tooluniverse-multi-omics-integration

Integrate transcriptomics, proteomics, methylation, and CNV data for cross-omics correlation and clustering.

1.7k|254|Updated Mar 3, 2025
One-click install
npx skills add https://github.com/mims-harvard/ToolUniverse --skill tooluniverse-multi-omics-integration
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: tooluniverse-multi-omics-integration
Source: https://github.com/mims-harvard/ToolUniverse/tree/main/plugins/tooluniverse/skills/tooluniverse-multi-omics-integration
Command: npx skills add https://github.com/mims-harvard/ToolUniverse --skill tooluniverse-multi-omics-integration

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill requires scipy, numpy, pandas, scikit-learn, and includes references (resource) components.

What problem does it solve?

Analyzing multiple omics datasets in isolation misses cross-layer biological signals like RNA-protein discordance, methylation-driven repression, and CNV dosage effects. This Skill orchestrates per-layer analysis and then performs cross-omics correlation, multi-omics clustering, and pathway-level integration to produce a unified systems-biology interpretation.

Core Features & Use Cases

  • Cross-Omics Correlation: Computes RNA vs protein, methylation vs expression, and CNV vs expression correlations with concordant/discordant gene identification.
  • Multi-Omics Clustering: Applies MOFA+, joint NMF, or SNF for patient subtyping across heterogeneous molecular layers.
  • Pathway & Biomarker Integration: Aggregates multi-omics evidence at the pathway level and selects cross-omics features for classification.
  • Use Case: Integrate TCGA RNA-seq, proteomics, methylation, and CNV data for a cancer cohort to identify patient subtypes, cross-omics driver genes, and multi-omics biomarkers with a structured final report.

Quick Start

Ask the agent to integrate your RNA-seq, proteomics, and methylation datasets, match common samples, run cross-omics correlations and MOFA+ clustering, and generate a multi-omics integration report.

Frequently Asked Questions about tooluniverse-multi-omics-integration

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

FAQPage Schema
How do I integrate RNA-seq and proteomics data?

Match common samples across both matrices, map features to gene-level identifiers, then compute Spearman correlation per gene. Typical RNA-protein correlations range from 0.4 to 0.6; genes with |r| below 0.2 are flagged as discordant and may indicate post-transcriptional regulation.

What clustering methods work for multi-omics patient subtyping?

MOFA+ identifies latent factors explaining cross-omics variance, joint NMF performs shared decomposition across omics layers, and SNF fuses similarity networks from heterogeneous data types. MOFA+ is best for separating shared versus omics-specific drivers.

How does methylation affect gene expression in multi-omics analysis?

Promoter methylation typically represses expression, so expect negative Spearman correlations between CpG beta values and gene expression. Genes with r below -0.5 and p below 0.01 are flagged as epigenetically regulated, though exceptions to the repression model exist.

What is the minimum sample size for multi-omics integration?

At least 10 common samples across omics types are required, but 20 or more are recommended for reliable integration. If not all samples have all omics types, use pairwise integration instead of requiring complete intersection.

What are the limitations of multi-omics correlation analysis?

Batch effects across platforms require careful normalization, large datasets demand significant memory, and results need domain expertise for interpretation. Discordant RNA-protein pairs may reflect real post-transcriptional regulation rather than noise.