sc-batch-integration
OfficialUnify scRNA-seq datasets
AuthorTianGzlab
Version1.0.0
Installs0
System Documentation
What problem does it solve?
This Skill addresses the challenge of technical variation (batch effects) in single-cell RNA sequencing data, which can obscure true biological differences between samples.
Core Features & Use Cases
- Batch Effect Removal: Integrates multiple scRNA-seq datasets to remove technical variation while preserving biological signals.
- Method Flexibility: Supports various state-of-the-art integration algorithms including Harmony, scVI, Seurat CCA/RPCA, BBKNN, and fastMNN.
- Use Case: Integrate data from experiments run on different days or with different reagent lots to enable a unified downstream analysis, such as identifying cell types or differential gene expression across all conditions.
Quick Start
Run Harmony batch integration on my merged single-cell data.
Dependency Matrix
Required Modules
scanpyanndataharmonypybbknnscanoramascvi-tools
Components
scriptsreferences
💻 Claude Code Installation
Recommended: Let Claude install automatically. Simply copy and paste the text below to Claude Code.
Please help me install this Skill: Name: sc-batch-integration Download link: https://github.com/TianGzlab/OmicsClaw/archive/main.zip#sc-batch-integration Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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