- Author
Andreas Heger, John Marshall, Kevin Jacobs, and contributors
- Date
- Version
Pysam is a python module for reading, manipulating and writing genomic data sets.
Pysam is a wrapper of the htslib C-API and provides facilities to read and write SAM/BAM/VCF/BCF/BED/GFF/GTF/FASTA/FASTQ files as well as access to the command line functionality of the samtools and bcftools packages. The module supports compression and random access through indexing.
This module provides a low-level wrapper around the htslib C-API as using cython and a high-level, pythonic API for convenient access to the data within genomic file formats.
The current version wraps htslib-1.18, samtools-1.18, and bcftools-1.18.
To install the latest release, type:
pip install pysam
See the Installation notes <installation>
for details.
This module is unrelated to NREL-PySAM, which wraps the National Renewable Energy Laboratory's System Advisor Model.
api.rst usage.rst installation.rst faq.rst developer.rst release.rst benchmarking.rst glossary.rst
Contents:
genindex
modindex
search
- Information about htslib
- The samtools homepage
- The cython C-extensions for python
- The python language
- Bonfield.2021
HTSlib: C library for reading/writing high-throughput sequencing data. Bonfield JK, Marshall J, Danecek P, Li H, Ohan V, Whitwham A, Keane T, Davies RM. GigaScience (2021) 10(2) giab007. PMID: 33594436.
- Danecek.2021
Twelve years of SAMtools and BCFtools. Danecek P, Bonfield JK, Liddle J, Marshall J, Ohan V, Pollard MO, Whitwham A, Keane T, McCarthy SA, Davies RM, Li H. GigaScience (2021) 10(2) giab008. PMID: 33590861.
- Li.2009
The Sequence Alignment/Map format and SAMtools. Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R; 1000 Genome Project Data Processing Subgroup. Bioinformatics. 2009 Aug 15;25(16):2078-9. Epub 2009 Jun 8 btp352. PMID: 19505943.