Pysam
Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtools, bcftools, and tabix.
Install / Use
/learn @pysam-developers/PysamREADME
===== Pysam
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Pysam is a python module for reading and manipulating files in the
SAM/BAM format. The SAM/BAM format is a way to store efficiently large
numbers of alignments (Li 2009_), such as those routinely created by
next-generation sequencing methods.
Pysam is a lightweight wrapper of the samtools_ C-API. Pysam also includes an interface for tabix_.
If you are using the conda packaging manager (e.g. miniconda or anaconda),
you can install pysam from the bioconda channel <https://bioconda.github.io/>_::
conda config --add channels bioconda conda config --add channels conda-forge conda config --set channel_priority strict conda install pysam
Installation through bioconda is the recommended way to install pysam as it resolves non-python dependencies and uses pre-configured compilation options. Especially for OS X this will potentially save a lot of trouble.
The current version of pysam wraps 3rd-party code from htslib-1.23.1, samtools-1.23.1, and bcftools-1.23.1.
Pysam is available through PyPI <https://pypi.org/project/pysam/>_.
To install, type::
pip install pysam
Pysam documentation is available
here <http://pysam.readthedocs.org/en/latest/>_
Questions and comments are very welcome and should be sent to the
pysam user group <http://groups.google.com/group/pysam-user-group>_
.. _samtools: http://samtools.sourceforge.net/ .. _tabix: http://samtools.sourceforge.net/tabix.shtml .. _Li 2009: http://www.ncbi.nlm.nih.gov/pubmed/19505943
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