Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Process Hi-C read pairs using pairtools. Parse alignments, filter duplicates, classify pairs, and generate contact statistics from Hi-C sequencing data. Use when processing raw Hi-C read pairs.
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Run score Not tested
See how to installReview the instructions the agent will receive before you install.
Reference examples tested with: cooler 0.9+, pairtools 1.1+, pandas 2.2+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signatures<tool> --version then <tool> --help to confirm flagsIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Process my Hi-C read pairs" → Parse aligned Hi-C reads into contact pairs, filter duplicates, classify pair types (cis/trans), and generate contact statistics.
pairtools parse → pairtools sort → pairtools dedup → pairtools statsProcess Hi-C read pairs with pairtools.
BAM (aligned reads)
|
v
pairtools parse (extract pairs)
|
v
pairtools sort
|
v
pairtools dedup (remove duplicates)
|
v
pairtools select (filter by type)
|
v
Valid pairs for matrix generation
# Parse BAM to pairs format
pairtools parse \
--chroms-path chromsizes.txt \
--min-mapq 30 \
--walks-policy 5unique \
--output parsed.pairs.gz \
aligned.bam
# With restriction enzyme cut sites
pairtools parse \
--chroms-path chromsizes.txt \
--min-mapq 30 \
--walks-policy 5unique \
--add-columns mapq \
aligned.bam | \
pairtools restrict -f enzyme_sites.bed | \
gzip > parsed.restricted.pairs.gz
# Sort pairs by position
pairtools sort \
--nproc 8 \
--output sorted.pairs.gz \
parsed.pairs.gz
# Mark and remove PCR duplicates
pairtools dedup \
--max-mismatch 1 \
--mark-dups \
--output deduped.pairs.gz \
--output-stats dedup_stats.txt \
sorted.pairs.gz
# Without outputting dups
pairtools dedup \
--max-mismatch 1 \
--output deduped.pairs.gz \
sorted.pairs.gz
# View header
pairtools header deduped.pairs.gz
# View first few pairs
zcat deduped.pairs.gz | head -100
# Pairs format: readID chrom1 pos1 chrom2 pos2 strand1 strand2 pair_type
# Select only valid pairs (UU = unique-unique mapping)
pairtools select '(pair_type == "UU")' \
--output valid_pairs.pairs.gz \
deduped.pairs.gz
# Multiple types
pairtools select '(pair_type == "UU") or (pair_type == "RU") or (pair_type == "UR")' \
--output all_valid.pairs.gz \
deduped.pairs.gz
# Remove self-ligations (very short range)
pairtools select '(chrom1 != chrom2) or (abs(pos1 - pos2) > 1000)' \
--output filtered.pairs.gz \
deduped.pairs.gz
# If MAPQ column was added during parsing
pairtools select '(mapq1 >= 30) and (mapq2 >= 30)' \
--output hq_pairs.pairs.gz \
deduped.pairs.gz
# Get pair statistics
pairtools stats \
--output stats.txt \
deduped.pairs.gz
# View stats
cat stats.txt
# Split into different files by pair type
pairtools split \
--output-pairs valid.pairs.gz \
--output-sam unmapped.sam \
parsed.pairs.gz
# Merge multiple pairs files
pairtools merge \
--output merged.pairs.gz \
sample1.pairs.gz sample2.pairs.gz sample3.pairs.gz
# Then dedup the merged file
pairtools sort merged.pairs.gz | pairtools dedup > merged_dedup.pairs.gz
# Create restriction site fragments
# First generate sites with cooler
cooler digest hg38.fa HindIII > hindiii_sites.bed
# Then use pairtools restrict
pairtools restrict -f hindiii_sites.bed \
--output restricted.pairs.gz \
parsed.pairs.gz
# Pairs to 2D positions (for visualization)
zcat valid.pairs.gz | awk 'BEGIN{OFS="\t"} !/^#/ {print $2,$3,$4,$5}' > contacts_2d.txt
# Pairs to BEDPE
zcat valid.pairs.gz | awk 'BEGIN{OFS="\t"} !/^#/ {print $2,$3,$3+1,$4,$5,$5+1,$1,1,$6,$7}' > contacts.bedpe
# Aggregate pairs into cooler matrix
cooler cload pairs \
-c1 2 -p1 3 -c2 4 -p2 5 \
chromsizes.txt:10000 \
valid.pairs.gz \
matrix.cool
import pandas as pd
# Read pairs file (skip header)
with open('valid.pairs.gz', 'rt') as f:
header_lines = 0
for line in f:
if line.startswith('#'):
header_lines += 1
else:
break
pairs = pd.read_csv(
'valid.pairs.gz',
sep='\t',
skiprows=header_lines,
names=['readID', 'chrom1', 'pos1', 'chrom2', 'pos2', 'strand1', 'strand2', 'pair_type']
)
print(f'Total pairs: {len(pairs):,}')
print(f'\nPair types:')
print(pairs['pair_type'].value_counts())
Goal: Process raw Hi-C alignments into a balanced contact matrix ready for downstream analysis (TADs, loops, compartments).
Approach: Chain pairtools operations (parse, restrict, sort, dedup, select) into a single pipeline, then aggregate valid pairs into a cooler matrix file.
#!/bin/bash
SAMPLE=$1
CHROMSIZES=chromsizes.txt
ENZYME_SITES=hindiii_sites.bed
# Parse
pairtools parse \
--chroms-path $CHROMSIZES \
--min-mapq 30 \
--walks-policy 5unique \
${SAMPLE}.bam | \
pairtools restrict -f $ENZYME_SITES | \
pairtools sort --nproc 8 | \
pairtools dedup \
--max-mismatch 1 \
--output-stats ${SAMPLE}.dedup_stats.txt | \
pairtools select '(pair_type == "UU")' \
--output ${SAMPLE}.valid.pairs.gz
# Generate matrix
cooler cload pairs \
-c1 2 -p1 3 -c2 4 -p2 5 \
${CHROMSIZES}:10000 \
${SAMPLE}.valid.pairs.gz \
${SAMPLE}.cool
# Stats
pairtools stats ${SAMPLE}.valid.pairs.gz > ${SAMPLE}.stats.txt
echo "Done processing $SAMPLE"
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The English summary is being prepared. Showing the original description.
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The English summary is being prepared. Showing the original description.
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The English summary is being prepared. Showing the original description.