Install
$ agentstack add skill-mannlabs-proteomics-agent-skills-performing-statistical-analysis ✓ scanned · ✓ verified, works with Claude Code, Cursor, and more.
Security review
✓ PassedNo 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
Declared compatibility
Compatibility is declared by the source manifest. End-to-end runtime verification is coming, see below.
We're building live execution health for every listing: tool-call success rate, median latency, uptime, and last-checked timestamps, measured, not self-reported. It isn't live yet, so we don't show numbers we can't stand behind.
How agent discovery & health will work →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.
- Author: MannLabs
- Source: MannLabs/proteomics-agent-skills
- License: Apache-2.0
Install and usage instructions live in the source repository linked above.
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Versions
- v0.1.0 Imported from the upstream source.