immune-repertoire-analysis

name	immune-repertoire-analysis
description	ToolUniverse workflow — Immune Repertoire Analysis
source	https://github.com/mims-harvard/ToolUniverse/tree/main/skills/tooluniverse-immune-repertoire-analysis
metadata	null

---

name: tooluniverse-immune-repertoire-analysis description: Comprehensive immune repertoire analysis for T-cell and B-cell receptor sequencing data. Analyze TCR/BCR repertoires to assess clonality, diversity, V(D)J gene usage, CDR3 characteristics, convergence, and predict epitope specificity. Integrate with single-cell data for clonotype-phenotype associations. Use for adaptive immune response profiling, cancer immunotherapy research, vaccine response assessment, autoimmune disease studies, or repertoire diversity analysis in immunology research.

ToolUniverse Immune Repertoire Analysis

Comprehensive skill for analyzing T-cell receptor (TCR) and B-cell receptor (BCR) repertoire sequencing data to characterize adaptive immune responses, clonal expansion, and antigen specificity.

Overview

Adaptive immune receptor repertoire sequencing (AIRR-seq) enables comprehensive profiling of T-cell and B-cell populations through high-throughput sequencing of TCR and BCR variable regions. This skill provides an 8-phase workflow for:

• Clonotype identification and tracking
• Diversity and clonality assessment
• V(D)J gene usage analysis
• CDR3 sequence characterization
• Clonal expansion and convergence detection
• Epitope specificity prediction
• Integration with single-cell phenotyping
• Longitudinal repertoire tracking

Core Workflow

Phase 1: Data Import & Clonotype Definition

Load AIRR-seq Data

import pandas as pd
import numpy as np
from collections import Counter

def load_airr_data(file_path, format='mixcr'):
    """
    Load immune repertoire data from common formats.

    Supported formats:
    - 'mixcr': MiXCR output
    - 'immunoseq': Adaptive Biotechnologies ImmunoSEQ
    - 'airr': AIRR Community Standard
    - '10x': 10x Genomics VDJ output
    """
    if format == 'mixcr':
        # MiXCR clonotypes.txt format
        df = pd.read_csv(file_path, sep='\t')
        
        # Standardize column names
        clonotype_df = pd.DataFrame({
            'cloneId': df.get('cloneId', range(len(df))),
            'count': df.get('cloneCount', df.get('count', 0)),
            'frequency': df.get('cloneFraction', df.get('frequency', 0)),
            'cdr3aa': df.get('aaSeqCDR3', df.get('cdr3', '')),
            'cdr3nt': df.get('nSeqCDR3', ''),
            'v_gene': df.get('allVHitsWithScore', df.get('v_call', '')),
            'j_gene': df.get('allJHitsWithScore', df.get('j_call', '')),
            : df.get(, )  
        })

      == :
        
        df = pd.read_csv(file_path)
        
        
        clonotype_df = df.groupby().agg({
            :  x: .join(x.dropna()),
            :  x: .join(x.dropna()),
            :  x: .join(x.dropna()),
            :  x: .join(x.dropna()),
            :  x: .join(x.dropna()),
            : 
        }).reset_index()
        
        clonotype_df = clonotype_df.rename(columns={
            : ,
            : ,
            : ,
            : 
        })
        
        clonotype_df[] = clonotype_df[] / clonotype_df[].()

      == :
        
        df = pd.read_csv(file_path, sep=)
        
        clonotype_df = pd.DataFrame({
            : df.get(, ((df))),
            : df.get(, ),
            : df.get(, df.get(, ) / df.get(, ).()),
            : df.get(, ),
            : df.get(, ),
            : df.get(, ),
            : df.get(, ),
            : df.get(, )
        })

    
    clonotype_df[] = clonotype_df[]..()
    
     clonotype_df


tcr_data = load_airr_data(, =)
()
()

Define Clonotypes

def define_clonotypes(df, method='cdr3aa'):
    """
    Define clonotypes based on various criteria.

    Methods:
    - 'cdr3aa': Amino acid CDR3 sequence only
    - 'cdr3nt': Nucleotide CDR3 sequence
    - 'vj_cdr3': V gene + J gene + CDR3aa (most common)
    """
    if method == 'cdr3aa':
        df['clonotype'] = df['cdr3aa']
    
    elif method == 'cdr3nt':
        df['clonotype'] = df['cdr3nt']
    
    elif method == 'vj_cdr3':
        # Extract V and J gene families (e.g., TRBV12-3 -> TRBV12)
        df['v_family'] = df['v_gene'].str.extract(r'(TRB[VDJ]\d+)', expand=False)
        df['j_family'] = df['j_gene'].str.extract(r'(TRB[VDJ]\d+)', expand=False)
        
        # Combine V + J + CDR3
        df['clonotype'] = df['v_family'] + '_' + df['j_family'] + '_' + df['cdr3aa']
    
    # Aggregate by clonotype
    clonotype_summary = df.groupby('clonotype').agg({
        'count': 'sum',
        'frequency': 'sum'
    }).reset_index()
    
    clonotype_summary = clonotype_summary.sort_values('count', ascending=False)
    clonotype_summary['rank'] = range(1, (clonotype_summary) + )
    
     clonotype_summary


clonotypes = define_clonotypes(tcr_data, method=)
()

Phase 2: Diversity & Clonality Analysis

Calculate Diversity Metrics

def calculate_diversity(clonotype_counts):
    """
    Calculate diversity metrics for immune repertoire.

    Metrics:
    - Shannon entropy: Overall diversity
    - Simpson index: Probability two random clones are same
    - Inverse Simpson: Effective number of clonotypes
    - Gini coefficient: Inequality in clonotype distribution
    """
    from scipy.stats import entropy
    
    # Normalize to frequencies
    if isinstance(clonotype_counts, pd.Series):
        counts = clonotype_counts.values
    else:
        counts = clonotype_counts
    
    freqs = counts / counts.sum()
    
    # Shannon entropy
    shannon = entropy(freqs, base=2)
    
    # Simpson index (D)
    simpson = np.sum(freqs ** 2)
    
    # Inverse Simpson (1/D) - effective number of clonotypes
    inv_simpson = 1 / simpson if simpson > 0 else 0
    
    # Gini coefficient
    sorted_freqs = np.sort(freqs)
    n = len(freqs)
    cumsum = np.cumsum(sorted_freqs)
    gini = (2 * np.sum((np.arange(1, n+1)) * sorted_freqs)) / (n * cumsum[-1]) - (n + 1) / n
    
    # Richness (number of unique clonotypes)
    richness = len(counts)
    
    # Clonality (1 - Pielou's evenness)
    max_entropy = np.log2(richness)
    evenness = shannon / max_entropy if max_entropy > 0 else 0
    clonality = 1 - evenness
    
    return {
        : richness,
        : shannon,
        : simpson,
        : inv_simpson,
        : gini,
        : evenness,
        : clonality
    }


diversity = calculate_diversity(clonotypes[])
()
 metric, value  diversity.items():
    ()

Rarefaction Analysis

def rarefaction_curve(df, n_samples=100, n_boots=10):
    """
    Generate rarefaction curve to assess sampling depth.
    
    Shows how clonotype richness increases with sequencing depth.
    """
    total_reads = df['count'].sum()
    sample_sizes = np.linspace(1000, total_reads, n_samples)
    
    richness_curves = []
    
    for _ in range(n_boots):
        richness_at_depth = []
        
        for sample_size in sample_sizes:
            # Sample reads according to clonotype frequencies
            sampled = np.random.choice(
                df.index,
                size=int(sample_size),
                p=df['frequency'].values,
                replace=True
            )
            
            # Count unique clonotypes
            unique_clonotypes = len(set(sampled))
            richness_at_depth.append(unique_clonotypes)
        
        richness_curves.append(richness_at_depth)
    
    # Calculate mean and std
    mean_richness = np.mean(richness_curves, axis=0)
    std_richness = np.std(richness_curves, axis=0)
    
    return sample_sizes, mean_richness, std_richness

# Generate rarefaction curve
sample_sizes, mean_rich, std_rich = rarefaction_curve(clonotypes)

import matplotlib.pyplot as plt
plt.figure(figsize=(8, 5))
plt.plot(sample_sizes, mean_rich, 'b-', label='Mean richness')
plt.fill_between(sample_sizes, mean_rich - std_rich, mean_rich + std_rich, alpha=0.3)
plt.xlabel('Sequencing Depth (reads)')
plt.ylabel('Clonotype Richness')
plt.title()
plt.legend()
plt.savefig(, dpi=)

Phase 3: V(D)J Gene Usage Analysis

Analyze V and J Gene Usage

def analyze_vdj_usage(df):
    """
    Analyze V(D)J gene usage patterns.
    """
    # Extract gene families
    df['v_family'] = df['v_gene'].str.extract(r'(TRB[VDJ]\d+)', expand=False)
    df['j_family'] = df['j_gene'].str.extract(r'(TRB[VDJ]\d+)', expand=False)
    
    # V gene usage (weighted by count)
    v_usage = df.groupby('v_family')['count'].sum().sort_values(ascending=False)
    v_usage_freq = v_usage / v_usage.sum()
    
    # J gene usage
    j_usage = df.groupby('j_family')['count'].sum().sort_values(ascending=False)
    j_usage_freq = j_usage / j_usage.sum()
    
    # V-J pairing
    vj_pairs = df.groupby(['v_family', 'j_family'])['count'].sum().reset_index()
    vj_pairs['frequency'] = vj_pairs['count'] / vj_pairs['count'].sum()
    vj_pairs = vj_pairs.sort_values('count', ascending=False)
    
    return {
        'v_usage': v_usage_freq,
        'j_usage': j_usage_freq,
        'vj_pairs': vj_pairs
    }

# Analyze V(D)J usage
vdj_usage = analyze_vdj_usage(tcr_data)

print("Top 10 V genes:")
(vdj_usage[].head())

()
(vdj_usage[].head())

()
(vdj_usage[].head())

Statistical Testing for Biased Usage

def test_vdj_bias(observed_usage, expected_frequencies=None):
    """
    Test whether V(D)J gene usage deviates from expected (uniform or reference).
    
    Uses chi-square test.
    """
    from scipy.stats import chisquare
    
    observed = observed_usage.values
    
    if expected_frequencies is None:
        # Assume uniform distribution
        expected = np.ones(len(observed)) / len(observed) * observed.sum()
    else:
        # Use provided reference frequencies
        expected = expected_frequencies * observed.sum()
    
    # Chi-square test
    chi2, pvalue = chisquare(observed, f_exp=expected)
    
    return {
        'chi2_statistic': chi2,
        'p_value': pvalue,
        'significant': pvalue < 0.05
    }

# Test for V gene bias
v_bias_test = test_vdj_bias(vdj_usage['v_usage'] * tcr_data['count'].sum())
print(f"V gene usage bias test: chi2={v_bias_test['chi2_statistic']:.2f}, p={v_bias_test['p_value']:.2e}")

Phase 4: CDR3 Sequence Analysis

CDR3 Length Distribution

def analyze_cdr3_length(df):
    """
    Analyze CDR3 length distribution.
    
    Typical TCR CDR3 length: 12-18 amino acids
    Typical BCR CDR3 length: 10-20 amino acids
    """
    # Length distribution (weighted by count)
    length_dist = df.groupby('cdr3_length')['count'].sum().sort_index()
    length_freq = length_dist / length_dist.sum()
    
    # Statistics
    mean_length = (df['cdr3_length'] * df['count']).sum() / df['count'].sum()
    median_length = df['cdr3_length'].median()
    
    return {
        'length_distribution': length_freq,
        'mean_length': mean_length,
        'median_length': median_length
    }

# Analyze CDR3 length
cdr3_analysis = analyze_cdr3_length(tcr_data)
print(f"Mean CDR3 length: {cdr3_analysis['mean_length']:.1f} aa")
print(f"Median CDR3 length: {cdr3_analysis['median_length']:.0f} aa")

# Plot distribution
plt.figure(figsize=(8, 5))
plt.bar(cdr3_analysis['length_distribution'].index, cdr3_analysis['length_distribution'].values)
plt.xlabel('CDR3 Length (amino acids)')
plt.ylabel('Frequency')
plt.title('CDR3 Length Distribution')
plt.savefig('cdr3_length_distribution.png', dpi=300)

Amino Acid Composition

def analyze_cdr3_composition(cdr3_sequences, weights=None):
    """
    Analyze amino acid composition in CDR3 regions.
    """
    from collections import Counter
    
    if weights is None:
        weights = np.ones(len(cdr3_sequences))
    
    # Count amino acids (weighted by clonotype frequency)
    aa_counts = Counter()
    total_aa = 0
    
    for seq, weight in zip(cdr3_sequences, weights):
        for aa in seq:
            aa_counts[aa] += weight
            total_aa += weight
    
    # Convert to frequencies
    aa_freq = {aa: count / total_aa for aa, count in aa_counts.items()}
    aa_freq_df = pd.DataFrame.from_dict(aa_freq, orient='index', columns=['frequency'])
    aa_freq_df = aa_freq_df.sort_values('frequency', ascending=False)
    
    return aa_freq_df

# Analyze amino acid composition
aa_comp = analyze_cdr3_composition(tcr_data['cdr3aa'], weights=tcr_data['count'])
print("Top 10 amino acids in CDR3:")
print(aa_comp.head(10))

Phase 5: Clonal Expansion Detection

Identify Expanded Clonotypes

def detect_expanded_clones(clonotypes, threshold_percentile=95):
    """
    Identify clonally expanded T/B cell populations.
    
    Expanded clonotypes = clones above frequency threshold.
    """
    # Calculate threshold (e.g., 95th percentile)
    threshold = np.percentile(clonotypes['frequency'], threshold_percentile)
    
    # Identify expanded clones
    expanded = clonotypes[clonotypes['frequency'] >= threshold].copy()
    expanded = expanded.sort_values('frequency', ascending=False)
    
    # Calculate expansion metrics
    total_expanded_freq = expanded['frequency'].sum()
    n_expanded = len(expanded)
    
    return {
        'expanded_clonotypes': expanded,
        'n_expanded': n_expanded,
        'expanded_frequency': total_expanded_freq,
        'threshold': threshold
    }

# Detect expanded clones
expansion_result = detect_expanded_clones(clonotypes, threshold_percentile=95)

print(f"Detected {expansion_result['n_expanded']} expanded clonotypes")
print(f"Expanded clones represent {expansion_result['expanded_frequency']*100:.1f}% of repertoire")
print("\nTop 10 expanded clonotypes:")
print(expansion_result['expanded_clonotypes'].head(10))

Longitudinal Clonotype Tracking

def track_clonotypes_longitudinal(timepoint_dataframes, clonotype_col='clonotype'):
    """
    Track clonotype dynamics across multiple timepoints.
    
    Input: List of DataFrames, each representing one timepoint
    """
    all_timepoints = []
    
    for i, df in enumerate(timepoint_dataframes):
        df_copy = df.copy()
        df_copy['timepoint'] = i
        all_timepoints.append(df_copy[[clonotype_col, 'frequency', 'timepoint']])
    
    # Merge all timepoints
    merged = pd.concat(all_timepoints, ignore_index=True)
    
    # Pivot to wide format
    tracking = merged.pivot(index=clonotype_col, columns='timepoint', values='frequency')
    tracking = tracking.fillna(0)  # Absent clonotypes = 0 frequency
    
    # Calculate persistence
    tracking['persistence'] = (tracking > 0).sum(axis=1)
    tracking['mean_frequency'] = tracking.iloc[:, :-1].mean(axis=1)
    tracking['max_frequency'] = tracking.iloc[:, :-1].max(axis=1)
    
    # Sort by persistence and frequency
    tracking = tracking.sort_values(['persistence', 'max_frequency'], ascending=False)
    
    return tracking

# Example: Track clonotypes across 3 timepoints
# timepoints = [tcr_t0, tcr_t1, tcr_t2]
# tracking = track_clonotypes_longitudinal(timepoints)

Phase 6: Convergence & Public Clonotypes

Detect Convergent Recombination

def detect_convergent_recombination(df):
    """
    Identify cases where different nucleotide sequences encode same CDR3 amino acid.
    
    Convergent recombination = same CDR3aa from different CDR3nt sequences.
    """
    # Group by CDR3 amino acid sequence
    convergence = df.groupby('cdr3aa').agg({
        'cdr3nt': lambda x: len(set(x)),  # Number of unique nucleotide sequences
        'count': 'sum',
        'frequency': 'sum'
    }).reset_index()
    
    # Filter for convergent (>1 nucleotide sequence)
    convergent = convergence[convergence['cdr3nt'] > 1].copy()
    convergent = convergent.rename(columns={'cdr3nt': 'n_nucleotide_variants'})
    convergent = convergent.sort_values('n_nucleotide_variants', ascending=False)
    
    return convergent

# Detect convergence
convergent_clones = detect_convergent_recombination(tcr_data)
print(f"Found {len(convergent_clones)} convergent CDR3 sequences")
print("\nTop 10 convergent sequences:")
print(convergent_clones.head(10))

Identify Public (Shared) Clonotypes

def identify_public_clonotypes(sample_dataframes, min_samples=2):
    """
    Identify public (shared) clonotypes present in multiple samples.
    
    Input: List of DataFrames, each representing one sample
    """
    all_samples = []
    
    for i, df in enumerate(sample_dataframes):
        df_copy = df[['clonotype', 'frequency']].copy()
        df_copy['sample_id'] = f'Sample_{i+1}'
        all_samples.append(df_copy)
    
    # Merge all samples
    merged = pd.concat(all_samples, ignore_index=True)
    
    # Count how many samples each clonotype appears in
    public_counts = merged.groupby('clonotype').agg({
        'sample_id': lambda x: len(set(x)),
        'frequency': 'mean'
    }).reset_index()
    
    public_counts = public_counts.rename(columns={'sample_id': 'n_samples'})
    
    # Filter for public clonotypes
    public = public_counts[public_counts['n_samples'] >= min_samples].copy()
    public = public.sort_values(['n_samples', 'frequency'], ascending=False)
    
    return public

# Example: Identify public clonotypes across 5 samples
# samples = [sample1_tcr, sample2_tcr, sample3_tcr, sample4_tcr, sample5_tcr]
# public_clonotypes = identify_public_clonotypes(samples, min_samples=3)

Phase 7: Epitope Prediction & Specificity

Query IEDB for Known Epitopes

def query_epitope_database(cdr3_sequences, organism='human', top_n=10):
    """
    Query IEDB for known T-cell epitopes matching CDR3 sequences.
    """
    from tooluniverse import ToolUniverse
    tu = ToolUniverse()
    
    epitope_matches = {}
    
    for cdr3 in cdr3_sequences[:top_n]:  # Limit to top clonotypes
        # Search IEDB for CDR3 sequence
        result = tu.run_one_function({
            "name": "IEDB_search_tcells",
            "arguments": {
                "receptor": cdr3,
                "organism": organism
            }
        })
        
        if 'data' in result and 'epitopes' in result['data']:
            epitopes = result['data']['epitopes']
            if len(epitopes) > 0:
                epitope_matches[cdr3] = epitopes
    
    return epitope_matches

# Query IEDB for top expanded clonotypes
# top_clones = expansion_result['expanded_clonotypes']['clonotype'].head(10)
# epitope_matches = query_epitope_database(top_clones)

Predict Epitope Specificity with VDJdb

def predict_specificity_vdjdb(cdr3_sequences, chain='TRB'):
    """
    Predict antigen specificity using VDJdb (TCR database).
    
    VDJdb contains TCR sequences with known epitope specificity.
    """
    # Note: ToolUniverse doesn't have VDJdb tool yet
    # This is a placeholder for manual VDJdb query
    
    print("Manual VDJdb query required:")
    print("1. Go to https://vdjdb.cdr3.net/search")
    print("2. Search for CDR3 sequences:")
    for cdr3 in cdr3_sequences[:10]:
        print(f"   - {cdr3}")
    print("3. Check for matches with known epitopes (virus, tumor antigens)")
    
    # Alternative: Use literature search
    from tooluniverse import ToolUniverse
    tu = ToolUniverse()
    
    specificity_results = {}
    
    for cdr3 in cdr3_sequences[:5]:  # Top 5 only
        result = tu.run_one_function({
            "name": "PubMed_search",
            "arguments": {
                "query": f'"{cdr3}" AND (epitope OR antigen OR specificity)',
                "max_results": 10
            }
        })
        
        if 'data' in result and 'papers' in result['data']:
            papers = result[][]
             (papers) > :
                specificity_results[cdr3] = papers
    
     specificity_results

Phase 8: Integration with Single-Cell Data

Link Clonotypes to Cell Phenotypes

def integrate_with_single_cell(vdj_df, gex_adata, barcode_col='barcode'):
    """
    Integrate TCR/BCR clonotypes with single-cell gene expression.
    
    Requires:
    - vdj_df: DataFrame with clonotype info (from 10x VDJ)
    - gex_adata: AnnData object with gene expression (from 10x GEX)
    """
    import scanpy as sc
    
    # Create clonotype mapping
    clonotype_map = dict(zip(vdj_df[barcode_col], vdj_df['clonotype']))
    
    # Add clonotype info to AnnData
    gex_adata.obs['clonotype'] = gex_adata.obs.index.map(clonotype_map)
    gex_adata.obs['has_clonotype'] = ~gex_adata.obs['clonotype'].isna()
    
    # Identify expanded clonotypes
    clonotype_counts = gex_adata.obs['clonotype'].value_counts()
    expanded_clonotypes = clonotype_counts[clonotype_counts > 5].index.tolist()
    
    gex_adata.obs['is_expanded'] = gex_adata.obs['clonotype'].isin(expanded_clonotypes)
    
    # Visualize on UMAP
    sc.pl.umap(gex_adata, color=['clonotype', 'is_expanded'], 
               title=['Clonotype', 'Expanded Clones'])
    
    return gex_adata

# Example integration
# integrated_data = integrate_with_single_cell(tcr_10x, gex_adata)

Clonotype-Phenotype Association

def analyze_clonotype_phenotype(adata, clonotype_col='clonotype', cluster_col='leiden'):
    """
    Analyze association between clonotypes and cell phenotypes/clusters.
    """
    import scanpy as sc
    
    # Get cells with clonotypes
    cells_with_tcr = adata[~adata.obs[clonotype_col].isna()].copy()
    
    # Count clonotypes per cluster
    clonotype_cluster = pd.crosstab(
        cells_with_tcr.obs[clonotype_col],
        cells_with_tcr.obs[cluster_col],
        normalize='index'
    )
    
    # Find cluster-specific clonotypes (>80% cells in one cluster)
    cluster_specific = clonotype_cluster[clonotype_cluster.max(axis=1) > 0.8]
    
    # Get top expanded clonotypes per cluster
    top_per_cluster = {}
    for cluster in clonotype_cluster.columns:
        top_clonotypes = clonotype_cluster[cluster].sort_values(ascending=False).head(5)
        top_per_cluster[cluster] = top_clonotypes.index.tolist()
    
    return {
        'clonotype_cluster_matrix': clonotype_cluster,
        'cluster_specific_clonotypes': cluster_specific,
        'top_clonotypes_per_cluster': top_per_cluster
    }

# Analyze clonotype-phenotype associations
# associations = analyze_clonotype_phenotype(integrated_data)

Advanced Use Cases

Use Case 1: Cancer Immunotherapy Response Analysis

# Compare TCR repertoires before and after immunotherapy

# Load baseline and post-treatment samples
tcr_baseline = load_airr_data("patient_baseline.txt", format='mixcr')
tcr_post = load_airr_data("patient_post_treatment.txt", format='mixcr')

# Define clonotypes
clones_baseline = define_clonotypes(tcr_baseline, method='vj_cdr3')
clones_post = define_clonotypes(tcr_post, method='vj_cdr3')

# Calculate diversity changes
div_baseline = calculate_diversity(clones_baseline['count'])
div_post = calculate_diversity(clones_post['count'])

print(f"Baseline diversity: {div_baseline['shannon_entropy']:.2f}")
print(f"Post-treatment diversity: {div_post['shannon_entropy']:.2f}")
print(f"Change: {div_post['shannon_entropy'] - div_baseline['shannon_entropy']:.2f}")

# Track clonal expansion
expanded_baseline = detect_expanded_clones(clones_baseline)
expanded_post = detect_expanded_clones(clones_post)

# Identify newly expanded clonotypes
new_clones = set(expanded_post['expanded_clonotypes']['clonotype']) - \
             set(expanded_baseline['expanded_clonotypes']['clonotype'])

print(f"Newly expanded clonotypes: {len(new_clones)}")

# Query epitope specificity for newly expanded clones
epitope_matches = query_epitope_database((new_clones)[:])

Use Case 2: Vaccine Response Tracking

# Track TCR repertoire changes after vaccination

timepoints = [
    load_airr_data("pre_vaccine.txt", format='mixcr'),
    load_airr_data("week1_post.txt", format='mixcr'),
    load_airr_data("week4_post.txt", format='mixcr'),
    load_airr_data("week12_post.txt", format='mixcr')
]

# Process each timepoint
clonotype_dfs = [define_clonotypes(df, method='vj_cdr3') for df in timepoints]

# Track longitudinal dynamics
tracking = track_clonotypes_longitudinal(clonotype_dfs)

# Identify persistent vaccine-responding clones
persistent_clones = tracking[tracking['persistence'] == 4]  # Present at all timepoints
print(f"Persistent clonotypes: {len(persistent_clones)}")

# Identify clonotypes that expanded after vaccination
tracking['fold_change'] = tracking.iloc[:, 3] / (tracking.iloc[:, 0] + 1e-6)
vaccine_responders = tracking[tracking['fold_change'] > 10]
print(f"Vaccine-responding clonotypes (>10-fold expansion): {len(vaccine_responders)}")

Use Case 3: Autoimmune Disease Repertoire Analysis

# Compare TCR repertoires between autoimmune patients and healthy controls

# Load data
patient_tcr = load_airr_data("autoimmune_patient.txt", format='mixcr')
control_tcr = load_airr_data("healthy_control.txt", format='mixcr')

# Define clonotypes
patient_clones = define_clonotypes(patient_tcr, method='vj_cdr3')
control_clones = define_clonotypes(control_tcr, method='vj_cdr3')

# Compare diversity
div_patient = calculate_diversity(patient_clones['count'])
div_control = calculate_diversity(control_clones['count'])

print(f"Patient clonality: {div_patient['clonality']:.3f}")
print(f"Control clonality: {div_control['clonality']:.3f}")

# Identify disease-specific clonotypes
patient_specific = set(patient_clones['clonotype']) - set(control_clones['clonotype'])
print(f"Patient-specific clonotypes: {len(patient_specific)}")

# Analyze V(D)J usage bias
vdj_patient = analyze_vdj_usage(patient_tcr)
vdj_control = analyze_vdj_usage(control_tcr)

# Compare V gene usage
v_comparison = pd.DataFrame({
    'patient': vdj_patient['v_usage'],
    'control': vdj_control['v_usage']
}).fillna(0)

v_comparison['fold_change'] = (v_comparison['patient'] + 1e-6) / (v_comparison[] + )
biased_v_genes = v_comparison[v_comparison[] > ]
()

Use Case 4: Single-Cell TCR-seq + RNA-seq Integration

# Integrate TCR clonotypes with T-cell phenotypes

import scanpy as sc

# Load 10x data
tcr_10x = load_airr_data("filtered_contig_annotations.csv", format='10x')
gex_adata = sc.read_10x_h5("filtered_feature_bc_matrix.h5")

# Standard single-cell processing
sc.pp.filter_cells(gex_adata, min_genes=200)
sc.pp.normalize_total(gex_adata, target_sum=1e4)
sc.pp.log1p(gex_adata)
sc.pp.highly_variable_genes(gex_adata, n_top_genes=2000)
sc.pp.pca(gex_adata)
sc.pp.neighbors(gex_adata)
sc.tl.umap(gex_adata)
sc.tl.leiden(gex_adata)

# Integrate TCR data
integrated = integrate_with_single_cell(tcr_10x, gex_adata)

# Analyze clonotype-phenotype associations
associations = analyze_clonotype_phenotype(integrated)

# Identify phenotype of expanded clones
expanded_cells = integrated[integrated.obs['is_expanded']].copy()
sc.pl.umap(expanded_cells, color='leiden', title='Phenotype of Expanded Clones')

# Find marker genes for expanded vs non-expanded
sc.tl.rank_genes_groups(integrated, 'is_expanded', method='wilcoxon')
sc.pl.rank_genes_groups(integrated, n_genes=20)

ToolUniverse Tool Integration

Key Tools Used:

• IEDB_search_tcells - Known T-cell epitopes
• IEDB_search_bcells - Known B-cell epitopes
• PubMed_search - Literature on TCR/BCR specificity
• UniProt_get_protein - Antigen protein information

Integration with Other Skills:

• tooluniverse-single-cell - Single-cell transcriptomics
• tooluniverse-rnaseq-deseq2 - Bulk RNA-seq analysis
• tooluniverse-variant-analysis - Somatic hypermutation analysis (BCR)

Best Practices

1. Sequencing Depth: Aim for 10,000+ unique UMIs per sample for bulk TCR-seq; 500+ for single-cell

2. Technical Replicates: Use biological replicates (n≥3) for statistical comparisons

3. Clonotype Definition: Use V+J+CDR3aa for most analyses (balances specificity and sensitivity)

4. Diversity Metrics: Report multiple metrics (Shannon, Simpson, clonality) for comprehensive assessment

5. Rare Clonotypes: Filter clonotypes with very low frequency (<0.001%) to remove sequencing errors

6. Public Clonotypes: Check VDJdb, McPAS-TCR databases for known antigen specificities

7. CDR3 Length: Flag unusual length distributions (may indicate PCR bias or sequencing issues)

8. V(D)J Annotation: Use high-quality reference databases (IMGT, TRAPeS)

9. Batch Effects: Correct for batch effects when comparing samples from different runs

10. Functional Validation: Validate predicted specificities with tetramer staining or functional assays

Troubleshooting

Problem: Very low diversity (few dominant clonotypes)

• Solution: May indicate clonal expansion (biological) or PCR bias (technical); check sequencing QC

Problem: Unusual CDR3 length distribution

• Solution: Check for PCR amplification bias; verify primer design

Problem: Many non-productive sequences

• Solution: May indicate B-cell repertoire or contamination; filter for productive sequences only

Problem: No matches in epitope databases

• Solution: Most TCR/BCR specificities are unknown; use convergence and public clonotype analysis

Problem: Low integration rate with single-cell GEX

• Solution: Check cell barcodes match; ensure VDJ and GEX libraries from same cells

References

• Dash P, et al. (2017) Quantifiable predictive features define epitope-specific T cell receptor repertoires. Nature
• Glanville J, et al. (2017) Identifying specificity groups in the T cell receptor repertoire. Nature
• Stubbington MJT, et al. (2016) T cell fate and clonality inference from single-cell transcriptomes. Nature Methods
• Vander Heiden JA, et al. (2014) pRESTO: a toolkit for processing high-throughput sequencing raw reads of lymphocyte receptor repertoires. Bioinformatics

Quick Start

# Minimal workflow
from tooluniverse import ToolUniverse

# 1. Load data
tcr_data = load_airr_data("clonotypes.txt", format='mixcr')

# 2. Define clonotypes
clonotypes = define_clonotypes(tcr_data, method='vj_cdr3')

# 3. Calculate diversity
diversity = calculate_diversity(clonotypes['count'])
print(f"Shannon entropy: {diversity['shannon_entropy']:.2f}")

# 4. Detect expanded clones
expansion = detect_expanded_clones(clonotypes)
print(f"Expanded clonotypes: {expansion['n_expanded']}")

# 5. Analyze V(D)J usage
vdj_usage = analyze_vdj_usage(tcr_data)

# 6. Query epitope databases
top_clones = expansion['expanded_clonotypes']['clonotype'].head(10)
epitopes = query_epitope_database(top_clones)