scvi-tools-single-cell

Community

Deep generative models for single-cell omics.

Authorjaechang-hits
Version1.0.0
Installs0

System Documentation

What problem does it solve?

This Skill addresses the complexity of analyzing single-cell omic data by providing advanced probabilistic models for batch correction, cell type annotation, and differential expression analysis, enabling deeper biological insights from noisy, high-dimensional datasets.

Core Features & Use Cases

  • Probabilistic Batch Correction: Integrates multiple scRNA-seq datasets while preserving biological variation (scVI).
  • Semi-Supervised Cell Annotation: Assigns cell types to unlabeled cells using a partially labeled reference (scANVI).
  • Multi-modal Data Integration: Models both RNA and protein expression from CITE-seq data (totalVI).
  • Transfer Learning: Adapts pre-trained models to new datasets efficiently (scARCHES).
  • Differential Expression: Performs statistically grounded DE analysis with uncertainty quantification.
  • Use Case: Integrate 10 different scRNA-seq experiments from varying protocols, identify novel cell subtypes using scANVI, and perform robust differential expression analysis between these subtypes.

Quick Start

Use the scvi-tools-single-cell skill to integrate multiple scRNA-seq batches and visualize the results.

Dependency Matrix

Required Modules

scvi-toolsscanpyanndata

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: scvi-tools-single-cell
Download link: https://github.com/jaechang-hits/SciAgent-Skills/archive/main.zip#scvi-tools-single-cell

Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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