sc-batch-integration

Official

Unify 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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