multi-omics-integration

Integrate multi-modal omics datasets using MOFA+, DIABLO, and SNF methods.

29|3|Updated Jun 11, 2026
One-click install
npx skills add https://github.com/inflexa-ai/inflexa --skill multi-omics-integration-inflexa-ai
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: multi-omics-integration
Source: https://github.com/inflexa-ai/inflexa/tree/main/skills/multi-omics-integration
Command: npx skills add https://github.com/inflexa-ai/inflexa --skill multi-omics-integration-inflexa-ai

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill requires muon, mofapy2, mixOmics, snfpy, decoupler, networkX, rpy2, and includes references (resource) components.

What problem does it solve?

This skill addresses the complexity of integrating heterogeneous biological data modalities, such as transcriptomics, proteomics, and metabolomics, by providing a structured framework for exploratory, supervised, and network-based analysis.

Core Features & Use Cases

  • Multi-Omics Integration: Supports MOFA+ for unsupervised factor analysis, DIABLO for supervised classification, and SNF for similarity-based patient stratification.
  • Causal Modeling: Provides workflows for inferring signaling topology using CARNIVAL and COSMOS.
  • Use Case: A researcher can use this skill to identify latent factors driving variation across single-cell RNA-seq and ATAC-seq data, or to predict disease outcomes by integrating protein and metabolite abundances.

Quick Start

Use the multi-omics-integration skill to perform MOFA+ factor analysis on the provided MuData object to identify shared latent factors across modalities.

Frequently Asked Questions about multi-omics-integration

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I integrate multi-omics data for cross-modality analysis?

You can integrate multi-omics data using factor analysis, supervised classification, and network fusion methods to explore cross-modality variation and predict biological outcomes from normalized data blocks.

What is the best way to identify latent factors across transcriptomics and proteomics modalities?

Identifying latent factors across modalities is best achieved through unsupervised factor analysis using MOFA+, which finds shared sources of variation driving heterogeneity in multi-modal datasets.

Do I need MuData containers to perform similarity network fusion on multi-omics datasets?

Yes, you need MuData containers to organize pre-normalized data blocks, ensuring consistent cross-modality integration when applying SNF for similarity-based patient stratification.

How does DIABLO supervised classification work for predicting disease outcomes from multi-omics data?

DIABLO performs supervised classification by integrating multiple omics layers to identify correlated multi-omics signatures, enabling predictive modeling of biological outcomes like disease status.

Can I infer signaling topology from multi-omics integration results?

Yes, you can infer signaling topology from integration results using provided causal modeling workflows that calculate signaling networks from multi-omics variation and biological outputs.

What are the limitations of using unsupervised factor analysis for single-cell multi-omics integration?

Unsupervised factor analysis requires pre-normalized data blocks within MuData containers and may not directly predict biological outcomes without subsequent supervised classification or network fusion steps.