bwamem 0.0.15

Bindings to bwa aligner

bwamem

Python bindings for the BWA-MEM aligner.

Installation

pip install bwamem

Usage

Build Index

from bwamem import BwaIndexer

indexer = BwaIndexer()
index_path = indexer.build_index('reference.fa')

Single-End Alignment

from bwamem import BwaAligner

aligner = BwaAligner('path/to/index')
alignments = aligner.align('ACGATCGCGATCGA')

for aln in alignments:
    print(f'{aln.ctg}:{aln.r_st} strand={aln.strand} mapq={aln.mapq}')

Paired-End Alignment

read1 = 'ACGATCGCGATCGA'
read2 = 'TTCGATCGATCGAT'

paired_alignments = aligner.align(read1, read2)

for pe_aln in paired_alignments:
    print(f'Insert size: {pe_aln.insert_size}, Proper pair: {pe_aln.is_proper_pair}')

Retrieve Sequences from Index

# Get full sequence
seq = aligner.seq('chr1')

# Get subsequence
subseq = aligner.seq('chr1', start=100, end=200)

Monitor Index Building Progress

from bwamem import BwaIndexer

indexer = BwaIndexer()
# Progress messages are captured by default (no console spam)
index_path = indexer.build_index('genome.fasta')

# Check progress info
progress = indexer.get_progress()
print(f"Status: {progress['status']}")
print(f"Iterations: {progress['iterations']}")
print(f"Characters processed: {progress['characters_processed']}")

# Get progress percentage (if available)
if indexer.progress_percent:
    print(f"Progress: {indexer.progress_percent:.1f}%")

# Access all captured messages
for msg in progress['messages']:
    print(msg)

Control Index Building Verbosity

from bwamem import BwaIndexer

indexer = BwaIndexer()

# Verbosity levels:
# 0 = silent (no output)
# 1 = quiet (only warnings/errors) - default
# 2 = normal (standard BWA messages)
# 3+ = debug (verbose output)

# Silent mode
indexer.build_index('genome.fasta', verbose=0)

# Normal mode with progress messages shown in console
indexer.build_index('genome.fasta', verbose=2, capture_progress=False)

# Debug mode
indexer.build_index('genome.fasta', verbose=3)

Read FASTA/FASTQ Files

from bwamem import fastx_read, read_paired_fastx

# Single-end (supports both FASTA and FASTQ)
for read in fastx_read('sequences.fasta.gz'):
    print(f'{read.name}: {read.sequence}')

# Paired-end
for read1, read2 in read_paired_fastx('R1.fastq', 'R2.fastq'):
    print(f'{read1.name}, {read2.name}')

Custom Options

# Specify alignment parameters
aligner = BwaAligner('path/to/index', options='-x ont2d -A 1 -B 0')

# Set custom insert size for paired-end reads
aligner = BwaAligner('path/to/index', insert_model=(500, 50))
paired_alignments = aligner.align(read1, read2)

Alignment Attributes

Each Alignment object contains the following attributes:

Attribute	Description
ctg	Contig/reference name
r_st	Reference start position (0-based)
r_en	Reference end position (property)
strand	Strand: +1 for forward, -1 for reverse
q_st, q_en	Query start/end positions
mapq	Mapping quality score
cigar	CIGAR as list of [length, op] pairs
cigar_str	CIGAR string (property)
NM	Edit distance
score	Alignment score
is_primary	Primary alignment flag

Calculated properties (computed on demand): r_en, cigar_str, blen, mlen

CIGAR operations: 0=M (match), 1=I (insertion), 2=D (deletion), 3=N (skip), 4=S (soft-clip), 5=H (hard-clip)

PairedAlignment contains: read1, read2 (Alignment objects), is_proper_pair (bool), insert_size (int or None)

License

• Python bindings: Mozilla Public License 2.0
• BWA: GNU General Public License v3.0