single-cell-multi-omics-analysis-scvi

Community

Probabilistic models for single-cell multi-omics.

AuthorPharMolix
Version1.0.0
Installs0

System Documentation

What problem does it solve?

scvi-tools provides probabilistic models for integrated single-cell multi-omics data, enabling robust joint analysis of RNA, chromatin accessibility, and protein measurements while simplifying batch correction and data integration.

Core Features & Use Cases

  • Supports single-cell RNA-seq, ATAC-seq, and multimodal data (CITE-seq, multi-omics) with unified APIs for setup, training, and extraction.
  • Enables end-to-end workflows for batch correction, data integration across experiments, and cell-type annotation in multi-modal datasets.
  • Supports spatial transcriptomics analysis and specialized modalities via structured model families like scVI, scANVI, totalVI, and MultiVI.

Quick Start

Load your AnnData object with raw counts and follow the standard scvi-tools workflow to obtain a batch-corrected latent representation.

Dependency Matrix

Required Modules

None required

Components

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: single-cell-multi-omics-analysis-scvi
Download link: https://github.com/PharMolix/OpenBioMed/archive/main.zip#single-cell-multi-omics-analysis-scvi

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