OpenClaw-Medical-Skills bio-hi-c-analysis-loop-calling
Detect chromatin loops and point interactions from Hi-C data using cooltools, chromosight, and HiCCUPS-like methods. Identify CTCF-mediated loops and enhancer-promoter contacts. Use when detecting chromatin loops from Hi-C data.
git clone https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.claude/skills && cp -r "$T/skills/bio-hi-c-analysis-loop-calling" ~/.claude/skills/freedomintelligence-openclaw-medical-skills-bio-hi-c-analysis-loop-calling && rm -rf "$T"
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.openclaw/skills && cp -r "$T/skills/bio-hi-c-analysis-loop-calling" ~/.openclaw/skills/freedomintelligence-openclaw-medical-skills-bio-hi-c-analysis-loop-calling && rm -rf "$T"
skills/bio-hi-c-analysis-loop-calling/SKILL.mdVersion Compatibility
Reference examples tested with: bedtools 2.31+, cooler 0.9+, cooltools 0.6+, matplotlib 3.8+, numpy 1.26+, pandas 2.2+, pybedtools 0.9+
Before using code patterns, verify installed versions match. If versions differ:
- Python:
thenpip show <package>
to check signatureshelp(module.function) - CLI:
then<tool> --version
to confirm flags<tool> --help
If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
Chromatin Loop Calling
"Call chromatin loops from my Hi-C data" → Detect point enrichments in contact matrices representing CTCF-mediated loops and enhancer-promoter interactions.
- Python:
orcooltools.dots()chromosight detect --pattern=loops
Detect chromatin loops and point interactions from Hi-C data.
Required Imports
import cooler import cooltools import numpy as np import pandas as pd import matplotlib.pyplot as plt import bioframe
Call Loops with cooltools (Dot Calling)
clr = cooler.Cooler('matrix.mcool::resolutions/10000') view_df = bioframe.make_viewframe(clr.chromsizes) # Compute expected values expected = cooltools.expected_cis(clr, view_df=view_df, ignore_diags=2) # Call dots (loops) dots = cooltools.dots( clr, expected=expected, view_df=view_df, max_loci_separation=2000000, # Max loop size (2Mb) max_nans_tolerated=0.5, ) print(f'Found {len(dots)} loops') print(dots.head())
Using chromosight (CLI)
# Call loops with chromosight chromosight detect \ --pattern loops \ --min-dist 20000 \ --max-dist 2000000 \ matrix.cool \ loops_output # Output: loops_output.tsv with loop coordinates and scores
Parse chromosight Output
loops = pd.read_csv('loops_output.tsv', sep='\t') print(f'Found {len(loops)} loops') print(loops.head()) # Columns: chrom1, start1, end1, chrom2, start2, end2, score, etc.
Using HiCExplorer hicDetectLoops
# Call loops with HiCExplorer hicDetectLoops \ -m matrix.cool \ -o loops.bedgraph \ --maxLoopDistance 2000000 \ --windowSize 10 \ --peakWidth 6 \ --pValuePreselection 0.05 \ --pValue 0.05
Loop Statistics
# Calculate loop sizes loops['size'] = abs(loops['end2'] - loops['start1']) print('Loop size statistics:') print(f' Mean: {loops["size"].mean() / 1000:.0f} kb') print(f' Median: {loops["size"].median() / 1000:.0f} kb') print(f' Min: {loops["size"].min() / 1000:.0f} kb') print(f' Max: {loops["size"].max() / 1000:.0f} kb') # Size distribution plt.hist(loops['size'] / 1000, bins=50) plt.xlabel('Loop size (kb)') plt.ylabel('Count') plt.savefig('loop_sizes.png', dpi=150)
Filter Loops by Score
# Keep high-confidence loops score_threshold = loops['score'].quantile(0.75) high_conf_loops = loops[loops['score'] >= score_threshold] print(f'High confidence loops: {len(high_conf_loops)}')
Annotate Loops with Features
import pybedtools # Convert loop anchors to BED anchor1 = loops[['chrom1', 'start1', 'end1']].copy() anchor1.columns = ['chrom', 'start', 'end'] anchor2 = loops[['chrom2', 'start2', 'end2']].copy() anchor2.columns = ['chrom', 'start', 'end'] # Load CTCF peaks ctcf_peaks = pybedtools.BedTool('ctcf_peaks.bed') # Intersect anchors with CTCF anchor1_bed = pybedtools.BedTool.from_dataframe(anchor1) anchor1_ctcf = anchor1_bed.intersect(ctcf_peaks, wa=True, u=True) print(f'Anchors with CTCF: {len(anchor1_ctcf)} / {len(anchor1)}')
Compare Loops Between Conditions
# Load loops from two conditions loops1 = pd.read_csv('condition1_loops.bedpe', sep='\t') loops2 = pd.read_csv('condition2_loops.bedpe', sep='\t') # Find overlapping loops tolerance = 20000 # 20kb def loops_overlap(l1, l2, tol): return (l1['chrom1'] == l2['chrom1'] and l1['chrom2'] == l2['chrom2'] and abs(l1['start1'] - l2['start1']) <= tol and abs(l1['start2'] - l2['start2']) <= tol) shared = [] for _, loop1 in loops1.iterrows(): for _, loop2 in loops2.iterrows(): if loops_overlap(loop1, loop2, tolerance): shared.append(loop1) break print(f'Shared loops: {len(shared)}') print(f'Condition 1 specific: {len(loops1) - len(shared)}') print(f'Condition 2 specific: {len(loops2) - len(set(range(len(loops2))) - set([]))}')
Aggregate Peak Analysis (APA)
Goal: Assess the overall strength and validity of called loops by stacking contact sub-matrices centered on loop anchors and averaging the signal.
Approach: For each loop, extract a fixed-size snippet from the contact matrix centered on the loop anchor pair, then compute the element-wise mean across all snippets to produce an aggregate enrichment map.
# Stack loops and compute average signal from cooltools.lib import snip def compute_apa(clr, loops, window=100000, resolution=10000): '''Compute average peak analysis''' flank = window // resolution stacks = [] for _, loop in loops.iterrows(): try: # Get region around loop snippet = clr.matrix(balance=True).fetch( f"{loop['chrom1']}:{loop['start1']-window}-{loop['end1']+window}", f"{loop['chrom2']}:{loop['start2']-window}-{loop['end2']+window}" ) if snippet.shape[0] == snippet.shape[1]: stacks.append(snippet) except: continue if len(stacks) > 0: apa = np.nanmean(stacks, axis=0) return apa return None apa_matrix = compute_apa(clr, loops.head(100)) if apa_matrix is not None: plt.imshow(np.log2(apa_matrix), cmap='Reds') plt.colorbar(label='log2(contact)') plt.title('Aggregate Peak Analysis') plt.savefig('apa.png', dpi=150)
Using cooltools pileup for APA
import cooltools # Compute pileup (APA) stack = cooltools.pileup( clr, features=loops[['chrom1', 'start1', 'end1', 'chrom2', 'start2', 'end2']], view_df=view_df, expected=expected, flank=100000, ) # Average across all features apa = np.nanmean(stack, axis=2)
Export Loops
# Save as BEDPE loops[['chrom1', 'start1', 'end1', 'chrom2', 'start2', 'end2', 'score']].to_csv( 'loops.bedpe', sep='\t', index=False, header=False ) # Save as Juicer format (for visualization in Juicebox) loops_juicer = loops.copy() loops_juicer['color'] = '0,0,255' # Blue loops_juicer[['chrom1', 'start1', 'end1', 'chrom2', 'start2', 'end2', 'color']].to_csv( 'loops.2dbed', sep='\t', index=False, header=False )
Loops at Promoter-Enhancer Pairs
# Check if loops connect promoters and enhancers promoters = pd.read_csv('promoters.bed', sep='\t', names=['chrom', 'start', 'end', 'gene']) enhancers = pd.read_csv('enhancers.bed', sep='\t', names=['chrom', 'start', 'end']) # For each loop, check if one anchor is promoter, other is enhancer pe_loops = [] for _, loop in loops.iterrows(): # Check anchor 1 anchor1_prom = any((promoters['chrom'] == loop['chrom1']) & (promoters['start'] <= loop['end1']) & (promoters['end'] >= loop['start1'])) anchor1_enh = any((enhancers['chrom'] == loop['chrom1']) & (enhancers['start'] <= loop['end1']) & (enhancers['end'] >= loop['start1'])) # Check anchor 2 anchor2_prom = any((promoters['chrom'] == loop['chrom2']) & (promoters['start'] <= loop['end2']) & (promoters['end'] >= loop['start2'])) anchor2_enh = any((enhancers['chrom'] == loop['chrom2']) & (enhancers['start'] <= loop['end2']) & (enhancers['end'] >= loop['start2'])) if (anchor1_prom and anchor2_enh) or (anchor1_enh and anchor2_prom): pe_loops.append(loop) print(f'Promoter-enhancer loops: {len(pe_loops)}')
Related Skills
- hic-data-io - Load Hi-C matrices
- hic-visualization - Visualize loops
- chip-seq - CTCF ChIP-seq for loop anchor validation