scientific-single-cell-genomics

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End-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 required

Components

Standard package

💻 Claude Code Installation

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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.
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