Data & ReproBioinformatics & GenomicsFreedomIntelligence/OpenClaw-Medical-SkillsData & Reproduction
BI

bio-multi-omics-mixomics-analysis

Maintainer FreedomIntelligence · Last updated April 1, 2026

Supervised and unsupervised multi-omics integration with mixOmics. Includes sPLS for pairwise integration and DIABLO for multi-block discriminant analysis. Use when performing supervised multi-omics integration or identifying features that discriminate between groups.

OpenClawNanoClawAnalysisReproductionbio-multi-omics-mixomics-analysis🧬 bioinformatics (gptomics bio-* suite)bioinformatics — multi-omics integrationsupervised

Original source

FreedomIntelligence/OpenClaw-Medical-Skills

https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-multi-omics-mixomics-analysis

Maintainer
FreedomIntelligence
License
MIT
Last updated
April 1, 2026

Skill Snapshot

Key Details From SKILL.md

2 min

Key Notes

  • R: mixOmics::block.splsda() (DIABLO), mixOmics::spls() for pairwise integration.
  • Integrate my multi-omics data with supervised analysis" → Identify cross-omics feature signatures that discriminate between groups using sparse PLS and multi-block discriminant analysis. R: mixOmics::block.splsda() (DIABLO), mixOmics::spls() for pairwise integration.
  • X_rna <- as.matrix(read.csv('rnaseq.csv', row.names = 1)) X_protein <- as.matrix(read.csv('proteomics.csv', row.names = 1)) Y <- factor(read.csv('phenotype.csv')$Condition).

Source Doc

Excerpt From SKILL.md

Setup and Data Preparation

Goal: Load and align omics matrices with matching sample labels and phenotype information.

Approach: Read each omics layer and phenotype, then intersect to common samples.

library(mixOmics)

## Ensure matching samples

common <- Reduce(intersect, list(rownames(X_rna), rownames(X_protein)))
X_rna <- X_rna[common, ]
X_protein <- X_protein[common, ]
Y <- Y[match(common, read.csv('phenotype.csv')$Sample)]

Pairwise Integration: sPLS

Goal: Identify correlated features between two omics layers using sparse partial least squares.

Approach: Tune component count, fit sPLS with feature selection (keepX/keepY), and visualize cross-omics correlations.

Use cases

  • Use when performing supervised multi-omics integration or identifying features that discriminate between groups.

Not for

  • Do not rely on this catalog entry alone for installation or maintenance details.

Upstream Related Skills

  • mofa-integration - Unsupervised multi-omics
  • data-harmonization - Preprocess before integration
  • differential-expression/de-results - Single-omics analysis
  • pathway-analysis/go-enrichment - Interpret selected features

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