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Alignment Sorting - Usage Guide

Overview

Sort BAM files by coordinate or read name for downstream analysis tools that require specific sort orders.

Prerequisites

# samtools
conda install -c bioconda samtools

# pysam
pip install pysam

Quick Start

Tell your AI agent what you want to do: - "Sort my BAM file by coordinate" - "Sort reads by name for duplicate marking" - "Check the current sort order of my BAM file" - "Sort directly from aligner output in a pipeline"

Example Prompts

Coordinate Sorting

"Sort my BAM file by genomic position"

"Sort the output from BWA alignment"

"Verify my BAM is coordinate-sorted"

Name Sorting

"Sort my BAM file by read name"

"Prepare BAM for the fixmate step"

"Sort for extracting paired FASTQ files"

Pipeline Operations

"Align with BWA and sort in one command"

"Run the complete duplicate marking workflow"

"Re-sort an incorrectly sorted BAM file"

Performance Optimization

"Sort with 8 threads and 4GB memory per thread"

"Use a fast SSD for temporary files during sorting"

What the Agent Will Do

  1. Check the current sort order of the input BAM
  2. Select appropriate sort method (coordinate or name)
  3. Configure memory and thread settings for optimal performance
  4. Execute the sort operation
  5. Verify the output file was created successfully
  6. Index the sorted file if coordinate-sorted

Sort Order Requirements

Sort Order Required For
Coordinate Indexing, IGV, variant calling, mpileup
Name fixmate, markdup (first pass), paired FASTQ extraction

Common Commands

Coordinate Sort

samtools sort -o sorted.bam unsorted.bam

# From aligner pipeline
bwa mem ref.fa reads.fq | samtools sort -o aligned.bam

Name Sort

samtools sort -n -o namesorted.bam input.bam

Verify Sort Order

samtools view -H sorted.bam | grep "^@HD"
# @HD VN:1.6 SO:coordinate

Performance Options

samtools sort -@ 8 -o sorted.bam input.bam        # 8 threads
samtools sort -@ 4 -m 4G -o sorted.bam input.bam  # 4GB per thread
samtools sort -T /scratch/tmp -o sorted.bam input.bam  # Fast temp disk
samtools sort -l 1 -o sorted.bam input.bam        # Fast compression

Duplicate Marking Workflow

samtools sort -n -@ 4 input.bam | \
    samtools fixmate -m -@ 4 - - | \
    samtools sort -@ 4 - | \
    samtools markdup -@ 4 - final.bam
samtools index final.bam

Collate vs Sort

# Collate: fast grouping without full sort
samtools collate -u -O input.bam /tmp/prefix | \
    samtools fastq -1 R1.fq -2 R2.fq -0 /dev/null -s /dev/null -

# Full name sort when strict ordering is needed
samtools sort -n -o namesorted.bam input.bam

Python with pysam

Basic Sort

import pysam

pysam.sort('-o', 'sorted.bam', 'input.bam')
pysam.sort('-n', '-o', 'namesorted.bam', 'input.bam')
pysam.sort('-@', '4', '-m', '2G', '-o', 'sorted.bam', 'input.bam')

Check Sort Order

import pysam

def get_sort_order(bam_path):
    with pysam.AlignmentFile(bam_path, 'rb') as bam:
        hd = bam.header.get('HD', {})
        return hd.get('SO', 'unknown')

order = get_sort_order('input.bam')
print(f'Sort order: {order}')

Sort if Needed

import pysam

def ensure_coordinate_sorted(input_bam, output_bam):
    order = get_sort_order(input_bam)
    if order == 'coordinate':
        return input_bam
    pysam.sort('-o', output_bam, input_bam)
    return output_bam

Troubleshooting

Out of Memory

Reduce per-thread memory or number of threads:

samtools sort -@ 4 -m 2G -o sorted.bam input.bam

Disk Full

Temp files filling disk. Use different location:

samtools sort -T /other/disk/tmp -o sorted.bam input.bam

Slow Sorting

Corrupted Output

If sort is interrupted, output may be truncated. Re-run from original input.

Tips