
Deg Screening Analysis
Use when screening differentially expressed genes from a bulk expression matrix between...
Install
npx skills add aipoch/medical-research-skills --skill deg-screening-analysis -g -a claude-code -y- Repository
- aipoch/medical-research-skills2k
- Category
- Engineering
- Updated
- 2mo ago
- License
- MIT
- Context cost
- Mediumabout 1,943 tokens
- Runs scripts
- No, instructions only
What it does
Use when screening differentially expressed genes from a bulk expression matrix between two user-specified groups, producing DEG tables, a volcano plot, and a clustered heatmap. Triggers include DEG analysis, volcano plot, clustered heatmap, limma-based two-group comparison, and case-vs-control screening. NOT for single-cell RNA-seq, multi-group contrasts, count-model workflows such as DESeq2/edgeR, or non-expression omics data.
Differential Expression Gene Screening Analysis (Volcano Plot & Clustered Heatmap)
When to Use
Use this skill when you need a reproducible two-group DEG workflow on a bulk expression matrix and want:
- a full differential expression table
- a filtered DEG table
- a volcano plot
- a clustered heatmap of top differential genes
Typical requests include:
- compare case vs control samples with limma
- screen upregulated and downregulated genes from a normalized expression matrix
- generate a DEG table with volcano and heatmap outputs from bulk transcriptome data
Out of Scope
Do not use this skill for:
- single-cell RNA-seq workflows
- multi-group contrasts or factorial designs
- count-model pipelines that require
DESeq2oredgeR - batch correction, covariate-adjusted models, or generalized design-matrix consulting
- non-expression omics data
If the request falls outside this scope, stop and hand off to a more appropriate analysis workflow instead of forcing the data through this skill.
Practical Caveats
Diffanalysis.csvcurrently exportsname,logFC,P.value, andP.adj.--p_typecontrols both DEG screening semantics and volcano plot significance semantics.plot/heatmap.pdfis generated only when at least two heatmap genes remain after ranking.- When the result is very sparse, prefer keeping tables and volcano output as the primary artifacts.
