bio-scvi-tools
OfficialDeep generative models for single-cell omics.
Authorbiomaps-infra
Version1.0.0
Installs0
System Documentation
What problem does it solve?
This Skill addresses the complexity of analyzing single-cell omics data by providing advanced probabilistic models for tasks like batch correction, integration, and differential expression analysis.
Core Features & Use Cases
- Probabilistic Modeling: Utilizes deep generative models (VAEs) for robust analysis.
- Data Modalities: Supports RNA-seq, ATAC-seq, CITE-seq, and spatial transcriptomics.
- Use Case: You have multiple batches of single-cell RNA-seq data and need to integrate them, correct for batch effects, and perform differential gene expression analysis between cell types. This Skill provides the tools to achieve this with uncertainty quantification.
Quick Start
Use the bio-scvi-tools skill to analyze single-cell RNA-seq data by setting up AnnData, training an SCVI model, and extracting the latent representation.
Dependency Matrix
Required Modules
None requiredComponents
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: bio-scvi-tools Download link: https://github.com/biomaps-infra/blender-opencode/archive/main.zip#bio-scvi-tools Please download this .zip file, extract it, and install it in the .claude/skills/ directory.
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