pysam
CommunityGenomic I/O toolkit for BAM/VCF/FASTA, with tabix and pileup.
Authorovachiever
Version1.0.0
Installs0
System Documentation
What problem does it solve?
Pysam provides Python bindings to htslib for efficient reading, writing, and querying of SAM/BAM/CRAM, VCF/BCF, FASTA/FASTQ, plus indexing and pileup analyses, enabling robust NGS pipelines.
Core Features & Use Cases
- Read/write BAM/CRAM/SAM: Access alignments, fetch regions, and compute coverage.
- Variant handling: Query and process VCF/BCF data; count and annotate variants.
- Sequence access: Random access to indexed reference sequences via FastaFile.
- Workflows: End-to-end pipelines combining alignment, variant, and sequence data.
Quick Start
Open a BAM file, fetch reads in a region, and fetch a FASTA sequence from the reference.
Dependency Matrix
Required Modules
pysam
Components
references
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