bio-tcr-bcr-analysis-repertoire-visualization
$
npx mdskill add GPTomics/bioSkills/bio-tcr-bcr-analysis-repertoire-visualizationGenerate publication-quality immune repertoire visualizations for research figures.
- Creates circos plots, clone tracking, and diversity graphs from TCR/BCR data.
- Depends on VDJtools, matplotlib, seaborn, and pandas for data processing.
- Selects visualization type based on user request for repertoire comparisons.
- Outputs high-resolution images ready for publication in scientific journals.
SKILL.md
.github/skills/bio-tcr-bcr-analysis-repertoire-visualizationView on GitHub ↗
---
name: bio-tcr-bcr-analysis-repertoire-visualization
description: Create publication-quality visualizations of immune repertoire data including circos plots, clone tracking, diversity plots, and network graphs. Use when generating figures for repertoire comparisons, clonal dynamics, or V(D)J gene usage.
tool_type: mixed
primary_tool: VDJtools
---
## Version Compatibility
Reference examples tested with: MiXCR 4.6+, VDJtools 1.2.1+, ggplot2 3.5+, matplotlib 3.8+, pandas 2.2+, scanpy 1.10+, seaborn 0.13+
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
- CLI: `<tool> --version` then `<tool> --help` to confirm flags
If code throws ImportError, AttributeError, or TypeError, introspect the installed
package and adapt the example to match the actual API rather than retrying.
# Repertoire Visualization
**"Visualize my immune repertoire data"** → Create publication-quality figures for TCR/BCR repertoires including circos plots, V(D)J gene usage heatmaps, diversity plots, and clonal tracking across samples.
- CLI: `vdjtools PlotFancyVJUsage` for circos-style V-J plots
- Python: `matplotlib`/`seaborn` for custom repertoire visualizations
## Circos Plots (V-J Gene Usage)
### VDJtools
```bash
# Generate V-J usage circos plot
vdjtools PlotFancyVJUsage \
-m metadata.txt \
output_dir/
# Generates PDF circos plots showing V-J pairing frequencies
```
### Python with pyCircos
```python
import pandas as pd
import matplotlib.pyplot as plt
from pycircos import Gcircle
def plot_vj_circos(clone_df):
'''Create circos plot of V-J usage'''
# Count V-J pairs
vj_counts = clone_df.groupby(['v_gene', 'j_gene']).size().reset_index(name='count')
# Create circos
circle = Gcircle()
# Add arcs for each V and J gene
v_genes = vj_counts['v_gene'].unique()
j_genes = vj_counts['j_gene'].unique()
# Add sectors and links
# ... (complex setup)
circle.save('vj_circos.pdf')
```
### R with circlize
```r
library(circlize)
plot_vj_circos <- function(clone_df) {
# Prepare adjacency matrix
vj_matrix <- table(clone_df$v_gene, clone_df$j_gene)
# Create circos plot
chordDiagram(
vj_matrix,
transparency = 0.5,
annotationTrack = c("grid", "name")
)
}
```
## Clone Tracking Over Time
```python
import pandas as pd
import matplotlib.pyplot as plt
def plot_clone_tracking(clones_by_time, top_n=10):
'''Track top clones across timepoints'''
# Get top clones by total frequency
total_freq = clones_by_time.groupby('cdr3_aa')['frequency'].sum()
top_clones = total_freq.nlargest(top_n).index
fig, ax = plt.subplots(figsize=(10, 6))
for clone in top_clones:
clone_data = clones_by_time[clones_by_time['cdr3_aa'] == clone]
ax.plot(clone_data['timepoint'], clone_data['frequency'],
marker='o', label=clone[:20])
ax.set_xlabel('Timepoint')
ax.set_ylabel('Clone Frequency')
ax.legend(bbox_to_anchor=(1.05, 1), loc='upper left')
plt.tight_layout()
plt.savefig('clone_tracking.pdf')
```
## Diversity Plots
```python
import matplotlib.pyplot as plt
import seaborn as sns
def plot_diversity_comparison(diversity_df, metric='shannon'):
'''Compare diversity between groups'''
fig, ax = plt.subplots(figsize=(8, 6))
sns.boxplot(
data=diversity_df,
x='condition',
y=metric,
ax=ax
)
sns.stripplot(
data=diversity_df,
x='condition',
y=metric,
color='black',
alpha=0.5,
ax=ax
)
ax.set_ylabel(f'{metric.capitalize()} Diversity')
plt.savefig('diversity_comparison.pdf')
```
## Overlap Heatmap
```python
def plot_overlap_heatmap(overlap_matrix):
'''Plot pairwise repertoire overlap'''
import seaborn as sns
fig, ax = plt.subplots(figsize=(10, 8))
sns.heatmap(
overlap_matrix,
annot=True,
fmt='.2f',
cmap='YlOrRd',
ax=ax
)
ax.set_title('Repertoire Overlap (Jaccard Index)')
plt.tight_layout()
plt.savefig('overlap_heatmap.pdf')
```
## Spectratype Plot
```python
def plot_spectratype(clone_df, group_col=None):
'''Plot CDR3 length distribution'''
fig, ax = plt.subplots(figsize=(10, 6))
clone_df['cdr3_length'] = clone_df['cdr3_nt'].str.len()
if group_col:
for group, data in clone_df.groupby(group_col):
ax.hist(data['cdr3_length'], bins=range(20, 80, 3),
alpha=0.5, label=group, density=True)
ax.legend()
else:
ax.hist(clone_df['cdr3_length'], bins=range(20, 80, 3))
ax.set_xlabel('CDR3 Length (nt)')
ax.set_ylabel('Density')
ax.set_title('CDR3 Length Distribution (Spectratype)')
plt.savefig('spectratype.pdf')
```
## Clonotype Network
```python
import networkx as nx
def plot_clone_network(clone_df, similarity_threshold=0.8):
'''Create network of similar clonotypes'''
from Levenshtein import ratio
G = nx.Graph()
clones = clone_df['cdr3_aa'].unique()
# Add nodes
for clone in clones:
freq = clone_df[clone_df['cdr3_aa'] == clone]['frequency'].sum()
G.add_node(clone, size=freq)
# Add edges for similar clones
for i, c1 in enumerate(clones):
for c2 in clones[i+1:]:
sim = ratio(c1, c2)
if sim >= similarity_threshold:
G.add_edge(c1, c2, weight=sim)
# Draw network
fig, ax = plt.subplots(figsize=(12, 12))
pos = nx.spring_layout(G)
sizes = [G.nodes[n]['size'] * 1000 for n in G.nodes()]
nx.draw(G, pos, node_size=sizes, with_labels=False, ax=ax)
plt.savefig('clone_network.pdf')
```
## Related Skills
- vdjtools-analysis - Generate input data
- mixcr-analysis - Generate clonotype tables
- data-visualization/ggplot2-fundamentals - General plotting concepts
More from GPTomics/bioSkills
- bio-admet-predictionPredicts ADMET properties using ADMETlab 3.0 API or DeepChem models. Estimates bioavailability, CYP inhibition, hERG liability, and 119 toxicity endpoints with uncertainty quantification. Filters for PAINS and other structural alerts. Use when filtering compounds for drug-likeness or prioritizing leads by predicted safety.
- bio-alignment-amplicon-clippingTrim PCR primers from aligned reads in amplicon-panel BAMs using samtools ampliconclip. Use when processing SARS-CoV-2 ARTIC, hereditary cancer panels, ctDNA hot-spot panels, or any amplicon assay where primer-derived bases would falsely confirm reference at primer footprints.
- bio-alignment-filteringFilter alignments by flags, mapping quality, and regions using samtools view and pysam. Use when extracting specific reads, removing low-quality alignments, or subsetting to target regions.
- bio-alignment-indexingCreate and use BAI/CSI indices for BAM/CRAM files using samtools and pysam. Use when enabling random access to alignment files or fetching specific genomic regions.
- bio-alignment-ioRead, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.
- bio-alignment-msa-parsingParse and analyze multiple sequence alignments using Biopython. Extract sequences, identify conserved regions, analyze gaps, work with annotations, and manipulate alignment data for downstream analysis. Use when parsing or manipulating multiple sequence alignments.
- bio-alignment-msa-statisticsCalculate alignment statistics including sequence identity, conservation scores, substitution matrices, and similarity metrics. Use when comparing alignment quality, measuring sequence divergence, and analyzing evolutionary patterns.
- bio-alignment-multiplePerform multiple sequence alignment using MAFFT, MUSCLE5, ClustalOmega, or T-Coffee. Guides tool and algorithm selection based on dataset size, sequence divergence, and downstream application. Use when aligning three or more homologous sequences for phylogenetics, conservation analysis, or evolutionary studies.
- bio-alignment-pairwisePerform pairwise sequence alignment using Biopython Bio.Align.PairwiseAligner. Use when comparing two sequences, finding optimal alignments, scoring similarity, and identifying local or global matches between DNA, RNA, or protein sequences.
- bio-alignment-sortingSort alignment files by coordinate or read name using samtools and pysam. Use when preparing BAM files for indexing, variant calling, or paired-end analysis.