bio-workflows-scrnaseq-pipeline
CommunityEnd-to-end scrnaseq workflow to cell types.
Authorya-way
Version1.0.0
Installs0
System Documentation
What problem does it solve?
This workflow processes single-cell RNA-seq data from 10X Cell Ranger outputs to annotated cell types, automating QC, normalization, clustering, marker detection, and annotation to reduce manual effort and improve reproducibility.
Core Features & Use Cases
- End-to-end processing of 10X scRNA-seq data from raw counts to annotated cell types using Seurat (R) or Scanpy (Python).
- Integrated QC, doublet detection, normalization, HVG selection, dimensionality reduction, clustering, and marker-based annotation.
- Real-world use case: a lab processes multiple PBMC samples to identify cell-type composition and novel clusters across conditions.
Quick Start
Run this pipeline on your 10X Cell Ranger output to obtain annotated cell types.
Dependency Matrix
Required Modules
None requiredComponents
Standard package💻 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: bio-workflows-scrnaseq-pipeline Download link: https://github.com/ya-way/cytoclaw-skills/archive/main.zip#bio-workflows-scrnaseq-pipeline Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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