https://github.com/rguerillot/RM-seq
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
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']
)