| name | bio-hi-c-analysis-hic-visualization |
| description | Visualize Hi-C contact matrices, TADs, loops, and genomic features using matplotlib, cooltools, and HiCExplorer. Create triangle plots, virtual 4C, and multi-track figures. Use when visualizing contact matrices or genomic features. |
| tool_type | python |
| primary_tool | cooltools |
Version Compatibility
Reference examples tested with: cooler 0.9+, cooltools 0.6+, matplotlib 3.8+, numpy 1.26+, pandas 2.2+
Before using code patterns, verify installed versions match. If versions differ:
- Python:
pip show <package> then help(module.function) to check signatures
- 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.
Hi-C Visualization
"Plot my Hi-C contact matrix" → Create triangle heatmaps, virtual 4C profiles, and multi-track figures combining contact maps with genomic annotations.
- Python:
matplotlib.pyplot.imshow() on cooler matrices, cooltools for aggregate plots
- CLI:
hicPlotMatrix (HiCExplorer)
Visualize Hi-C contact matrices and genomic features.
Required Imports
import cooler
import cooltools
import cooltools.lib.plotting
import numpy as np
import matplotlib.pyplot as plt
from matplotlib.colors import LogNorm
import bioframe
Basic Contact Matrix Plot
clr = cooler.Cooler('matrix.mcool::resolutions/10000')
matrix = clr.matrix(balance=True).fetch('chr1:50000000-60000000')
fig, ax = plt.subplots(figsize=(8, 8))
im = ax.imshow(matrix, cmap='Reds', norm=LogNorm(vmin=0.001, vmax=0.1))
plt.colorbar(im, ax=ax, label='Balanced contacts')
ax.set_title('chr1:50-60Mb')
plt.savefig('contact_matrix.png', dpi=150)
Triangle (Upper Triangle) Plot
def plot_triangle(matrix, ax, cmap='Reds', vmin=None, vmax=None):
'''Plot Hi-C matrix as triangle (rotated 45 degrees)'''
n = matrix.shape[0]
rotated = np.zeros((n, 2*n))
for i in range(n):
for j in range(i, n):
y = j - i
x = i + j
rotated[y, x] = matrix[i, j]
im = ax.imshow(rotated[:n//2, :], cmap=cmap, aspect='auto',
norm=LogNorm(vmin=vmin, vmax=vmax) if vmin else None)
ax.set_ylim(n//2, 0)
return im
matrix = clr.matrix(balance=True).fetch('chr1:50000000-60000000')
fig, ax = plt.subplots(figsize=(12, 4))
im = plot_triangle(matrix, ax, vmin=0.001, vmax=0.1)
plt.colorbar(im, ax=ax)
plt.savefig('triangle_plot.png', dpi=150)
Plot with TADs
import pandas as pd
matrix = clr.matrix(balance=True).fetch('chr1:50000000-60000000')
tads = pd.read_csv('tads.bed', sep='\t', names=['chrom', 'start', 'end'])
fig, ax = plt.subplots(figsize=(8, 8))
im = ax.imshow(matrix, cmap='Reds', norm=LogNorm(vmin=0.001, vmax=0.1))
region_start = 50000000
bin_size = clr.binsize
for _, tad in tads[tads['chrom'] == 'chr1'].iterrows():
if region_start <= tad['start'] < 60000000:
pos = (tad['start'] - region_start) / bin_size
ax.axhline(pos, color='blue', linewidth=0.5, alpha=0.5)
ax.axvline(pos, color='blue', linewidth=0.5, alpha=0.5)
plt.colorbar(im, ax=ax)
plt.savefig('matrix_with_tads.png', dpi=150)
Plot with Loops
matrix = clr.matrix(balance=True).fetch('chr1:50000000-60000000')
loops = pd.read_csv('loops.bedpe', sep='\t')
fig, ax = plt.subplots(figsize=(8, 8))
im = ax.imshow(matrix, cmap='Reds', norm=LogNorm(vmin=0.001, vmax=0.1))
region_start = 50000000
bin_size = clr.binsize
for _, loop in loops[loops['chrom1'] == 'chr1'].iterrows():
if (region_start <= loop['start1'] < 60000000 and
region_start <= loop['start2'] < 60000000):
x = (loop['start1'] - region_start) / bin_size
y = (loop['start2'] - region_start) / bin_size
circle = plt.Circle((y, x), 3, fill=False, color='blue', linewidth=1)
ax.add_patch(circle)
plt.colorbar(im, ax=ax)
plt.savefig('matrix_with_loops.png', dpi=150)
Compare Two Matrices
clr1 = cooler.Cooler('sample1.mcool::resolutions/10000')
clr2 = cooler.Cooler('sample2.mcool::resolutions/10000')
region = 'chr1:50000000-60000000'
mat1 = clr1.matrix(balance=True).fetch(region)
mat2 = clr2.matrix(balance=True).fetch(region)
fig, axes = plt.subplots(1, 3, figsize=(15, 5))
im1 = axes[0].imshow(mat1, cmap='Reds', norm=LogNorm(vmin=0.001, vmax=0.1))
axes[0].set_title('Sample 1')
plt.colorbar(im1, ax=axes[0])
im2 = axes[1].imshow(mat2, cmap='Reds', norm=LogNorm(vmin=0.001, vmax=0.1))
axes[1].set_title('Sample 2')
plt.colorbar(im2, ax=axes[1])
log2fc = np.log2(mat2 / mat1)
log2fc[np.isinf(log2fc)] = np.nan
im3 = axes[2].imshow(log2fc, cmap='coolwarm', vmin=-2, vmax=2)
axes[2].set_title('Log2(Sample2/Sample1)')
plt.colorbar(im3, ax=axes[2])
plt.tight_layout()
plt.savefig('comparison.png', dpi=150)
Split View (Upper/Lower Triangle)
mat1 = clr1.matrix(balance=True).fetch(region)
mat2 = clr2.matrix(balance=True).fetch(region)
combined = np.triu(mat1) + np.tril(mat2, k=-1)
fig, ax = plt.subplots(figsize=(8, 8))
im = ax.imshow(combined, cmap='Reds', norm=LogNorm(vmin=0.001, vmax=0.1))
ax.axline((0, 0), slope=1, color='black', linewidth=0.5)
ax.set_title('Sample1 (upper) vs Sample2 (lower)')
plt.colorbar(im, ax=ax)
plt.savefig('split_view.png', dpi=150)
Virtual 4C
Goal: Extract a one-dimensional contact frequency profile from a single viewpoint locus, simulating a 4C experiment from Hi-C data.
Approach: Select the matrix row corresponding to the viewpoint bin, extract balanced contact values across the chromosome, and plot as a filled line graph.
def virtual_4c(clr, viewpoint_chrom, viewpoint_pos, resolution=10000):
'''Extract virtual 4C from Hi-C'''
viewpoint_bin = viewpoint_pos // resolution
matrix = clr.matrix(balance=True).fetch(viewpoint_chrom)
v4c = matrix[viewpoint_bin, :]
bins = clr.bins().fetch(viewpoint_chrom)
coords = bins['start'].values
return coords, v4c
coords, v4c = virtual_4c(clr, 'chr1', 55000000)
fig, ax = plt.subplots(figsize=(12, 3))
ax.fill_between(coords / 1e6, 0, v4c, alpha=0.5)
ax.axvline(55, color='red', linestyle='--', label='Viewpoint')
ax.set_xlabel('Position (Mb)')
ax.set_ylabel('Contact frequency')
ax.set_title('Virtual 4C from chr1:55Mb')
ax.legend()
plt.savefig('virtual_4c.png', dpi=150)
Multi-Track Figure
fig = plt.figure(figsize=(12, 10))
ax1 = fig.add_axes([0.1, 0.5, 0.8, 0.4])
matrix = clr.matrix(balance=True).fetch('chr1:50000000-60000000')
plot_triangle(matrix, ax1, vmin=0.001, vmax=0.1)
ax1.set_ylabel('Hi-C')
ax2 = fig.add_axes([0.1, 0.35, 0.8, 0.1])
insulation = pd.read_csv('insulation.bedgraph', sep='\t',
names=['chrom', 'start', 'end', 'score'])
ins_region = insulation[(insulation['chrom'] == 'chr1') &
(insulation['start'] >= 50000000) &
(insulation['end'] <= 60000000)]
ax2.plot(ins_region['start'] / 1e6, ins_region['score'])
ax2.set_ylabel('Insulation')
ax2.set_xlim(50, 60)
ax3 = fig.add_axes([0.1, 0.2, 0.8, 0.1])
ax3.set_ylabel('Genes')
ax3.set_xlim(50, 60)
ax4 = fig.add_axes([0.1, 0.05, 0.8, 0.1])
ax4.set_xlabel()
ax4.set_ylabel()
ax4.set_xlim(, )
plt.savefig(, dpi=)
Using HiCExplorer Visualization
hicPlotMatrix \
-m matrix.cool \
--region chr1:50000000-60000000 \
--log1p \
--colorMap Reds \
-o hic_plot.png
hicPlotTADs \
--tracks tracks.ini \
--region chr1:50000000-60000000 \
-o tad_plot.png
Cooltools Pileup Plot
import cooltools
pileup = cooltools.pileup(
clr,
features=loops[['chrom1', 'start1', 'end1', 'chrom2', 'start2', 'end2']],
view_df=view_df,
expected=expected,
flank=100000,
)
avg_pileup = np.nanmean(pileup, axis=2)
fig, ax = plt.subplots(figsize=(6, 6))
im = ax.imshow(avg_pileup, cmap='Reds')
ax.set_title('Average pileup at loops')
plt.colorbar(im, ax=ax)
plt.savefig('pileup.png', dpi=150)
Related Skills
- hic-data-io - Load contact matrices
- tad-detection - Generate TADs to visualize
- loop-calling - Generate loops to visualize
- compartment-analysis - Visualize compartments