WARNING: This code is an alpha release and not production-ready. APIs may change at any time.
Veppy is a genetic variant effect predictor for Python. Inspired by SnpEff and VEP.
$ pip install veppy
$ git clone firstname.lastname@example.org:solvebio/veppy.git $ cd veppy $ python setup.py install
Step 1 (OPTIONAL): Prepare a directory for veppy data
The default data path is: ./data
You can override this by setting $VEPPY_DATA_DIR.
Step 2: Download source data and build indexes
NOTE: This step downloads about 1gb of data. After indexing, the data directory will consume about 8gb of disk space.
Step 3: Index the source data
>>> from veppy.veppy import calculate_consequences >>> variant = ('1', 8025384, 'A', 'T') >>> result = calculate_consequences('GRCh37', *variant) >>> print result.results
Tests are currently based on chr1 versions of input data. Full genome tests are coming soon!
$ nosetests --with-coverage --cover-package=veppy
TODO: Figure out how to actually get changelog content.
Changelog content for this version goes here.