BarcodeSeqKit 0.0.3

BarcodeSeqKit is a library designed for extracting and processing barcoded sequences from next-generation sequencing data.

BarcodeSeqKit

Key Features

• Simple yet powerful: Extract barcodes from BAM or FASTQ files with minimal code
• Support for both file types: Process BAM files (including softclipped regions) and FASTQ files (including paired-end data)
• Flexible barcode options: Use single barcodes or specific 5’/3’ combinations
• Orientation detection: Identify barcodes in both forward and reverse complement orientations
• Fuzzy matching: Configure allowable mismatches for barcode detection
• Specialized functions: Search in softclipped regions of BAM alignments or both reads in paired FASTQ data
• Detailed statistics: Get comprehensive reports on barcode matches and distribution

Installation

You can install BarcodeSeqKit using pip:

pip install barcodeseqkit

Or directly from the GitHub repository:

pip install git+https://github.com/username/BarcodeSeqKit.git

Quick Start

Let’s dive right in with some common use cases!

Command-line Usage

BarcodeSeqKit provides a simple command-line interface that makes it easy to extract barcodes without writing any code.

Extract a Single Barcode

barcodeseqkit --bam tests/test.bam \
              --barcode CTGACTCCTTAAGGGCC \
              --output-prefix single_barcode \
              --output-dir results

This command extracts reads containing the specified barcode (in either forward or reverse complement orientation) and creates: - results/single_barcode_barcode_orientFR.bam: Forward orientation matches - results/single_barcode_barcode_orientRC.bam: Reverse complement matches - results/single_barcode_extraction_stats.json: Detailed statistics in JSON format - results/single_barcode_extraction_stats.tsv: Detailed statistics in TSV format

Extract 5’ and 3’ Barcodes

barcodeseqkit --bam tests/test.bam \
              --barcode5 CTGACTCCTTAAGGGCC \
              --barcode3 TAACTGAGGCCGGC \
              --output-prefix dual_barcode \
              --output-dir results

This creates separate files for each barcode and orientation combination: - results/dual_barcode_barcode5_orientFR.bam - results/dual_barcode_barcode5_orientRC.bam - results/dual_barcode_barcode3_orientFR.bam - results/dual_barcode_barcode3_orientRC.bam

Process Paired FASTQ Files

barcodeseqkit --fastq1 tests/test.1.fastq.gz \
              --fastq2 tests/test.2.fastq.gz \
              --barcode CTGACTCCTTAAGGGCC \
              --output-prefix fastq_extraction \
              --search-both-reads

This processes paired FASTQ files and creates output FASTQ files for each barcode category.

Python API Usage

BarcodeSeqKit’s Python API is designed to be intuitive and straightforward:

from BarcodeSeqKit.core import BarcodeConfig, BarcodeLocationType, BarcodeExtractorConfig
from BarcodeSeqKit.bam_processing import process_bam_file

# Define barcodes
barcodes = [
    BarcodeConfig(
        sequence="TAACTGAGGCCGGC",
        location=BarcodeLocationType.THREE_PRIME,
        name="3prime"
    ),
    BarcodeConfig(
        sequence="CTGACTCCTTAAGGGCC",
        location=BarcodeLocationType.FIVE_PRIME,
        name="5prime"
    )
]

# Create configuration
config = BarcodeExtractorConfig(
    barcodes=barcodes,
    output_prefix="my_extraction",
    output_dir="./results",
    max_mismatches=0,
    search_softclipped=True,
    verbose=True
)

# Process BAM file
stats = process_bam_file(config, "tests/test.bam")

# Report results
print(f"Processed {stats.total_reads} reads")
print(f"Found {stats.total_barcode_matches} barcode matches")

or FASTQ files:

from BarcodeSeqKit.fastq_processing import process_fastq_files

# Use the same config as above
fastq_files = ["tests/test.1.fastq.gz", "tests/test.2.fastq.gz"]
stats = process_fastq_files(
    config=config,
    fastq_files=fastq_files,
    compress_output=True,
    search_both_reads=True
)

Key Concepts

Barcode Types

BarcodeSeqKit supports three types of barcode configurations:

1. Generic barcodes: Use these when you just want to find a specific sequence regardless of location
2. 5’ barcodes: Use these when the barcode is expected at the 5’ end of the sequence
3. 3’ barcodes: Use these when the barcode is expected at the 3’ end of the sequence

Barcode Orientations

For each barcode, BarcodeSeqKit tracks two possible orientations:

• Forward (FR): The barcode appears in its specified sequence
• Reverse Complement (RC): The barcode appears as its reverse complement

Softclipped Regions

When working with BAM files, the --search-softclipped option examines only the softclipped portions of reads:

• For forward strand reads (+): Examines the 5’ softclipped region
• For reverse strand reads (-): Examines the 3’ softclipped region

This is especially useful for splice leader sequences in trypanosomatids or where barcodes are clipped during alignment.

Advanced Options

Command-Line Arguments

BarcodeSeqKit offers a range of options to customize your extraction:

Option	Description
--max-mismatches N	Allow up to N mismatches in barcode detection
--search-softclipped	Search in softclipped regions (BAM only)
--search-both-reads	Look for barcodes in both reads of paired FASTQ files
--no-compress	Disable compression for FASTQ output files
--verbose	Enable detailed logging

For a complete list, run barcodeseqkit --help.

Barcode Configuration Files

For complex projects with multiple barcodes, you can use a YAML configuration file:

barcodes:
  - sequence: CTGACTCCTTAAGGGCC
    location: 5
    name: 5prime
    description: 5' barcode for experiment X
  - sequence: TAACTGAGGCCGGC
    location: 3
    name: 3prime
    description: 3' barcode for experiment X

Then use it with:

barcodeseqkit --bam test.bam --barcode-config my_barcodes.yaml --output-prefix config_extraction

In BarcodeSeqKit, when multiple barcodes are provided, the program uses an efficient approach: it parses the input file(s) only once while searching for all barcodes simultaneously during that single pass.

Output Files and Statistics

BarcodeSeqKit generates:

1. Categorized output files: BAM or FASTQ files containing reads matching specific barcode/orientation combinations
2. Statistics in JSON format: Detailed machine-readable statistics
3. Statistics in TSV format: Human-readable tabular statistics

The statistics include: - Total number of reads processed - Total barcode matches found - Match counts by barcode type - Match counts by orientation - Match counts by category - Overall match rate

Statistics-Only Mode

BarcodeSeqKit now supports a “statistics-only” mode that processes files and generates detailed statistics without writing output sequence files. This feature is particularly useful for:

• Quickly analyzing barcode distributions in large datasets
• Performing QC checks before committing to full processing
• Estimating barcode frequencies without using additional disk space
• Benchmarking and optimization tasks

Command-line Usage

To use statistics-only mode from the command line, add the --only-stats flag:

barcodeseqkit --bam sample.bam \
              --barcode5 CTGACTCCTTAAGGGCC \
              --output-prefix quick_stats \
              --output-dir results \
              --only-stats

BarcodeSeqKit has a clean, modular design:

1. Core (00_core.ipynb): Data structures and configuration
2. Sequence Utilities (01_sequence_utils.ipynb): Barcode detection algorithms
3. BAM Processing (02_bam_processing.ipynb): BAM file handling
4. FASTQ Processing (03_fastq_processing.ipynb): FASTQ file handling
5. Command-Line Interface (04_cli.ipynb): Argument parsing and execution

Real-World Example

Let’s walk through a practical example of extracting barcodes from the test data included with BarcodeSeqKit:

from BarcodeSeqKit.core import BarcodeConfig, BarcodeLocationType, BarcodeExtractorConfig
from BarcodeSeqKit.bam_processing import process_bam_file
import os

# Define barcodes that we know are in the test data
barcodes = [
    BarcodeConfig(
        sequence="TAACTGAGGCCGGC",
        location=BarcodeLocationType.THREE_PRIME,
        name="3prime"
    ),
    BarcodeConfig(
        sequence="CTGACTCCTTAAGGGCC",
        location=BarcodeLocationType.FIVE_PRIME,
        name="5prime"
    )
]

# Create configuration
output_dir = "../tests/index_api"
os.makedirs(output_dir, exist_ok=True)

config = BarcodeExtractorConfig(
    barcodes=barcodes,
    output_prefix="example_run",
    output_dir=output_dir,
    max_mismatches=0,
    search_softclipped=True,
    verbose=True
)

# Process the BAM file (if it exists)
test_bam = "../tests/test.bam"
if os.path.exists(test_bam):
    print(f"Processing {test_bam}")
    stats = process_bam_file(config, test_bam)
    
    # Print summary statistics
    print(f"\nResults summary:")
    print(f"Total reads: {stats.total_reads}")
    print(f"Total barcode matches: {stats.total_barcode_matches}")
    
    if stats.total_reads > 0:
        match_rate = (stats.total_barcode_matches / stats.total_reads) * 100
        print(f"Match rate: {match_rate:.2f}%")
    
    # Print barcode-specific statistics
    for barcode_name, count in stats.matches_by_barcode.items():
        print(f"  {barcode_name}: {count} matches")
    
    # Print orientation-specific statistics
    for orientation, count in stats.matches_by_orientation.items():
        print(f"  Orientation {orientation}: {count} matches")
else:
    print(f"Test file not found: {test_bam}")

2025-03-24 14:06:24,292 - BarcodeSeqKit - INFO - BAM file: ../tests/test.bam (498 reads)
2025-03-24 14:06:24,293 - BarcodeSeqKit - INFO - Output categories: ['barcode3_orientFR', 'barcode3_orientRC', 'barcode5_orientFR', 'barcode5_orientRC', 'noBarcode']

Processing ../tests/test.bam

Classifying reads:   0%|          | 0/498 [00:00<?, ?it/s]

2025-03-24 14:06:24,340 - BarcodeSeqKit - INFO - First pass complete: classified 18 reads

Writing reads:   0%|          | 0/498 [00:00<?, ?it/s]

2025-03-24 14:06:24,411 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_api/example_run_barcode3_orientFR.bam
2025-03-24 14:06:24,424 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_api/example_run_barcode3_orientRC.bam
2025-03-24 14:06:24,433 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_api/example_run_barcode5_orientFR.bam
2025-03-24 14:06:24,442 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_api/example_run_barcode5_orientRC.bam
2025-03-24 14:06:24,450 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_api/example_run_noBarcode.bam


Results summary:
Total reads: 498
Total barcode matches: 18
Match rate: 3.61%
  5prime: 10 matches
  3prime: 8 matches
  Orientation FR: 10 matches
  Orientation RC: 8 matches

config = BarcodeExtractorConfig(
    barcodes=barcodes,
    output_prefix="quick_stats",
    output_dir="../tests/quick_stats",
    max_mismatches=0,
    verbose=True,
    write_output_files=False  # Skip writing sequence files
)

# Process BAM file and get statistics only
stats = process_bam_file(config, "../tests/test.bam")

# Print summary
print(f"Total reads: {stats.total_reads}")
print(f"Total barcode matches: {stats.total_barcode_matches}")
print(f"Match rate: {stats.total_barcode_matches / stats.total_reads * 100:.2f}%")

2025-03-24 14:07:19,200 - BarcodeSeqKit - INFO - BAM file: ../tests/test.bam (498 reads)
2025-03-24 14:07:19,202 - BarcodeSeqKit - INFO - Output categories: ['barcode3_orientFR', 'barcode3_orientRC', 'barcode5_orientFR', 'barcode5_orientRC', 'noBarcode']

Classifying reads:   0%|          | 0/498 [00:00<?, ?it/s]

2025-03-24 14:07:19,259 - BarcodeSeqKit - INFO - First pass complete: classified 18 reads

Total reads: 498
Total barcode matches: 18
Match rate: 3.61%

!barcodeseqkit --bam ../tests/test.bam \
              --barcode5 CTGACTCCTTAAGGGCC \
              --barcode3 TAACTGAGGCCGGC \
              --output-prefix dual_barcode \
              --output-dir ../tests/index_cli

Input BAM file: ../tests/test.bam
Using 5' barcode with sequence: CTGACTCCTTAAGGGCC
Using 3' barcode with sequence: TAACTGAGGCCGGC
Saved configuration to ../tests/index_cli/dual_barcode_config.yaml
2025-03-17 12:18:29,756 - BarcodeSeqKit - INFO - BAM file: ../tests/test.bam (498 reads)
2025-03-17 12:18:29,756 - BarcodeSeqKit - INFO - Output categories: ['barcode5_orientFR', 'barcode5_orientRC', 'barcode3_orientFR', 'barcode3_orientRC', 'noBarcode']
Classifying reads: 100%|███████████████████| 498/498 [00:00<00:00, 58040.55it/s]
2025-03-17 12:18:29,810 - BarcodeSeqKit - INFO - First pass complete: classified 18 reads
Writing reads: 100%|██████████████████████| 498/498 [00:00<00:00, 230344.44it/s]
2025-03-17 12:18:29,816 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_cli/dual_barcode_barcode5_orientFR.bam
2025-03-17 12:18:29,844 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_cli/dual_barcode_barcode5_orientRC.bam
2025-03-17 12:18:29,856 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_cli/dual_barcode_barcode3_orientFR.bam
2025-03-17 12:18:29,882 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_cli/dual_barcode_barcode3_orientRC.bam
2025-03-17 12:18:29,894 - BarcodeSeqKit - INFO - Sorting and indexing ../tests/index_cli/dual_barcode_noBarcode.bam
Extraction complete

Conclusion

BarcodeSeqKit provides a streamlined, user-friendly approach to barcode extraction from sequencing data. With its intuitive interface and flexible options, it’s suitable for a wide range of applications, from simple barcode detection to complex multi-barcode analyses.

Whether you’re working with BAM files, FASTQ files, single barcodes, or multiple barcodes with specific locations, BarcodeSeqKit offers a straightforward solution for your barcode extraction needs.

For detailed API documentation, check out the module-specific notebooks: - Core Data Structures - Sequence Utilities - BAM Processing - FASTQ Processing - Command-Line Interface