bio-hi-c-analysis-matrix-operations

$npx mdskill add GPTomics/bioSkills/bio-hi-c-analysis-matrix-operations

Balance and normalize Hi-C matrices using cooler and cooltools.

  • Enables iterative correction and expected value computation for contact matrices.
  • Depends on cooler and cooltools libraries with specific version requirements.
  • Executes balancing logic through Python API calls to cooler.balance_cooler.
  • Stores corrected weights directly within the input matrix file structure.

SKILL.md

.github/skills/bio-hi-c-analysis-matrix-operationsView on GitHub ↗
---
name: bio-hi-c-analysis-matrix-operations
description: Balance, normalize, and transform Hi-C contact matrices using cooler and cooltools. Apply iterative correction (ICE), compute expected values, and generate observed/expected matrices. Use when normalizing or transforming Hi-C matrices.
tool_type: python
primary_tool: cooltools
---

## Version Compatibility

Reference examples tested with: cooler 0.9+, cooltools 0.6+, numpy 1.26+, pandas 2.2+, scipy 1.12+

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 Matrix Operations

**"Normalize my Hi-C contact matrix"** → Apply iterative correction (ICE/KR balancing), compute distance-decay expected values, and generate observed/expected ratio matrices.
- Python: `cooler.balance_cooler(clr)`, `cooltools.expected_cis(clr)`

Balance, normalize, and transform contact matrices.

## Required Imports

```python
import cooler
import cooltools
import numpy as np
import pandas as pd
```

## Matrix Balancing (ICE)

```python
# Balance a cooler file (iterative correction)
cooler.balance_cooler('matrix.cool', store=True, cis_only=True)

# The balanced weights are stored in the 'weight' column
clr = cooler.Cooler('matrix.cool')
weights = clr.bins()['weight'][:]
print(f'Balanced weights range: {weights.min():.4f} - {weights.max():.4f}')
```

## Balance with CLI

```bash
# Balance using cooler CLI
cooler balance matrix.cool --cis-only --force

# Check balance status
cooler info matrix.cool | grep "weight"
```

## Access Balanced vs Raw Matrix

```python
clr = cooler.Cooler('matrix.cool')

# Balanced (normalized) matrix
balanced = clr.matrix(balance=True).fetch('chr1')

# Raw (count) matrix
raw = clr.matrix(balance=False).fetch('chr1')

print(f'Raw sum: {raw.sum():.0f}')
print(f'Balanced sum: {np.nansum(balanced):.4f}')
```

## Compute Expected Values

```python
import cooltools

clr = cooler.Cooler('matrix.cool')

# Compute expected (average by distance)
expected = cooltools.expected_cis(clr, ignore_diags=2)
print(expected.head())
# Columns: region1, region2, dist, n_valid, count.sum, balanced.sum, balanced.avg
```

## Observed/Expected Matrix

**Goal:** Remove the distance-dependent decay from a contact matrix so that enriched interactions (loops, compartments) stand out above the background.

**Approach:** Compute the average contact frequency at each genomic distance (expected), then divide each observed pixel by its distance-matched expected value to produce an O/E ratio matrix.

```python
import cooltools

clr = cooler.Cooler('matrix.cool')

# Compute expected
expected = cooltools.expected_cis(clr, ignore_diags=2)

# Get O/E matrix for a region
def get_oe_matrix(clr, region, expected_df):
    matrix = clr.matrix(balance=True).fetch(region)
    n = matrix.shape[0]

    # Get expected values for this chromosome
    chrom = region.split(':')[0]
    exp_chr = expected_df[expected_df['region1'] == chrom]
    exp_values = exp_chr.set_index('dist')['balanced.avg']

    # Create expected matrix
    expected_matrix = np.zeros_like(matrix)
    for i in range(n):
        for j in range(n):
            dist = abs(i - j)
            if dist in exp_values.index:
                expected_matrix[i, j] = exp_values[dist]

    # Compute O/E
    oe = matrix / expected_matrix
    oe[expected_matrix == 0] = np.nan

    return oe

oe_matrix = get_oe_matrix(clr, 'chr1', expected)
```

## Using cooltools for O/E

```python
import cooltools

clr = cooler.Cooler('matrix.cool')

# Compute expected
expected = cooltools.expected_cis(clr, ignore_diags=2)

# Get O/E normalized matrix
# cooltools provides this through the snipping module
from cooltools.lib import snip

# For a specific region pair
region1 = ('chr1', 50000000, 60000000)
region2 = ('chr1', 50000000, 60000000)

# Snippet
snippet = snip.snip_pileup(
    clr.matrix(balance=True),
    region1,
    region2,
    exp_func=None,  # Add expected function for O/E
)
```

## Log Transform

```python
# Log2 transform of O/E matrix
log_oe = np.log2(oe_matrix)
log_oe[np.isinf(log_oe)] = np.nan

print(f'Log2(O/E) range: {np.nanmin(log_oe):.2f} to {np.nanmax(log_oe):.2f}')
```

## Distance Decay Normalization

```python
def distance_normalize(matrix, decay_func=None):
    '''Normalize by expected distance decay'''
    n = matrix.shape[0]
    normalized = np.zeros_like(matrix)

    for diag in range(n):
        diag_values = np.diag(matrix, diag)
        expected = np.nanmean(diag_values) if decay_func is None else decay_func(diag)
        if expected > 0:
            for i in range(n - diag):
                normalized[i, i + diag] = matrix[i, i + diag] / expected
                normalized[i + diag, i] = matrix[i + diag, i] / expected

    return normalized
```

## Aggregate Multiple Replicates

```python
# Sum matrices from multiple replicates
files = ['rep1.cool', 'rep2.cool', 'rep3.cool']
matrices = []

for f in files:
    clr = cooler.Cooler(f)
    m = clr.matrix(balance=False).fetch('chr1')
    matrices.append(m)

# Sum raw matrices
summed = np.sum(matrices, axis=0)

# Then balance the summed result
```

## Smooth Matrix

```python
from scipy.ndimage import uniform_filter

# Apply smoothing
smoothed = uniform_filter(matrix, size=3, mode='constant')

# Gaussian smoothing
from scipy.ndimage import gaussian_filter
smoothed_gauss = gaussian_filter(matrix, sigma=1)
```

## Downsample/Coarsen Matrix

```python
def coarsen_matrix(matrix, factor):
    '''Coarsen matrix by summing bins'''
    n = matrix.shape[0]
    new_n = n // factor
    coarse = np.zeros((new_n, new_n))

    for i in range(new_n):
        for j in range(new_n):
            coarse[i, j] = np.nansum(matrix[
                i*factor:(i+1)*factor,
                j*factor:(j+1)*factor
            ])

    return coarse

coarse_matrix = coarsen_matrix(matrix, factor=10)
```

## Correlation Matrix

```python
# Compute correlation matrix (for compartment analysis)
from scipy.stats import pearsonr

def correlation_matrix(matrix):
    '''Compute Pearson correlation between rows'''
    n = matrix.shape[0]
    corr = np.zeros((n, n))

    # Remove rows with all NaN
    valid_rows = ~np.all(np.isnan(matrix), axis=1)
    valid_matrix = matrix[valid_rows][:, valid_rows]

    for i in range(valid_matrix.shape[0]):
        for j in range(valid_matrix.shape[0]):
            mask = ~(np.isnan(valid_matrix[i]) | np.isnan(valid_matrix[j]))
            if mask.sum() > 2:
                corr[i, j], _ = pearsonr(valid_matrix[i, mask], valid_matrix[j, mask])

    return corr

corr = correlation_matrix(oe_matrix)
```

## Save Modified Matrix

```python
# Save matrix as numpy array
np.save('processed_matrix.npy', oe_matrix)

# Create new cooler with modified values
# (More complex, usually work with existing files)
```

## Related Skills

- hic-data-io - Load and access cooler files
- compartment-analysis - Use O/E matrices for compartments
- hic-visualization - Visualize processed matrices

More from GPTomics/bioSkills

SkillDescription
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.