Pysam

pysam

Overview

Use pysam for low-level, streaming access to HTSlib-supported genomic formats:

• AlignmentFile and AlignedSegment for SAM/BAM/CRAM
• VariantFile, VariantHeader, and VariantRecord for VCF/BCF
• FastaFile for indexed FASTA and FastxFile for sequential FASTA/FASTQ
• TabixFile for BGZF-compressed, tabix-indexed BED/GFF/GTF/custom tables
• pysam.samtools and pysam.bcftools for wrapped command dispatchers

Current upstream baseline: pysam 0.24.1 (7 September 2026), wrapping HTSlib/samtools/bcftools 1.24. Read references/sources.md before updating version-specific guidance.

Installation

Use the pinned release for reproducible work:

uv pip install "pysam==0.24.1"

Confirm the runtime:

import pysam

print(pysam.__version__)           # 0.24.1
print(pysam.__samtools_version__)  # 1.24

Prebuilt wheels are available for supported macOS and Linux platforms. A source build needs a C compiler and HTSlib build dependencies; read the official installation guide linked from references/sources.md.

First Decide

Before writing code:

1. Identify the real format, compression, sort order, and available index.
2. Decide whether coordinates are numeric Python coordinates or a region string. Do not mix them.
3. For CRAM, identify the exact reference assembly and FASTA.
4. Prefer indexed region access; use sequential iteration only when intended.
5. Preserve headers when writing and write to a new path by default.
6. State filtering semantics: mapping/base quality, flags, overlap handling, duplicate handling, and pileup depth cap.

For unfamiliar files, start with the bundled read-only inspector:

python scripts/inspect_hts.py sample.bam
python scripts/inspect_hts.py cohort.vcf.gz
python scripts/inspect_hts.py reference.fa

Bundled Scripts

All scripts refuse to overwrite existing outputs. The filter also refuses stale output indexes and offers --index --csi for large BAM contigs. FASTA inspection requires an existing .fai; create it explicitly with pysam.faidx() first. Run each with --help for coordinate, index, and privacy notes.

Examples use illustrative filenames and assay-specific thresholds. The local synthetic suite exercises these API patterns on pysam 0.24.1; remote storage and biological datasets are not part of that validation.

Coordinate Contract

Numeric coordinates accepted by pysam APIs are 0-based, half-open. This includes numeric AlignmentFile.fetch(), VariantFile.fetch(), FastaFile.fetch(), TabixFile.fetch(), and pileup() arguments.

Region strings are samtools-style: 1-based and inclusive.

# The same 100 bases:
bam.fetch("chr1", 99, 199)          # [99, 199)
bam.fetch(region="chr1:100-199")    # 1-based inclusive

VCF text uses 1-based POS, while record properties expose both systems:

record.pos    # 1-based
record.start  # 0-based inclusive
record.stop   # 0-based exclusive

Read references/coordinates_and_indexing.md for format conversions, overlap semantics, index choices, and contig-name checks.

Alignment Files

Use context managers and explicit modes:

import pysam

with pysam.AlignmentFile("sample.bam", "rb", threads=4) as bam:
    for read in bam.fetch("chr1", 1_000, 2_000):
        if (
            not read.is_unmapped
            and not read.is_secondary
            and not read.is_supplementary
            and read.mapping_quality >= 30
        ):
            print(read.query_name, read.reference_start, read.cigarstring)

Use fetch(until_eof=True) to stream every record in file order, including unplaced unmapped reads, without requiring an index:

with pysam.AlignmentFile("sample.bam", "rb") as bam:
    for read in bam.fetch(until_eof=True):
        ...

Important distinctions:

• fetch() returns placed alignment records overlapping a region; even an unmapped-flagged record can have a reference position. Filter is_unmapped.
• count() counts records and defaults to read_callback="nofilter".
• count_coverage() returns A/C/G/T base counts and defaults to base quality 15 plus read_callback="all".
• pileup() exposes per-column reads and has its own filtering, base-quality, overlap, orphan, and max_depth=8000 defaults.

For exact-region pileups, set truncate=True and explicit filters:

with pysam.FastaFile("reference.fa") as fasta, pysam.AlignmentFile(
    "sample.bam", "rb"
) as bam:
    for column in bam.pileup(
        "chr1",
        1_000,
        2_000,
        truncate=True,
        stepper="samtools",
        fastafile=fasta,
        min_mapping_quality=20,
        min_base_quality=20,
        max_depth=100_000,
    ):
        base_depth = sum(
            not item.is_del and not item.is_refskip
            and item.query_position is not None
            for item in column.pileups
        )
        print(column.reference_pos, base_depth)

Read references/alignment_files.md for flags, CIGAR operations, tags, modified bases, writing records, pileup details, and iterator lifetime.

Variant Files

Input format is auto-detected. Numeric fetch coordinates remain 0-based:

import pysam

with pysam.VariantFile("cohort.vcf.gz", threads=4) as variants:
    for record in variants.fetch("chr1", 999_999, 2_000_000):
        print(record.contig, record.pos, record.ref, record.alts)
        for sample_name, call in record.samples.items():
            print(sample_name, call.get("GT"))

Subset samples before retrieving records:

with pysam.VariantFile("cohort.bcf") as variants:
    variants.subset_samples(["sample_A", "sample_B"])
    for record in variants:
        ...

When changing a header, copy each record and translate it to the destination header before assigning newly declared INFO/FORMAT/FILTER fields. Do not manually clear and rebuild header.samples.

Read references/variant_files.md for safe headers, writing, sample subsetting, missing genotypes, symbolic alleles, filtering, translation, and indexing.

FASTA, FASTQ, and Tabix

Indexed FASTA uses numeric 0-based coordinates:

with pysam.FastaFile("reference.fa") as fasta:
    sequence = fasta.fetch("chr1", 999, 1_099)

FastxFile is sequential. persist=False is faster but yielded records become invalid after iteration advances:

with pysam.FastxFile("reads.fastq.gz", persist=False) as reads:
    for read in reads:
        qualities = read.get_quality_array()
        ...

Tabix input must be coordinate-sorted and BGZF-compressed, not ordinary gzip. Use a non-destructive two-step workflow:

pysam.tabix_compress("regions.bed", "regions.bed.gz")
pysam.tabix_index("regions.bed.gz", preset="bed")

with pysam.TabixFile("regions.bed.gz", parser=pysam.asBed()) as tbx:
    for interval in tbx.fetch("chr1", 1_000, 2_000):
        print(interval.contig, interval.start, interval.end)

Read references/sequence_files.md for FASTA/FASTQ records and safe tabix creation.

CRAM, Remote I/O, and Threads

pysam 0.24 changed inherited HTSlib behavior:

• Newly written CRAM defaults to CRAM 3.1, not 3.0.
• HTSlib no longer contacts the EBI reference server by default.
• Prefer reference_filename="reference.fa" for deterministic local reads and writes.

with pysam.AlignmentFile(
    "sample.cram",
    "rc",
    reference_filename="reference.fa",
    threads=4,
) as cram:
    for read in cram.fetch("chr1", 1_000, 2_000):
        ...

Only configure REF_PATH/REF_CACHE when reference-by-MD5 lookup is intentional. Do not assume a CRAM is self-contained. threads= accelerates compression/decompression; it does not parallelize Python analysis.

Read references/cram_and_performance.md before CRAM conversion, remote access, or concurrent iteration.