install
source · Clone the upstream repo
git clone https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills
Claude Code · Install into ~/.claude/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.claude/skills && cp -r "$T/skills/bio-experimental-design-sample-size" ~/.claude/skills/freedomintelligence-openclaw-medical-skills-bio-experimental-design-sample-size && rm -rf "$T"
OpenClaw · Install into ~/.openclaw/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.openclaw/skills && cp -r "$T/skills/bio-experimental-design-sample-size" ~/.openclaw/skills/freedomintelligence-openclaw-medical-skills-bio-experimental-design-sample-size && rm -rf "$T"
manifest:
skills/bio-experimental-design-sample-size/SKILL.mdsource content
<!--
# 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
-->
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
Sample Size Estimation
RNA-seq Sample Size
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$ssize # Required n per group
DESeq2-based Estimation
library(DESeq2) # From pilot data dds_pilot <- DESeqDataSetFromMatrix(pilot_counts, colData, ~condition) dds_pilot <- DESeq(dds_pilot) # Extract dispersion estimates for power calculation dispersions <- mcols(dds_pilot)$dispGeneEst median_disp <- median(dispersions, na.rm = TRUE) # Use median_disp in power calculations
Single-cell Sample Size
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:
- Biological replicates over technical replicates
- More samples over deeper sequencing (after ~20M reads for RNA-seq)
- 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