scientific-single-cell-genomics
CommunityEnd-to-end single-cell RNA-seq analysis workflow.
Authornahisaho
Version1.0.0
Installs0
System Documentation
What problem does it solve?
Provides a standardized, reproducible workflow for scRNA-seq analysis, covering quality control, normalization, dimensionality reduction, clustering, differential expression, and cell-type annotation, all built on the Scanpy/AnnData ecosystem.
Core Features & Use Cases
- QC and preprocessing for scRNA-seq data, ensuring high-quality cells and reliable gene metrics.
- Normalization, highly variable gene selection, PCA/UMAP, and Leiden clustering to reveal cellular heterogeneity.
- Differential expression analysis and cell-type annotation to interpret clusters and cell states.
- RNA velocity integration for lineage trajectory inference and dynamic cellular states.
- Intercellular communication estimation with CellChat/CellPhoneDB to study cellular crosstalk.
- Compatible with Scanpy/AnnData workflows for scalable, reproducible analyses.
Quick Start
Apply the standard scRNA-seq workflow to an AnnData object to generate QC metrics, normalization and HVG selection, PCA/UMAP, Leiden clustering, DEG identification, and cell-type annotation.
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: scientific-single-cell-genomics Download link: https://github.com/nahisaho/satori/archive/main.zip#scientific-single-cell-genomics Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
Agent Skills Search Helper
Install a tiny helper to your Agent, search and equip skill from 471,000+ vetted skills library on demand.