# Bio Experimental Design Multiple Testing

> Applies multiple testing correction methods including FDR, Bonferroni, and q-value for genomics data. Use when filtering differential expression results, setting significance thresholds, or choosing between correction methods for different study designs. Use when this capability is needed.

- Skill: `tomevault-io/bio-experimental-design-multiple-testing` (Agent Skill, multi-file: 2 files)
- Install (CLI): `npx skillmds@latest add tomevault-io/bio-experimental-design-multiple-testing`
- Raw SKILL.md: https://api.skillmd.com/api/skills/tomevault-io/bio-experimental-design-multiple-testing/raw
- Safety review: pending
- Works with: Claude Code, Claude.ai, OpenAI Codex
- Category: Coding & Dev Tools
- Author: tomevault-io (https://skillmd.com/u/tomevault-io)
- Updated: 2026-09-17
- Page: https://skillmd.com/skills/tomevault-io/bio-experimental-design-multiple-testing

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## Version Compatibility

Reference examples tested with: R stats (base), statsmodels 0.14+

Before using code patterns, verify installed versions match. If versions differ:
- Python: `pip show <package>` then `help(module.function)` to check signatures
- 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.

# Multiple Testing Correction

**"Correct p-values for multiple testing"** → Adjust raw p-values from thousands of simultaneous tests to control false discovery rate or family-wise error rate.
- R: `p.adjust(pvalues, method = 'BH')`, `qvalue::qvalue()`
- Python: `statsmodels.stats.multitest.multipletests()`

## The Problem

Testing 20,000 genes at p < 0.05 yields ~1,000 false positives by chance. Correction is essential.

## Common Methods

### Bonferroni (Most Conservative)

```r
# Strict family-wise error rate control
p_adj <- p.adjust(pvalues, method = 'bonferroni')
# Threshold: alpha / n_tests
# Use for: small gene sets, confirmatory studies
```

### Benjamini-Hochberg FDR (Standard)

```r
# Controls false discovery rate
p_adj <- p.adjust(pvalues, method = 'BH')
# Most common for genomics
# FDR 0.05 = expect 5% of significant results to be false
```

### q-value (Recommended for Large-Scale)

**Goal:** Estimate the false discovery rate for each gene in a genome-wide test while maximizing detection power by estimating the proportion of true nulls.

**Approach:** Fit the q-value model to the p-value distribution, which estimates pi0 (fraction of true null hypotheses) and converts each p-value to a q-value representing the minimum FDR at which that gene would be called significant.

```r
library(qvalue)
qobj <- qvalue(pvalues)
qvalues <- qobj$qvalues
pi0 <- qobj$pi0  # Estimated proportion of true nulls

# q-value directly estimates FDR for each gene
# More powerful than BH when many true positives exist
```

## Method Selection Guide

| Scenario | Recommended Method | Threshold |
|----------|-------------------|-----------|
| Genome-wide DE | BH or q-value | FDR < 0.05 |
| Candidate genes | Bonferroni | p < 0.05/n |
| Exploratory | BH | FDR < 0.10 |
| Validation study | Bonferroni | p < 0.05/n |
| GWAS | Bonferroni | p < 5e-8 |

## Python Equivalent

```python
from statsmodels.stats.multitest import multipletests

# Benjamini-Hochberg
rejected, pvals_corrected, _, _ = multipletests(pvalues, method='fdr_bh')

# Bonferroni
rejected, pvals_corrected, _, _ = multipletests(pvalues, method='bonferroni')
```

## Interpreting Results

- **FDR 0.05**: Among genes called significant, ~5% are false positives
- **FDR 0.01**: More stringent, fewer false positives but more false negatives
- **padj vs qvalue**: Both estimate FDR; q-value is slightly more powerful

## Related Skills

- differential-expression/de-results - Applying corrections to DE output
- population-genetics/association-testing - GWAS significance thresholds
- pathway-analysis/go-enrichment - Correcting enrichment p-values

---
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<!-- tomevault:4.0:skill_md:2026-04-11 -->