Agent skill · Data & Analytics

bio-multi-omics-mofa-integration

Multi-Omics Factor Analysis (MOFA2) for unsupervised integration of multiple data modalities. Identifies shared and view-specific sources of variation. Use when integrating RNA-seq, proteomics, methylation, or other omics to discover latent factors driving biological variation across modalities.

FreedomIntelligencegithub.com/FreedomIntelligenceGitHub ↗
claude-code
Install
npx skills add FreedomIntelligence/OpenClaw-Medical-Skills --skill bio-multi-omics-mofa-integration --agent claude-code

Same command for any agent — swap --agent for codex, cursor, copilot.

Facts
Files in the skill folder: 3
SKILL.md size: 7 KB
Bundled scripts: none
Path: skills/bio-multi-omics-mofa-integration/SKILL.md
Open the folder on GitHub →
Where it comes from
Stars: 2,909
Language: Python
Read our review of the source →

Weekly change comes from our own snapshots, not the repository page — it measures attention, not adoption.

From the SKILL.md

## Version Compatibility Reference examples tested with: scanpy 1.10+ Before using code patterns, verify installed versions match. If versions differ: - R: `packageVersion('<pkg>')` then `?function_name` to verify parameters If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying. # MOFA2 Integration **"Find shared variation across my omics layers"** → Discover latent factors that capture shared and modality-specific sources of biological variation in an unsupervised manner. - R: `MOFA2::create_mofa()` → `prepare_mofa()` → `run_mofa()` - Python: `mofapy2` for training, `muon` for downstream ## Prepare Multi-Omics Data **Goal:** Load and align multiple omics matrices into a consistent format for MOFA2 input. **Approach:** Read each omics layer, intersect to common samples, transpose to features-by-samples orientation. ```r library(MOFA2) library(MultiAssayExperiment) # Load individual omics matrices (samples x features) rna <- as.matrix(read.csv('rnaseq_matrix.csv', row.names = 1)) protein <- as.matrix(read.csv('proteomics_matrix.csv', row.names = 1)) methylation <- as.matrix(read.c

What's inside
Steps it walks through
  1. Version Compatibility
  2. Prepare Multi-Omics Data
  3. Create and Train MOFA Model
  4. Analyze Factors
  5. Visualize Results
  6. Factor Interpretation
  7. Add Sample Metadata
  8. Multi-Group MOFA
  9. MOFA+ for Single-Cell
  10. Export Results
  11. Related Skills
Ships with 2 files
  • examples/mofa_workflow.R
  • usage-guide.md
More from OpenClaw-Medical-Skills
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About this skill
What does the bio-multi-omics-mofa-integration skill do?

Multi-Omics Factor Analysis (MOFA2) for unsupervised integration of multiple data modalities. Identifies shared and view-specific sources of variation. Use when integrating RNA-seq, proteomics, methylation, or other omics to discover latent factors driving biological variation across modalities.

How do I install it?

Run `npx skills add FreedomIntelligence/OpenClaw-Medical-Skills --skill bio-multi-omics-mofa-integration --agent claude-code` — it drops the skill into your project so the agent can pick it up. Swap the --agent value for codex, cursor or copilot if you use one of those.

Where does this skill come from?

From FreedomIntelligence/OpenClaw-Medical-Skills, a repository with 2,909 stars. We read it straight from the repository tree rather than a submitted listing, so what you see here is what is actually published.

Is a popular skill a good skill?

Not necessarily. Stars measure attention, not adoption — a repository can trend for a week and be abandoned. That is why we show the weekly change from our own snapshots next to the total, instead of a single flattering number.

Keep going