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SKILL verified Apache-2.0 Self-run

Performing Statistical Analysis

skill-mannlabs-proteomics-agent-skills-performing-statistical-analysis · by MannLabs

Perform differential expression analysis on preprocessed proteomics data. Use this when performing finding testing (t-tests, ANOVA) to identify regulated proteins, and multiple testing correction (FDR). Generates standard visualizations like Volcano plots.

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Install

$ agentstack add skill-mannlabs-proteomics-agent-skills-performing-statistical-analysis

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Security review

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No issues found. Passed automated security review. · v0.1.0 How review works →

  • Prompt-injection patterns
  • Secret / credential exfiltration
  • Dangerous shell & filesystem operations
  • Untrusted network calls
  • Known-malicious package signatures

What it can access

  • Network access No
  • Filesystem access No
  • Shell / process execution No
  • Environment & secrets No
  • Dynamic code execution No

From automated source analysis of v0.1.0. “Used” means the capability is present in the source — more access means more to trust, not that it’s unsafe.

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Reliability & compatibility

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About

Performing Proteomics Statistical Analysis

The goal of Differential Expression Analysis (DEA) is to identify proteins that change significantly between conditions.

Context

Experimental conditions

  • Pairwise (2 Groups): Explicitly define "Control" vs. "Treatment"
  • Multi-Group (>2 Groups):
  • Reference-based: Compare every condition against a universal control (e.g., Drug_A vs Ctrl, Drug_B vs Ctrl).
  • All-vs-All: Compare every permutation (e.g., Drug_A vs Drug_B).
  • Global: Use ANOVA to detect if any change exists across groups.

Statistical models

  • t-test: The default for pairwise comparisons. With small sample sizes (typically n 2 Groups: Select Strategy A (ANOVA for global differences) or Strategy B (Specific Pairwise Contrasts).

Step 2: Run a statistical model

  • Pairwise: t-test. Input: Log2-transformed intensities.
  • Multi-group global: One-way ANOVA.

Output: Calculate log2foldchange and raw p_value.

Step 3: Apply Multiple Testing Correction

Method: Apply Benjamini-Hochberg (BH) to raw p-values. Result: Generate a q_value (FDR-adjusted p-value) column.

Step 4: Filter for regulated proteins

Mark proteins as "Significant" (True/False) based on:

  • q_value 1 (2-fold change).

Step 5: Create a Volcano plot

Scatter plot of log2foldchange (x-axis) vs. -Log10 q-value (y-axis). Color significant points.

Hints - Too many significant hits: The cutoff is too loose. Increase log2foldchange threshold or use a stricter FDR (0.01).

Step 6: Create a Heatmap

  • Data: Subset to "Significant" proteins.
  • Scaling: Z-score normalize per feature (here: protein).
  • Clustering: Hierarchical clustering on rows=samples and columns=proteins. Validates if replicates cluster together.

Step 7: Export results

Save table results_statistical_analysis.tsv with columns: protein_group, gene_name, log2_fold_change, p_value, -log10_pvalue, q_value, is_significant.

Source & license

This open-source skill is cataloged on AgentStack and links to its original source — we do not rehost the code.

Install and usage instructions live in the source repository linked above.

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Versions

  • v0.1.0 Imported from the upstream source.