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setup.py
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from setuptools import setup
setup(
name="vatools",
version="5.1.0",
packages=["vatools"],
entry_points={
"console_scripts":[
"vcf-expression-annotator = vatools.vcf_expression_annotator:main",
"vcf-readcount-annotator = vatools.vcf_readcount_annotator:main",
"vcf-info-annotator = vatools.vcf_info_annotator:main",
"vcf-genotype-annotator = vatools.vcf_genotype_annotator:main",
"vep-annotation-reporter = vatools.vep_annotation_reporter:main",
"transform-split-values = vatools.transform_split_values:main",
"ref-transcript-mismatch-reporter = vatools.ref_transcript_mismatch_reporter:main",
]
},
install_requires=[
'vcfpy==0.12.3',
'pysam',
'pandas',
'gtfparse==1.3.0',
'testfixtures',
],
classifiers=[
'Development Status :: 5 - Production/Stable',
'Intended Audience :: Science/Research',
'Topic :: Scientific/Engineering :: Bio-Informatics',
"Programming Language :: Python :: 3.5",
'License :: OSI Approved :: MIT License',
],
author = 'Susanna Kiwala, Chris Miller',
author_email = "[email protected]",
description = "A tool for annotating VCF files with expression and readcount data",
license = "MIT License",
keywords = "cancer sequencing variant variants gene expression readcounts VAF allele frequency FPKM TPM transcript VCF",
#This needs to be the url where the code is being hosted
url = "https://github.com/griffithlab/vatools",
)