https://github.com/rguerillot/RM-seq
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Tip revision: 870123e8415d1527e90dfdbd9f544df1b9a392a1 authored by Romain on 16 January 2019, 06:05:04 UTC
Added --noaln option to skip reads alignment when generating consensus reads
Tip revision: 870123e
setup.py
#!/usr/bin/env python3
from setuptools import setup
import RMseq
import os


LONG_DESCRIPTION = 'RM-seq is a bioinformatics tool for assessing resistance mutations from complex or pooled resistant bacterial population using barcoded amplicons sequencing data'

if os.path.exists('README'):
    LONG_DESCRIPTION = open('README').read()

setup(
    name = 'rmseq',
    version = RMseq.__version__,
    description = RMseq.__description__,
    long_description=LONG_DESCRIPTION,
    classifiers = ['Development Status :: 3 - Alpha',
                   'License :: OSI Approved :: GNU Affero General ' +
                   'Public License v3 or later (AGPLv3+)',
                   'Programming Language :: Python :: 3.5',
                   'Topic :: Scientific/Engineering :: Bio-Informatics',
                   'Topic :: Scientific/Engineering :: Medical Science Apps.',
                   'Intended Audience :: Science/Research'],
    keywords = ['resistance',
                'mutation'],
    download_url = RMseq.__download_url__,
    author = RMseq.__author__,
    author_email = RMseq.__author_email__,
    license = RMseq.__license__,
    packages = ['RMseq'],
    scripts = ['RMseq/rmseq',
               'RMseq/amplicon-effect.py',
               'RMseq/RM-seq.pl'],
    include_package_data = True,
    install_requires = ['plumbum>=1.6.3',
                        'biopython>=1.69',
                        'numpy>=1.13.1']
    )
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