222 Document F588feda

PyDESeq2 Workflow Guide

This document provides detailed step-by-step workflows for common PyDESeq2 analysis patterns.

Table of Contents

1. Complete Differential Expression Analysis
2. Data Loading and Preparation
3. Single-Factor Analysis
4. Multi-Factor Analysis
5. Result Export and Visualization
6. Common Patterns and Best Practices
7. Troubleshooting

Complete Differential Expression Analysis

Overview

A standard PyDESeq2 analysis consists of 12 main steps across two phases:

Phase 1: Read Counts Modeling (Steps 1-7)

• Normalization and dispersion estimation
• Log fold-change fitting
• Outlier detection

Phase 2: Statistical Analysis (Steps 8-12)

• Wald testing
• Multiple testing correction
• Optional LFC shrinkage

Full Workflow Code

import pandas as pd
from pydeseq2.dds import DeseqDataSet
from pydeseq2.ds import DeseqStats

# Load data
counts_df = pd.read_csv("counts.csv", index_col=0).T  # Transpose if needed
metadata = pd.read_csv("metadata.csv", index_col=0)

# Filter low-count genes
genes_to_keep = counts_df.columns[counts_df.sum(axis=0) >= 10]
counts_df = counts_df[genes_to_keep]

# Remove samples with missing metadata
samples_to_keep = ~metadata.condition.isna()
counts_df = counts_df.loc[samples_to_keep]
metadata = metadata.loc[samples_to_keep]

# Initialize DeseqDataSet
dds = DeseqDataSet(
    counts=counts_df,
    metadata=metadata,
    design="~condition",
    refit_cooks=True
)

# Run normalization and fitting
dds.deseq2()

# Perform statistical testing
ds = DeseqStats(
    dds,
    contrast=["condition", "treated", "control"],
    alpha=0.05,
    cooks_filter=True,
    independent_filter=True
)
ds.summary()

# Optional: Apply LFC shrinkage for visualization
ds.lfc_shrink()

# Access results
results = ds.results_df
print(results.head())

Data Loading and Preparation

Loading CSV Files

Count data typically comes in genes × samples format but needs to be transposed:

import pandas as pd

# Load count matrix (genes × samples)
counts_df = pd.read_csv("counts.csv", index_col=0)

# Transpose to samples × genes
counts_df = counts_df.T

# Load metadata (already in samples × variables format)
metadata = pd.read_csv("metadata.csv", index_col=0)

Loading from Other Formats

From TSV:

counts_df = pd.read_csv("counts.tsv", sep="\t", index_col=0).T
metadata = pd.read_csv("metadata.tsv", sep="\t", index_col=0)

From saved pickle:

import pickle

with open("counts.pkl", "rb") as f:
    counts_df = pickle.load(f)

with open("metadata.pkl", "rb") as f:
    metadata = pickle.load(f)

From AnnData:

import anndata as ad

adata = ad.read_h5ad("data.h5ad")
counts_df = pd.DataFrame(
    adata.X,
    index=adata.obs_names,
    columns=adata.var_names
)
metadata = adata.obs

Data Filtering

Filter genes with low counts:

# Remove genes with fewer than 10 total reads
genes_to_keep = counts_df.columns[counts_df.sum(axis=0) >= 10]
counts_df = counts_df[genes_to_keep]

Filter samples with missing metadata:

# Remove samples where 'condition' column is NA
samples_to_keep = ~metadata.condition.isna()
counts_df = counts_df.loc[samples_to_keep]
metadata = metadata.loc[samples_to_keep]

Filter by multiple criteria:

# Keep only samples that meet all criteria
mask = (
    ~metadata.condition.isna() &
    (metadata.batch.isin(["batch1", "batch2"])) &
    (metadata.age >= 18)
)
counts_df = counts_df.loc[mask]
metadata = metadata.loc[mask]

Data Validation

Check data structure:

print(f"Counts shape: {counts_df.shape}")  # Should be (samples, genes)
print(f"Metadata shape: {metadata.shape}")  # Should be (samples, variables)
print(f"Indices match: {all(counts_df.index == metadata.index)}")

# Check for negative values
assert (counts_df >= 0).all().all(), "Counts must be non-negative"

# Check for non-integer values
assert counts_df.applymap(lambda x: x == int(x)).all().all(), "Counts must be integers"

Single-Factor Analysis

Simple Two-Group Comparison

Compare treated vs control samples:

from pydeseq2.dds import DeseqDataSet
from pydeseq2.ds import DeseqStats

# Design: model expression as a function of condition
dds = DeseqDataSet(
    counts=counts_df,
    metadata=metadata,
    design="~condition"
)

dds.deseq2()

# Test treated vs control
ds = DeseqStats(
    dds,
    contrast=["condition", "treated", "control"]
)
ds.summary()

# Results
results = ds.results_df
significant = results[results.padj < 0.05]
print(f"Found {len(significant)} significant genes")

Multiple Pairwise Comparisons

When comparing multiple groups:

# Test each treatment vs control
treatments = ["treated_A", "treated_B", "treated_C"]
all_results = {}

for treatment in treatments:
    ds = DeseqStats(
        dds,
        contrast=["condition", treatment, "control"]
    )
    ds.summary()
    all_results[treatment] = ds.results_df

# Compare results across treatments
for name, results in all_results.items():
    sig = results[results.padj < 0.05]
    print(f"{name}: {len(sig)} significant genes")

Multi-Factor Analysis

Two-Factor Design

Account for batch effects while testing condition:

# Design includes both batch and condition
dds = DeseqDataSet(
    counts=counts_df,
    metadata=metadata,
    design="~batch + condition"
)

dds.deseq2()

# Test condition effect while controlling for batch
ds = DeseqStats(
    dds,
    contrast=["condition", "treated", "control"]
)
ds.summary()

Interaction Effects

Test whether treatment effect differs between groups:

# Design includes interaction term
dds = DeseqDataSet(
    counts=counts_df,
    metadata=metadata,
    design="~group + condition + group:condition"
)

dds.deseq2()

# Test the interaction term
ds = DeseqStats(dds, contrast=["group:condition", ...])
ds.summary()

Continuous Covariates

Include continuous variables like age:

# Ensure age is numeric in metadata
metadata["age"] = pd.to_numeric(metadata["age"])

dds = DeseqDataSet(
    counts=counts_df,
    metadata=metadata,
    design="~age + condition"
)

dds.deseq2()

Result Export and Visualization

Saving Results

Export as CSV:

# Save statistical results
ds.results_df.to_csv("deseq2_results.csv")

# Save significant genes only
significant = ds.results_df[ds.results_df.padj < 0.05]
significant.to_csv("significant_genes.csv")

# Save with sorted results
sorted_results = ds.results_df.sort_values("padj")
sorted_results.to_csv("sorted_results.csv")

Save DeseqDataSet:

import pickle

# Save as AnnData for later use
with open("dds_result.pkl", "wb") as f:
    pickle.dump(dds.to_picklable_anndata(), f)

Load saved results:

# Load results
results = pd.read_csv("deseq2_results.csv", index_col=0)

# Load AnnData
with open("dds_result.pkl", "rb") as f:
    adata = pickle.load(f)

Basic Visualization

Volcano plot:

import matplotlib.pyplot as plt
import numpy as np

results = ds.results_df.copy()
results["-log10(padj)"] = -np.log10(results.padj)

# Plot
plt.figure(figsize=(10, 6))
plt.scatter(
    results.log2FoldChange,
    results["-log10(padj)"],
    alpha=0.5,
    s=10
)
plt.axhline(-np.log10(0.05), color='red', linestyle='--', label='padj=0.05')
plt.axvline(1, color='gray', linestyle='--')
plt.axvline(-1, color='gray', linestyle='--')
plt.xlabel("Log2 Fold Change")
plt.ylabel("-Log10(Adjusted P-value)")
plt.title("Volcano Plot")
plt.legend()
plt.savefig("volcano_plot.png", dpi=300)

MA plot:

plt.figure(figsize=(10, 6))
plt.scatter(
    np.log10(results.baseMean + 1),
    results.log2FoldChange,
    alpha=0.5,
    s=10,
    c=(results.padj < 0.05),
    cmap='bwr'
)
plt.xlabel("Log10(Base Mean + 1)")
plt.ylabel("Log2 Fold Change")
plt.title("MA Plot")
plt.savefig("ma_plot.png", dpi=300)

Common Patterns and Best Practices

1. Data Preprocessing Checklist

Before running PyDESeq2:

• ✓ Ensure counts are non-negative integers
• ✓ Verify samples × genes orientation
• ✓ Check that sample names match between counts and metadata
• ✓ Remove or handle missing metadata values
• ✓ Filter low-count genes (typically < 10 total reads)
• ✓ Verify experimental factors are properly encoded

2. Design Formula Best Practices

Order matters: Put adjustment variables before the variable of interest

# Correct: control for batch, test condition
design = "~batch + condition"

# Less ideal: condition listed first
design = "~condition + batch"

Use categorical for discrete variables:

# Ensure proper data types
metadata["condition"] = metadata["condition"].astype("category")
metadata["batch"] = metadata["batch"].astype("category")

3. Statistical Testing Guidelines

Set appropriate alpha:

# Standard significance threshold
ds = DeseqStats(dds, alpha=0.05)

# More stringent for exploratory analysis
ds = DeseqStats(dds, alpha=0.01)

Use independent filtering:

# Recommended: filter low-power tests
ds = DeseqStats(dds, independent_filter=True)

# Only disable if you have specific reasons
ds = DeseqStats(dds, independent_filter=False)

4. LFC Shrinkage

When to use:

• For visualization (volcano plots, heatmaps)
• For ranking genes by effect size
• When prioritizing genes for follow-up

When NOT to use:

• For reporting statistical significance (use unshrunken p-values)
• For gene set enrichment analysis (typically uses unshrunken values)

# Save both versions
ds.results_df.to_csv("results_unshrunken.csv")
ds.lfc_shrink()
ds.results_df.to_csv("results_shrunken.csv")

5. Memory Management

For large datasets:

# Use parallel processing
dds = DeseqDataSet(
    counts=counts_df,
    metadata=metadata,
    design="~condition",
    n_cpus=4  # Adjust based on available cores
)

# Process in batches if needed
# (split genes into chunks, analyze separately, combine results)

Troubleshooting

Error: Index mismatch between counts and metadata

Problem: Sample names don't match

KeyError: Sample names in counts and metadata don't match

Solution:

# Check indices
print("Counts samples:", counts_df.index.tolist())
print("Metadata samples:", metadata.index.tolist())

# Align if needed
common_samples = counts_df.index.intersection(metadata.index)
counts_df = counts_df.loc[common_samples]
metadata = metadata.loc[common_samples]

Error: All genes have zero counts

Problem: Data might need transposition

ValueError: All genes have zero total counts

Solution:

# Check data orientation
print(f"Counts shape: {counts_df.shape}")

# If genes > samples, likely needs transpose
if counts_df.shape[1] < counts_df.shape[0]:
    counts_df = counts_df.T

Warning: Many genes filtered out

Problem: Too many low-count genes removed

Check:

# See distribution of gene counts
print(counts_df.sum(axis=0).describe())

# Visualize
import matplotlib.pyplot as plt
plt.hist(counts_df.sum(axis=0), bins=50, log=True)
plt.xlabel("Total counts per gene")
plt.ylabel("Frequency")
plt.show()

Adjust filtering if needed:

# Try lower threshold
genes_to_keep = counts_df.columns[counts_df.sum(axis=0) >= 5]

Error: Design matrix is not full rank

Problem: Confounded design (e.g., all treated samples in one batch)

Solution:

# Check design confounding
print(pd.crosstab(metadata.condition, metadata.batch))

# Either remove confounded variable or add interaction term
design = "~condition"  # Drop batch
# OR
design = "~condition + batch + condition:batch"  # Add interaction

Issue: No significant genes found

Possible causes:

1. Small effect sizes
2. High biological variability
3. Insufficient sample size
4. Technical issues (batch effects, outliers)

Diagnostics:

# Check dispersion estimates
import matplotlib.pyplot as plt
dispersions = dds.varm["dispersions"]
plt.hist(dispersions, bins=50)
plt.xlabel("Dispersion")
plt.ylabel("Frequency")
plt.show()

# Check size factors (should be close to 1)
print("Size factors:", dds.obsm["size_factors"])

# Look at top genes even if not significant
top_genes = ds.results_df.nsmallest(20, "pvalue")
print(top_genes)

Memory errors on large datasets

Solutions:

# 1. Use fewer CPUs (paradoxically can help)
dds = DeseqDataSet(..., n_cpus=1)

# 2. Filter more aggressively
genes_to_keep = counts_df.columns[counts_df.sum(axis=0) >= 20]

# 3. Process in batches
# Split analysis by gene subsets and combine results