bio-bam

name	bio-bam
description	This skill should be used when the user asks to analyze BAM/SAM/CRAM alignment files from WGS/WES sequencing. Triggers include requests to extract reads from specific regions, identify insertions and deletions, calculate coverage statistics, or export read data as JSON for downstream analysis.
user_invocable	true

BAM Toolkit

Toolkit for BAM/SAM/CRAM alignment file analysis: extract reads, identify indels, and calculate coverage. Designed for WGS/WES sequencing result inspection and quality control.

Quick Start

Install

uv pip install pysam typer

Basic Usage

# 1. 特定領域のリードを抽出
python scripts/extract_reads.py --bam alignment.bam --region chr1:1000-2000 --output reads.json --format json

# 2. Indel を抽出
python scripts/extract_indels.py --bam alignment.bam --region chr1:1000-2000 --output indels.json

# 3. カバレッジ統計を計算
python scripts/calculate_coverage.py --bam alignment.bam --region chr1:1000-2000 --output coverage.json

Scripts

extract_reads.py - Read Extraction

Extract reads from BAM/SAM/CRAM files for specific genomic regions and export as BAM or JSON format.

Required Arguments

• --bam PATH - Input BAM/SAM/CRAM file path
• --region TEXT - Genomic region (e.g., chr1:1000-2000)

Optional Arguments

Output:

• --output PATH - Output file path (BAM or JSON based on extension)
• --format TEXT - Output format: bam or json (default: bam)

Filters:

• --min-mapq INT - Minimum mapping quality (default: 0)
• --proper-pairs - Only properly paired reads
• --no-duplicates - Exclude duplicate reads

Output Format (JSON)

{
  "region": "chr1:1000-2000",
  "total_reads": 150,
  "filtered_from": 200,
  "filters": {
    "min_mapq": 30,
    "proper_pairs_only": true,
    "no_duplicates": true
  },
  "reads": [
    {
      "query_name": "read1",
      "reference_start": 1050,
      "reference_end": 1150,
      "sequence": "ATCG...",
      "quality": "IIII...",
      "mapping_quality": 60
       
       
       
       
       
       
       
       
       
    
  

Output Format (BAM)

When --format bam is specified, outputs a filtered BAM file containing only reads that pass the specified filters.

Usage Examples

# Extract reads as JSON
python scripts/extract_reads.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --output reads.json \
  --format json

# Extract reads as BAM
python scripts/extract_reads.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --output reads.bam

# Extract high-quality properly-paired reads
python scripts/extract_reads.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --proper-pairs \
  --no-duplicates \
  --output filtered.bam

extract_indels.py - Insertion/Deletion Extraction

Extract insertions and deletions from reads in specified genomic regions by parsing CIGAR strings.

Required Arguments

• --bam PATH - Input BAM/SAM/CRAM file path
• --region TEXT - Genomic region (e.g., chr1:1000-2000)

Optional Arguments

Output:

• --output PATH - JSON output file path (default: stdout)

Filters:

• --min-mapq INT - Minimum mapping quality (default: 20)
• --min-indel-size INT - Minimum indel size in bp (default: 1)

Output Format (JSON)

{
  "region": "chr1:1000-2000",
  "filters": {
    "min_mapq": 20,
    "min_indel_size": 1
  },
  "reads": {
    "total": 500,
    "processed": 450
  },
  "summary": {
    "total_insertions": 15,
    "total_deletions": 8,
    "unique_insertions": 5,
    "unique_deletions": 3
  },
  "insertions": [
    {
      "position": 1050,
      "size" 
       
       
       
       
         
    
  
   
    
       
       
       
       
       
        
    
  

Implementation Details

• Parses CIGAR strings to identify I (insertion) and D (deletion) operations
• Extracts sequences for insertions from read sequences
• Groups identical indels by position and sequence/size
• Counts supporting reads for each unique indel
• Filters by mapping quality and minimum indel size

Usage Examples

# Extract all indels
python scripts/extract_indels.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --output indels.json

# Extract large indels only (>= 5bp)
python scripts/extract_indels.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-indel-size 5 \
  --output large_indels.json

# High-quality indels only
python scripts/extract_indels.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --output hq_indels.json

calculate_coverage.py - Coverage Calculation

Calculate coverage statistics for specified genomic regions using pileup operations.

Required Arguments

• --bam PATH - Input BAM/SAM/CRAM file path
• --region TEXT - Genomic region (e.g., chr1:1000-2000)

Optional Arguments

Output:

• --output PATH - JSON output file path (default: stdout)

Options:

• --min-mapq INT - Minimum mapping quality (default: 0)
• --min-baseq INT - Minimum base quality (default: 0)

Output Format (JSON)

{
  "region": "chr1:1000-2000",
  "filters": {
    "min_mapq": 0,
    "min_baseq": 0
  },
  "statistics": {
    "total_bases": 1000,
    "mean_coverage": 45.3,
    "median_coverage": 48,
    "min_coverage": 0,
    "max_coverage": 120,
    "bases_with_coverage": 995,
    "bases_without_coverage": 5,
    "percent_covered": 99.5
  }
}

Usage Examples

# Calculate coverage statistics
python scripts/calculate_coverage.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --output coverage.json

# High-quality bases only
python scripts/calculate_coverage.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --min-baseq 20 \
  --output hq_coverage.json

Workflow Examples

Example 1: Comprehensive Read Analysis Workflow

Combine all three scripts for complete BAM analysis:

# Step 1: Calculate coverage statistics
python scripts/calculate_coverage.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --output coverage.json

# Step 2: Extract indels
python scripts/extract_indels.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --output indels.json

# Step 3: Extract reads as JSON for detailed inspection
python scripts/extract_reads.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --format json \
  --output reads.json

Example 2: High-Quality Indel Discovery

Identify large insertions and deletions with high-quality reads:

# Extract large indels (>= 10bp) with high mapping quality
python scripts/extract_indels.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --min-indel-size 10 \
  --output large_indels.json

# Extract supporting reads for manual validation
python scripts/extract_reads.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --output supporting_reads.bam

Example 3: Coverage Quality Control

Assess sequencing coverage quality across target region:

# Calculate coverage statistics with quality filters
python scripts/calculate_coverage.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --min-baseq 20 \
  --output coverage_stats.json

# Extract reads from low-coverage regions for inspection
python scripts/extract_reads.py \
  --bam alignment.bam \
  --region chr1:1500-1600 \
  --format json \
  --output low_coverage_reads.json

Error Handling

Missing BAM Index

$ python scripts/extract_reads.py --bam alignment.bam --region chr1:1000-2000

Error fetching reads: random access requires an index
Make sure the region 'chr1:1000-2000' exists and BAM file is indexed.

Solution: Create BAM index with samtools:

samtools index alignment.bam

Invalid Region Format

$ python scripts/extract_reads.py --bam alignment.bam --region 1000-2000

Error: Invalid region format: 1000-2000. Expected format: chr1:1000-2000

Solution: Use correct region format chr:start-end:

python scripts/extract_reads.py --bam alignment.bam --region chr1:1000-2000

Best Practices

1. Always Index BAM Files

Create BAM index before using any scripts to enable efficient random access:

# ✅ Good: Index BAM file first
samtools index alignment.bam

# Then use bam-toolkit scripts
python scripts/extract_reads.py --bam alignment.bam --region chr1:1000-2000

2. Apply Quality Filters for Reliable Results

Use mapping quality and base quality filters to ensure reliable analysis:

# ✅ Good: Apply quality filters
python scripts/extract_indels.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30

# ✅ Good: Use proper pairs for structural variant analysis
python scripts/extract_reads.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --proper-pairs \
  --no-duplicates

3. Extract Reads as BAM for Further Processing

Use BAM output when planning to use extracted reads with other tools:

# ✅ Good: Extract as BAM for use with samtools/IGV
python scripts/extract_reads.py \
  --bam alignment.bam \
  --region chr1:1000-2000 \
  --min-mapq 30 \
  --output filtered.bam

# Then index and use with other tools
samtools index filtered.bam
samtools view filtered.bam

When to Use bam-toolkit vs samtools

Task	bam-toolkit	samtools
Read extraction as JSON	✅ extract_reads.py	-
Indel extraction with grouping	✅ extract_indels.py	-
Coverage statistics as JSON	✅ calculate_coverage.py	✅ samtools depth
BAM-to-BAM filtering	✅ extract_reads.py	✅ samtools view
Read alignment statistics	-	✅ samtools flagstat
BAM indexing	-	✅ samtools index

Recommended Workflow:

1. Index BAM files with samtools
2. Use bam-toolkit scripts for structured JSON output
3. Use samtools for standard BAM operations (sorting, indexing, format conversion)

Related Skills

• vcf-toolkit - VCF/BCF variant file operations
• sequence-io - FASTA/FASTQ sequence file operations
• blast-search - BLAST homology search
• blat-api-searching - BLAT genome mapping

Troubleshooting

BAM File Not Readable

Ensure BAM file is properly formatted and readable:

# Check BAM file integrity
samtools quickcheck alignment.bam

# View BAM header
samtools view -H alignment.bam

Chromosome Name Mismatch

Chromosome names must match between BAM file and region specification:

# Check chromosome names in BAM
samtools idxstats alignment.bam | cut -f1

# Use correct chromosome name
# If BAM uses "1" instead of "chr1":
python scripts/extract_reads.py --bam alignment.bam --region 1:1000-2000

Empty Output

If output is empty, check:

1. Region contains aligned reads: samtools view alignment.bam chr1:1000-2000 | head
2. Filters are not too restrictive (try reducing --min-mapq)
3. Chromosome name matches BAM file