Agent skill
bio-genome-intervals-interval-arithmetic
Install this agent skill to your Project
npx add-skill https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/bio-genome-intervals-interval-arithmetic
SKILL.md
name: bio-genome-intervals-interval-arithmetic description: Core interval arithmetic operations including intersect, subtract, merge, complement, map, and groupby using bedtools and pybedtools. Use when finding overlapping regions, removing overlaps, combining adjacent intervals, or transferring annotations between interval files. tool_type: mixed primary_tool: bedtools measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:
- read_file
- run_shell_command
Interval Arithmetic
Core set operations on genomic intervals using bedtools (CLI) and pybedtools (Python).
Intersect - Find Overlapping Regions
CLI
# Find overlapping intervals (report A entries that overlap B)
bedtools intersect -a peaks.bed -b genes.bed > overlapping.bed
# Report original A intervals (default behavior)
bedtools intersect -a peaks.bed -b genes.bed > peaks_in_genes.bed
# Report overlapping portion only
bedtools intersect -a peaks.bed -b genes.bed > overlap_regions.bed
# Report both A and B fields
bedtools intersect -a peaks.bed -b genes.bed -wa -wb > with_gene_info.bed
# Write original A entries that overlap B (-u for unique)
bedtools intersect -a peaks.bed -b genes.bed -u > peaks_overlapping_genes.bed
# Report A entries that do NOT overlap B
bedtools intersect -a peaks.bed -b genes.bed -v > peaks_not_in_genes.bed
# Require minimum overlap fraction (50% of A must overlap)
bedtools intersect -a peaks.bed -b genes.bed -f 0.5 > min_50pct.bed
# Reciprocal overlap (both A and B must have 50% overlap)
bedtools intersect -a peaks.bed -b genes.bed -f 0.5 -r > reciprocal_50pct.bed
# Count overlaps
bedtools intersect -a peaks.bed -b genes.bed -c > with_counts.bed
# Multiple B files
bedtools intersect -a peaks.bed -b genes.bed promoters.bed enhancers.bed -names genes promoters enhancers > multi.bed
Python
import pybedtools
a = pybedtools.BedTool('peaks.bed')
b = pybedtools.BedTool('genes.bed')
# Basic intersection
result = a.intersect(b)
# Keep original A entries that overlap
result = a.intersect(b, u=True)
# Report both A and B
result = a.intersect(b, wa=True, wb=True)
# Non-overlapping (inverse)
result = a.intersect(b, v=True)
# Minimum overlap fraction
result = a.intersect(b, f=0.5)
# Reciprocal overlap
result = a.intersect(b, f=0.5, r=True)
# Count overlaps
result = a.intersect(b, c=True)
# Save result
result.saveas('output.bed')
Subtract - Remove Overlapping Regions
CLI
# Remove portions of A that overlap B
bedtools subtract -a regions.bed -b exclude.bed > remaining.bed
# Remove entire A interval if ANY overlap with B
bedtools subtract -a regions.bed -b exclude.bed -A > non_overlapping.bed
# Require minimum overlap before removal
bedtools subtract -a regions.bed -b exclude.bed -f 0.5 > subtract_50pct.bed
Python
import pybedtools
a = pybedtools.BedTool('regions.bed')
b = pybedtools.BedTool('exclude.bed')
# Basic subtraction (remove overlapping portions)
result = a.subtract(b)
# Remove entire interval if any overlap
result = a.subtract(b, A=True)
# Require minimum overlap
result = a.subtract(b, f=0.5)
result.saveas('remaining.bed')
Merge - Combine Overlapping/Adjacent Intervals
CLI
# Merge overlapping intervals (input must be sorted)
bedtools sort -i peaks.bed | bedtools merge > merged.bed
# Merge intervals within N bp of each other
bedtools sort -i peaks.bed | bedtools merge -d 100 > merged_100bp.bed
# Report number of merged intervals
bedtools sort -i peaks.bed | bedtools merge -c 1 -o count > merged_counts.bed
# Aggregate columns (e.g., concatenate names, sum scores)
bedtools sort -i peaks.bed | bedtools merge -c 4,5 -o collapse,sum > merged_agg.bed
# Keep max score
bedtools sort -i peaks.bed | bedtools merge -c 5 -o max > merged_max.bed
# Strand-specific merge
bedtools sort -i peaks.bed | bedtools merge -s > merged_stranded.bed
Python
import pybedtools
bed = pybedtools.BedTool('peaks.bed')
# Basic merge (auto-sorts)
merged = bed.sort().merge()
# Merge within distance
merged = bed.sort().merge(d=100)
# Count merged intervals
merged = bed.sort().merge(c=1, o='count')
# Aggregate columns (collapse names, sum scores)
merged = bed.sort().merge(c='4,5', o='collapse,sum')
# Strand-specific
merged = bed.sort().merge(s=True)
merged.saveas('merged.bed')
Complement - Get Uncovered Regions
CLI
# Get regions NOT covered by intervals (requires genome file)
bedtools complement -i covered.bed -g genome.txt > uncovered.bed
# genome.txt format: chr<TAB>size
# chr1 248956422
# chr2 242193529
# ...
Python
import pybedtools
bed = pybedtools.BedTool('covered.bed')
genome = 'genome.txt' # or dict: {'chr1': (0, 248956422), ...}
# Get complement
uncovered = bed.complement(g=genome)
uncovered.saveas('uncovered.bed')
# Using genome dict
genome_dict = pybedtools.chromsizes('hg38') # Built-in genome sizes
uncovered = bed.complement(genome=genome_dict)
Cluster - Group Overlapping Intervals
CLI
# Assign cluster IDs to overlapping intervals
bedtools sort -i peaks.bed | bedtools cluster > clustered.bed
# Cluster within distance
bedtools sort -i peaks.bed | bedtools cluster -d 100 > clustered_100bp.bed
Python
import pybedtools
bed = pybedtools.BedTool('peaks.bed')
clustered = bed.sort().cluster()
clustered.saveas('clustered.bed')
Multiinter - Find Multi-way Overlaps
CLI
# Find regions covered by multiple files
bedtools multiinter -i sample1.bed sample2.bed sample3.bed > multi_overlap.bed
# With sample names
bedtools multiinter -i sample1.bed sample2.bed sample3.bed \
-names s1 s2 s3 > multi_overlap.bed
# Header output
bedtools multiinter -i sample1.bed sample2.bed sample3.bed -header > multi_overlap.bed
Python
import pybedtools
beds = [pybedtools.BedTool(f) for f in ['s1.bed', 's2.bed', 's3.bed']]
# Note: multiinter requires CLI workaround
result = pybedtools.BedTool().multi_intersect(i=[b.fn for b in beds])
Jaccard - Similarity Metric
CLI
# Calculate Jaccard similarity between two BED files
bedtools jaccard -a sample1.bed -b sample2.bed
# Output: intersection, union, jaccard, n_intersections
Python
import pybedtools
a = pybedtools.BedTool('sample1.bed')
b = pybedtools.BedTool('sample2.bed')
result = a.jaccard(b)
print(f"Jaccard index: {result['jaccard']}")
print(f"Intersection: {result['intersection']} bp")
print(f"Union: {result['union']} bp")
Fisher's Exact Test
CLI
# Statistical test for overlap significance
bedtools fisher -a peaks.bed -b genes.bed -g genome.txt
Python
import pybedtools
a = pybedtools.BedTool('peaks.bed')
b = pybedtools.BedTool('genes.bed')
result = a.fisher(b, genome='genome.txt')
print(result) # Contains p-values and odds ratio
Shuffle - Random Permutation
CLI
# Randomly shuffle intervals (for null hypothesis testing)
bedtools shuffle -i peaks.bed -g genome.txt > shuffled.bed
# Exclude certain regions
bedtools shuffle -i peaks.bed -g genome.txt -excl blacklist.bed > shuffled.bed
# Maintain chromosome distribution
bedtools shuffle -i peaks.bed -g genome.txt -chrom > shuffled.bed
Python
import pybedtools
bed = pybedtools.BedTool('peaks.bed')
shuffled = bed.shuffle(g='genome.txt')
shuffled.saveas('shuffled.bed')
Map - Transfer Values Between Files
Map overlapping B values onto A intervals with aggregation.
CLI
# Map mean scores from B to A
bedtools map -a genes.bed -b scores.bedGraph -c 4 -o mean > genes_with_scores.bed
# Multiple operations at once
bedtools map -a regions.bed -b data.bed -c 5,5,5 -o mean,min,max > multi_stats.bed
# Count overlapping features
bedtools map -a genes.bed -b peaks.bed -c 1 -o count > genes_with_peak_counts.bed
# Collapse names of overlapping features
bedtools map -a genes.bed -b peaks.bed -c 4 -o collapse > genes_with_peak_names.bed
# Distinct values only
bedtools map -a genes.bed -b annotations.bed -c 4 -o distinct > unique_annotations.bed
Python
import pybedtools
a = pybedtools.BedTool('genes.bed')
b = pybedtools.BedTool('scores.bedGraph')
# Map mean scores
result = a.map(b, c=4, o='mean')
# Multiple operations
result = a.map(b, c='5,5,5', o='mean,min,max')
result.saveas('mapped.bed')
Map Operations
| Operation | Description |
|---|---|
| sum | Sum of values |
| count | Number of overlapping features |
| count_distinct | Number of distinct values |
| min, max | Minimum/maximum value |
| mean, median | Average values |
| collapse | Comma-separated list |
| distinct | Unique values only |
| first, last | First/last overlapping value |
Groupby - Aggregate by Columns
Group intervals and compute summary statistics.
CLI
# Sum scores by gene (column 4)
bedtools groupby -i sorted.bed -g 4 -c 5 -o sum > gene_totals.bed
# Group by chromosome and compute stats
bedtools groupby -i sorted.bed -g 1 -c 2,3 -o min,max > chr_ranges.bed
# Multiple grouping columns
bedtools groupby -i sorted.bed -g 1,4 -c 5 -o mean > by_chr_gene.bed
# Collapse names within groups
bedtools groupby -i sorted.bed -g 1,2,3 -c 4 -o collapse > merged_names.bed
# Count features per group
bedtools groupby -i sorted.bed -g 1 -c 1 -o count > features_per_chr.bed
# Use column ranges
bedtools groupby -i sorted.bed -g 1-3 -c 5 -o sum > grouped.bed
Python
import pybedtools
bed = pybedtools.BedTool('sorted.bed')
# Group by column 4, sum column 5
result = bed.groupby(g=4, c=5, o='sum')
# Multiple operations
result = bed.groupby(g=[1, 4], c=[5, 5], o=['mean', 'count'])
result.saveas('grouped.bed')
Note: Input must be sorted by grouping columns.
Common Patterns
Find Peaks in Promoters
import pybedtools
peaks = pybedtools.BedTool('peaks.bed')
promoters = pybedtools.BedTool('promoters.bed')
# Peaks overlapping promoters
peaks_in_promoters = peaks.intersect(promoters, u=True)
print(f'{peaks_in_promoters.count()} peaks in promoters')
Find Unique Regions in Sample
import pybedtools
sample_a = pybedtools.BedTool('sample_a.bed')
sample_b = pybedtools.BedTool('sample_b.bed')
# Regions unique to sample A
unique_a = sample_a.intersect(sample_b, v=True)
unique_a.saveas('unique_to_a.bed')
Merge Replicates
# Concatenate and merge peaks from replicates
cat rep1.bed rep2.bed rep3.bed | bedtools sort | bedtools merge -d 100 > consensus.bed
Key Parameters
| Operation | Key Flags | Description |
|---|---|---|
| intersect -u | Unique | Report A once if overlap |
| intersect -v | Inverse | A that don't overlap B |
| intersect -f | Fraction | Minimum overlap fraction |
| intersect -r | Reciprocal | Both must meet -f threshold |
| intersect -c | Count | Count overlapping B features |
| subtract -A | All | Remove entire A if any overlap |
| merge -d | Distance | Merge within N bp |
| merge -c -o | Columns/Ops | Aggregate columns |
Related Skills
- bed-file-basics - BED format and creation
- proximity-operations - closest, window, flank, slop
- coverage-analysis - coverage calculations
- chip-seq/peak-calling - peak file operations
Recommended Agent Skills
Expand your agent's capabilities with these related and highly-rated skills.
vcf-annotator
Annotate VCF variants with VEP, ClinVar, gnomAD frequencies, and ancestry-aware context. Generates prioritised variant reports.
chemist-analyst
Analyzes events through chemistry lens using molecular structure, reaction mechanisms, thermodynamics, kinetics, and analytical techniques (spectroscopy, chromatography, mass spectrometry). Provides insights on chemical processes, material properties, reaction pathways, synthesis, and analytical methods. Use when: Chemical reactions, material analysis, synthesis planning, process optimization, environmental chemistry. Evaluates: Molecular structure, reaction mechanisms, yield, selectivity, safety, environmental impact.
bio-alignment-io
Read, 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.
sleep-analyzer
分析睡眠数据、识别睡眠模式、评估睡眠质量,并提供个性化睡眠改善建议。支持与其他健康数据的关联分析。
metabolomics-workbench-database
Access NIH Metabolomics Workbench via REST API (4,200+ studies). Query metabolites, RefMet nomenclature, MS/NMR data, m/z searches, study metadata, for metabolomics and biomarker discovery.
bio-hi-c-analysis-matrix-operations
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.
Didn't find tool you were looking for?