics/tree/main/skills/scanpy
Command: npx skills add https://github.com/yf8578/clawomics --skill scanpy-yf8578

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes scripts (resource) and references (resource) and assets (resource) components.

What problem does it solve?

This Skill streamlines the complex process of analyzing single-cell RNA-seq data, enabling researchers to derive meaningful biological insights from high-dimensional datasets.

Core Features & Use Cases

  • End-to-End Analysis: Guides users through the entire scRNA-seq workflow, from QC and normalization to clustering and cell type annotation.
  • Standardized Workflows: Provides pre-built scripts and templates for reproducible analysis.
  • Visualization: Generates publication-quality plots for QC, dimensionality reduction, and marker gene expression.
  • Use Case: A biologist has a new scRNA-seq dataset and needs to identify cell populations, find marker genes for each population, and visualize the results. This Skill can perform all these steps automatically.

Quick Start

Run the standard analysis workflow on your h5ad file.

Frequently Asked Questions about scanpy

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I analyze single-cell RNA-seq data from start to finish?

Single-cell RNA-seq data analysis can be performed end-to-end by running quality control, normalization, dimensionality reduction, clustering, and cell type annotation to derive biological insights from high-dimensional datasets.

What is the best way to identify cell populations and marker genes in scRNA-seq data?

Identifying cell populations and marker genes in scRNA-seq data involves using standardized workflows for clustering and marker gene identification, automatically generating publication-quality visualizations of gene expression.

Can I use scanpy for quality control and normalization of single-cell genomics data?

Scanpy can be used for quality control and normalization of single-cell genomics data, providing pre-built scripts and templates that guide researchers through these essential preprocessing steps reproducibly.

What input formats are supported for single-cell RNA-seq analysis workflows?

Single-cell RNA-seq analysis workflows support various input formats, including h5ad files, allowing researchers to run standard analysis pipelines on high-dimensional datasets to identify distinct cell types.

Does this single-cell analysis pipeline generate publication-quality visualizations?

This single-cell analysis pipeline generates publication-quality visualizations for quality control, dimensionality reduction, and marker gene expression, streamlining the process of deriving biological insights from complex datasets.