single-cell-multi-omics-analysis-scvi
CommunityProbabilistic models for single-cell multi-omics.
Data & Analytics#single-cell#batch-correction#scvi-tools#multi-omics#probabilistic-modeling#scrna-seq
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 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: 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.
Agent Skills Search Helper
Install a tiny helper to your Agent, search and equip skill from 471,000+ vetted skills library on demand.