Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
The English summary is being prepared. Showing the original 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.
The English summary is being prepared. Showing the original description.
Run score Not tested
See how to installReview the instructions the agent will receive before you install.
Reference examples tested with: cooler 0.9+, cooltools 0.6+, matplotlib 3.8+, numpy 1.26+, pandas 2.2+, scipy 1.12+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signaturesIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Identify A/B compartments from my Hi-C data" → Decompose the contact matrix via eigenvector analysis to classify chromatin into active (A) and inactive (B) compartments.
cooltools.eigs_cis(clr, gc_cov) for eigenvector decompositionDetect A/B compartments from Hi-C contact matrices.
import cooler
import cooltools
import cooltools.lib.plotting
import numpy as np
import pandas as pd
import matplotlib.pyplot as plt
import bioframe
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())
# 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,
)
# 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())
# 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}')
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)
Goal: Quantify the degree of compartmentalization by measuring the enrichment of A-A and B-B contacts relative to A-B contacts.
Approach: Partition the saddle matrix into four quadrants (AA, BB, AB, BA) and compute the difference between same-compartment and cross-compartment average contact enrichment.
# 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}')
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)
# 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
)
Goal: Identify genomic regions that switch between A and B compartments across two experimental conditions.
Approach: Compute eigenvectors for both samples, correlate E1 values genome-wide, and flag bins where the sign of E1 flips between conditions.
# 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')
# 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}')
No reviews yet. Tell others what you thought.
No login needed. Share how it worked for you, ask a question, or note where it did not run.
No comments yet. Be the first to write one.
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
The English summary is being prepared. Showing the original description.
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
The English summary is being prepared. Showing the original description.
AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
The English summary is being prepared. Showing the original description.
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
The English summary is being prepared. Showing the original description.
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
The English summary is being prepared. Showing the original description.
End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
The English summary is being prepared. Showing the original description.