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Bio Experimental Design Sample Size

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Estimates required sample sizes for differential expression, ChIP-seq, methylation, and proteomics studies. Use when budgeting experiments, writing grant proposals, or determining minimum replicates needed to achieve statistical significance for expected effect sizes.

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  • Added September 5, 2026
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SKILL.md
---
name: bio-experimental-design-sample-size
description: Estimates required sample sizes for differential expression, ChIP-seq, methylation, and proteomics studies. Use when budgeting experiments, writing grant proposals, or determining minimum replicates needed to achieve statistical significance for expected effect sizes.
tool_type: r
primary_tool: ssizeRNA
measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes.
allowed-tools:
  - read_file
  - run_shell_command
---

<!--
# COPYRIGHT NOTICE
# This file is part of the "Universal Biomedical Skills" project.
# Copyright (c) 2026 MD BABU MIA, PhD <md.babu.mia@mssm.edu>
# All Rights Reserved.
#
# This code is proprietary and confidential.
# Unauthorized copying of this file, via any medium is strictly prohibited.
#
# Provenance: Authenticated by MD BABU MIA

-->


# Sample Size Estimation

## RNA-seq Sample Size

```r
library(ssizeRNA)

# Estimate sample size for RNA-seq
# m = total genes, m1 = expected DE genes
# fc = fold change, fdr = target FDR
result <- ssizeRNA_single(nGenes = 20000, pi0 = 0.9, m = 200,
                          mu = 10, disp = 0.1, fc = 2,
                          fdr = 0.05, power = 0.8)
result$ssize  # Required n per group
```

## DESeq2-based Estimation

```r
library(DESeq2)

# From pilot data
dds_pilot <- DESeqDataSetFromMatrix(pilot_counts, colData, ~condition)
dds_pilot <- DESeq(dds_pilot)

# Extract dispersion estimates for power calculation
dispersions <- mcols(dds_pilot)$dispGeneEst
median_disp <- median(dispersions, na.rm = TRUE)
# Use median_disp in power calculations
```

## Single-cell Sample Size

```r
library(powsimR)

# Estimate for scRNA-seq
# Accounts for dropout and cell-to-cell variability
params <- estimateParam(pilot_sce)
power <- simulateDE(params, n1 = 100, n2 = 100,
                    p.DE = 0.1, pLFC = 1)
```

## Sample Size by Assay Type

| Assay | Min Recommended | For Small Effects |
|-------|-----------------|-------------------|
| Bulk RNA-seq | 3 | 6-12 |
| scRNA-seq | 3 samples, 1000 cells | 6+ samples |
| ATAC-seq | 2 | 4-6 |
| ChIP-seq | 2 | 3-4 |
| Proteomics | 3 | 6-10 |
| Methylation | 4 | 8-12 |

## Budget Optimization

When resources are limited, prioritize:
1. Biological replicates over technical replicates
2. More samples over deeper sequencing (after ~20M reads for RNA-seq)
3. Balanced designs (equal n per group)

## Related Skills

- experimental-design/power-analysis - Power calculations
- experimental-design/batch-design - Optimal batch assignment
- single-cell/preprocessing - scRNA-seq experimental design


<!-- AUTHOR_SIGNATURE: 9a7f3c2e-MD-BABU-MIA-2026-MSSM-SECURE -->

Files in this skill

  • SKILL.md2.6 KB
  • examples/sample_size_estimation.R3.8 KB
  • usage-guide.md2.1 KB

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