--> --- name: bio-hi-c-analysis-compartment-analysis description: Detect A/B compartments from Hi-C data using cooltools and eigenvector decomposition. Identify active (A) and inactive (B) chromatin compartments from contact matrices. Use when identifying A/B compartments from Hi-C data. tool_type: python primary_tool: cooltools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools: - read_file - run_shell_command --- Detect A/B compartment...
Scanned 9/7/2026
Install to Claude Code
npx -y skills add mdbabumiamssm/LLMs-Universal-Life-Science-and-Clinical-Skills- --skill compartment-analysis --agent claude-codeInstalls into .claude/skills of the current project.
Are you the author of Compartment Analysis?
Add the live security badge to your README — it updates automatically with every re-scan.
[](https://www.skillsdirectory.com/skills/mdbabumiamssm-compartment-analysis)More formats (shields.io, HTML) on the badges page.
<!--
# 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-hi-c-analysis-compartment-analysis
description: Detect A/B compartments from Hi-C data using cooltools and eigenvector decomposition. Identify active (A) and inactive (B) chromatin compartments from contact matrices. Use when identifying A/B compartments from Hi-C data.
tool_type: python
primary_tool: cooltools
measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes.
allowed-tools:
- read_file
- run_shell_command
---
# Compartment Analysis
Detect A/B compartments from Hi-C contact matrices.
## Required Imports
```python
import cooler
import cooltools
import cooltools.lib.plotting
import numpy as np
import pandas as pd
import matplotlib.pyplot as plt
import bioframe
```
## Compute Compartment Eigenvectors
```python
clr = cooler.Cooler('matrix.mcool::resolutions/100000')
# Get reference genome info
view_df = bioframe.make_viewframe(clr.chromsizes)
# Compute expected values first
expected = cooltools.expected_cis(clr, view_df=view_df, ignore_diags=2)
# Compute eigenvector decomposition (compartments)
eigenvector_track = cooltools.eigs_cis(
clr,
view_df=view_df,
phasing_track=None, # Or provide GC content track
n_eigs=3,
)
# Results are returned as a tuple (eigenvalues, eigenvectors)
eigenvalues, eigenvectors = eigenvector_track
print(f'Eigenvalues shape: {eigenvalues.shape}')
print(eigenvectors.head())
```
## Use GC Content for Phasing
```python
# GC content helps orient A/B compartments correctly
# (A compartments typically have higher GC)
# Fetch GC content
gc_track = bioframe.frac_gc(
bioframe.make_viewframe(clr.chromsizes),
bioframe.load_fasta('genome.fa'),
)
# Compute eigenvectors with GC phasing
eigenvalues, eigenvectors = cooltools.eigs_cis(
clr,
view_df=view_df,
phasing_track=gc_track,
n_eigs=1,
)
```
## Extract Compartment Calls
```python
# E1 (first eigenvector) defines compartments
# Positive = A (active), Negative = B (inactive)
eigenvectors['compartment'] = np.where(eigenvectors['E1'] > 0, 'A', 'B')
print(eigenvectors[['chrom', 'start', 'end', 'E1', 'compartment']].head(20))
# Count compartments
print(eigenvectors['compartment'].value_counts())
```
## Compartment Strength (Saddle Plot)
```python
# Compute saddle plot to quantify compartmentalization strength
saddle_data = cooltools.saddle(
clr,
expected=expected,
eigenvector_track=eigenvectors,
view_df=view_df,
n_bins=50,
vrange=(-0.5, 0.5),
)
# saddle_data contains: (saddledata, binedges)
# saddledata is the saddle matrix
saddle_matrix = saddle_data[0]
print(f'Saddle matrix shape: {saddle_matrix.shape}')
```
## Plot Saddle
```python
fig, ax = plt.subplots(figsize=(6, 6))
# Get saddle matrix (aggregate over chromosomes)
saddle_agg = np.nanmean(saddle_data[0], axis=0)
im = ax.imshow(saddle_agg, cmap='coolwarm', vmin=-1, vmax=1)
ax.set_xlabel('E1 (compartment)')
ax.set_ylabel('E1 (compartment)')
ax.set_title('Saddle plot')
plt.colorbar(im, ax=ax, label='log2(O/E)')
# Mark A and B regions
n = saddle_agg.shape[0]
ax.axhline(n/2, color='k', linewidth=0.5)
ax.axvline(n/2, color='k', linewidth=0.5)
ax.text(n*0.25, n*0.25, 'B-B', ha='center', va='center', fontsize=12)
ax.text(n*0.75, n*0.75, 'A-A', ha='center', va='center', fontsize=12)
ax.text(n*0.25, n*0.75, 'B-A', ha='center', va='center', fontsize=12)
ax.text(n*0.75, n*0.25, 'A-B', ha='center', va='center', fontsize=12)
plt.savefig('saddle_plot.png', dpi=150)
```
## Compartment Strength Score
```python
# Compute compartment strength from saddle
def compartment_strength(saddle_matrix):
n = saddle_matrix.shape[0]
half = n // 2
# AA and BB corners
AA = np.nanmean(saddle_matrix[half:, half:])
BB = np.nanmean(saddle_matrix[:half, :half])
AB = np.nanmean(saddle_matrix[:half, half:])
BA = np.nanmean(saddle_matrix[half:, :half])
# Compartment strength = (AA + BB) / (AB + BA)
strength = (AA + BB) / 2 - (AB + BA) / 2
return strength
strength = compartment_strength(saddle_agg)
print(f'Compartment strength: {strength:.3f}')
```
## Plot Eigenvector Track
```python
fig, ax = plt.subplots(figsize=(15, 3))
# Plot for one chromosome
chr_data = eigenvectors[eigenvectors['chrom'] == 'chr1']
# Color by compartment
colors = ['red' if e > 0 else 'blue' for e in chr_data['E1']]
ax.bar(chr_data['start'] / 1e6, chr_data['E1'], width=0.1, color=colors)
ax.axhline(0, color='k', linewidth=0.5)
ax.set_xlabel('Position (Mb)')
ax.set_ylabel('E1 (compartment)')
ax.set_title('chr1 compartments (red=A, blue=B)')
plt.tight_layout()
plt.savefig('compartment_track.png', dpi=150)
```
## Export Compartment Calls
```python
# Save as BED file
compartment_bed = eigenvectors[['chrom', 'start', 'end', 'E1', 'compartment']].copy()
compartment_bed.to_csv('compartments.bed', sep='\t', index=False, header=False)
# Save as bedGraph
eigenvectors[['chrom', 'start', 'end', 'E1']].to_csv(
'compartment_eigenvector.bedgraph',
sep='\t',
index=False,
header=False
)
```
## Compare Compartments Between Samples
```python
# Load two samples
clr1 = cooler.Cooler('sample1.mcool::resolutions/100000')
clr2 = cooler.Cooler('sample2.mcool::resolutions/100000')
# Compute eigenvectors for both
_, eig1 = cooltools.eigs_cis(clr1, view_df=view_df, n_eigs=1)
_, eig2 = cooltools.eigs_cis(clr2, view_df=view_df, n_eigs=1)
# Merge and compare
merged = eig1.merge(eig2, on=['chrom', 'start', 'end'], suffixes=('_1', '_2'))
# Correlation
from scipy.stats import pearsonr
r, p = pearsonr(merged['E1_1'].dropna(), merged['E1_2'].dropna())
print(f'E1 correlation: r={r:.3f}, p={p:.2e}')
# Compartment switches
merged['switch'] = (merged['E1_1'] > 0) != (merged['E1_2'] > 0)
print(f'Compartment switches: {merged["switch"].sum()} bins')
```
## Correlate with Gene Expression
```python
# Load gene expression data
# Assume: gene_expr with columns ['chrom', 'start', 'end', 'expression']
# Bin genes into compartment bins
compartment_expr = eigenvectors.merge(
gene_expr,
on=['chrom'],
how='left'
)
compartment_expr = compartment_expr[
(compartment_expr['start_y'] >= compartment_expr['start_x']) &
(compartment_expr['start_y'] < compartment_expr['end_x'])
]
# Compare expression in A vs B
a_expr = compartment_expr[compartment_expr['compartment'] == 'A']['expression']
b_expr = compartment_expr[compartment_expr['compartment'] == 'B']['expression']
print(f'A compartment expression: {a_expr.mean():.2f}')
print(f'B compartment expression: {b_expr.mean():.2f}')
```
## Related Skills
- matrix-operations - Prepare matrices for compartment analysis
- hic-visualization - Visualize compartments
- chip-seq - Correlate with histone marks
<!-- AUTHOR_SIGNATURE: 9a7f3c2e-MD-BABU-MIA-2026-MSSM-SECURE -->Is this your skill, or is something wrong with this listing? Request removal or report an issue. Author removals are honored within 72 hours.
No comments yet. Be the first to comment!