testing combining df script
This commit is contained in:
parent
262bd79204
commit
a220288c5f
1 changed files with 231 additions and 0 deletions
231
scripts/combining_test.py
Executable file
231
scripts/combining_test.py
Executable file
|
@ -0,0 +1,231 @@
|
|||
#!/usr/bin/env python3
|
||||
# -*- coding: utf-8 -*-
|
||||
'''
|
||||
Created on Tue Aug 6 12:56:03 2019
|
||||
|
||||
@author: tanu
|
||||
'''
|
||||
# FIXME: change filename 2(mcsm normalised data)
|
||||
# to be consistent like (pnca_complex_mcsm_norm.csv) : changed manually, but ensure this is done in the mcsm pipeline
|
||||
#=======================================================================
|
||||
# Task: combine 2 dfs with aa position as linking column
|
||||
|
||||
# Input: 2 dfs
|
||||
# <gene.lower()>_complex_mcsm_norm.csv
|
||||
# <gene.lower()>_foldx.csv
|
||||
|
||||
# Output: .csv of all 2 dfs combined
|
||||
|
||||
# useful link
|
||||
# https://stackoverflow.com/questions/23668427/pandas-three-way-joining-multiple-dataframes-on-columns
|
||||
#=======================================================================
|
||||
#%% load packages
|
||||
import sys, os
|
||||
import pandas as pd
|
||||
import numpy as np
|
||||
#from varname import nameof
|
||||
import argparse
|
||||
from combining import combine_stability_dfs
|
||||
from combining import detect_common_cols
|
||||
#=======================================================================
|
||||
#%% specify input and curr dir
|
||||
homedir = os.path.expanduser('~')
|
||||
|
||||
# set working dir
|
||||
os.getcwd()
|
||||
os.chdir(homedir + '/git/LSHTM_analysis/scripts')
|
||||
os.getcwd()
|
||||
#=======================================================================
|
||||
#%% command line args
|
||||
#arg_parser = argparse.ArgumentParser()
|
||||
#arg_parser.add_argument('-d', '--drug', help='drug name', default = 'pyrazinamide')
|
||||
#arg_parser.add_argument('-g', '--gene', help='gene name', default = 'pncA') # case sensitive
|
||||
#args = arg_parser.parse_args()
|
||||
#=======================================================================
|
||||
#%% variable assignment: input and output
|
||||
drug = 'pyrazinamide'
|
||||
gene = 'pncA'
|
||||
gene_match = gene + '_p.'
|
||||
|
||||
#drug = args.drug
|
||||
#gene = args.gene
|
||||
#======
|
||||
# dirs
|
||||
#======
|
||||
datadir = homedir + '/' + 'git/Data'
|
||||
indir = datadir + '/' + drug + '/' + 'input'
|
||||
outdir = datadir + '/' + drug + '/' + 'output'
|
||||
|
||||
#=======
|
||||
# input
|
||||
#=======
|
||||
#in_filename_linking = gene.lower() + '_linking_df.csv'
|
||||
#in_filename_mcsm = gene.lower() + '_complex_mcsm_norm.csv'
|
||||
#in_filename_foldx = gene.lower() + '_foldx.csv'
|
||||
in_filename_dssp = gene.lower() + '_dssp.csv'
|
||||
in_filename_kd = gene.lower() + '_kd.csv'
|
||||
#in_filename_rd = gene.lower() + '_rd.csv'
|
||||
in_filename_snpinfo = 'ns' + gene.lower() + '_snp_info.csv'
|
||||
in_filename_afor = gene.lower() + '_af_or.csv'
|
||||
in_filename_afor_kin = gene.lower() + '_af_or_kinship.csv'
|
||||
|
||||
|
||||
#infile_linking = outdir + '/' + in_filename_linking
|
||||
#infile_mcsm = outdir + '/' + in_filename_mcsm
|
||||
#infile_foldx = outdir + '/' + in_filename_foldx
|
||||
infile_dssp = outdir + '/' + in_filename_dssp
|
||||
infile_kd = outdir + '/' + in_filename_kd
|
||||
#infile_rd = outdir + '/' + in_filename_rd
|
||||
infile_snpinfo = indir + '/' + in_filename_snpinfo
|
||||
infile_afor = outdir + '/' + in_filename_afor
|
||||
infile_afor_kin = outdir + '/' + in_filename_afor_kin
|
||||
|
||||
|
||||
print('\nInput path:', outdir
|
||||
# , '\nInput filename1:', infile_mcsm
|
||||
# , '\nInput filename2:', infile_foldx
|
||||
, '\nInput filename2:', infile_dssp
|
||||
, '\nInput filename2:', infile_kd
|
||||
# , '\nInput filename2:', infile_rd
|
||||
, '\nInput filename snp info:', infile_snpinfo
|
||||
, '\nInput filename af or:', infile_afor
|
||||
, '\nInput filename afor kinship:', infile_afor_kin
|
||||
, '\n============================================================')
|
||||
|
||||
#=======
|
||||
# output
|
||||
#=======
|
||||
#out_filename_comb = gene.lower() + '_struct_params_TEST.csv'
|
||||
#outfile_comb = outdir + '/' + out_filename_comb
|
||||
#print('Output filename:', outfile_comb
|
||||
# , '\n============================================================')
|
||||
|
||||
o_join = 'outer'
|
||||
l_join = 'left'
|
||||
r_join = 'right'
|
||||
i_join = 'inner'
|
||||
|
||||
|
||||
#del(in_filename_dssp, in_filename_foldx)
|
||||
# end of variable assignment for input and output files
|
||||
|
||||
#=======================================================================
|
||||
# call function to detect common cols
|
||||
#=======================================================================
|
||||
def main():
|
||||
|
||||
print('Reading input files:')
|
||||
|
||||
#dssp_df = pd.read_csv(infile_dssp, sep = ',')
|
||||
#dssp_df.columns = dssp_df.columns.str.lower()
|
||||
|
||||
#kd_df = pd.read_csv(infile_kd, sep = ',')
|
||||
#kd_df.columns = kd_df.columns.str.lower()
|
||||
|
||||
# print('Dimension left df:', dssp_df.shape
|
||||
# , '\nDimension right_df:', kd_df.shape
|
||||
# , '\njoin type:', o_join
|
||||
# , '\n=========================================================')
|
||||
|
||||
# detect common cols
|
||||
#merging_cols = detect_common_cols(dssp_df, kd_df)
|
||||
#print('Length of common cols:', len(merging_cols)
|
||||
# , '\nmerging column/s:', merging_cols, 'type:', type(merging_cols)
|
||||
# , '\ndtypes in merging columns:', dssp_df[merging_cols].dtypes)
|
||||
|
||||
#combined_df1 = combine_stability_dfs(dssp_df, kd_df, my_join = o_join)
|
||||
#print('Dimensions of combined df:', combined_df1.shape
|
||||
# , '\nsneak peak:', combined_df1.head()
|
||||
# , '\ndtypes in cols:\n', combined_df1.dtypes)
|
||||
|
||||
#=============================================================================
|
||||
afor_df = pd.read_csv(infile_afor, sep = ',')
|
||||
afor_df.columns = afor_df.columns.str.lower()
|
||||
|
||||
snpinfo_df = pd.read_csv(infile_snpinfo, sep = ',')
|
||||
snpinfo_df.columns = snpinfo_df.columns.str.lower()
|
||||
|
||||
# print('Dimension df1:', afor_df.shape
|
||||
# , '\nDimension df2:', snpinfo_df.shape
|
||||
# , '\njoin type:', l_join
|
||||
# , '\n=========================================================')
|
||||
|
||||
|
||||
# detect common cols
|
||||
merging_cols = detect_common_cols(afor_df, snpinfo_df)
|
||||
#print('Length of common cols:', len(merging_cols)
|
||||
# , '\nmerging column/s:', merging_cols, 'type:', type(merging_cols)
|
||||
# , '\ndtypes in merging columns:', snpinfo_df[merging_cols].dtypes)
|
||||
|
||||
comb_afor_snpinfo = combine_stability_dfs(afor_df, snpinfo_df, my_join = l_join)
|
||||
#print('Dimensions of combined df:', comb_afor_snpinfo.shape
|
||||
# , '\nsneak peak:', comb_afor_snpinfo.head()
|
||||
# , '\ndtypes in cols:\n', comb_afor_snpinfo.dtypes)
|
||||
|
||||
#=============================================================================
|
||||
afor_kin_df = pd.read_csv(infile_afor_kin, sep = ',')
|
||||
afor_kin_df.columns = afor_kin_df.columns.str.lower()
|
||||
|
||||
# detect common cols
|
||||
merging_cols = detect_common_cols(comb_afor_snpinfo, afor_kin_df)
|
||||
|
||||
# comb2 = combine_stability_dfs(comb_afor_snpinfo, afor_kin_df, my_join = o_join)
|
||||
#print('Dimensions of combined df:', comb2.shape
|
||||
# , '\nsneak peak:', comb2.head()
|
||||
# , '\ndtypes in cols:\n', comb2.dtype)
|
||||
|
||||
|
||||
if __name__ == '__main__':
|
||||
main()
|
||||
#=======================================================================
|
||||
#%% end of script
|
||||
#hardocoded test
|
||||
|
||||
dssp_df = pd.read_csv(infile_dssp, sep = ',')
|
||||
kd_df = pd.read_csv(infile_kd, sep = ',')
|
||||
|
||||
afor_df = pd.read_csv(infile_afor, sep = ',')
|
||||
snpinfo_df = pd.read_csv(infile_snpinfo, sep = ',')
|
||||
afor_kin_df = pd.read_csv(infile_afor_kin, sep = ',')
|
||||
|
||||
merging_cols = ['alt_allele',
|
||||
'chr_num_allele',
|
||||
'chromosome_number',
|
||||
'gene_id',
|
||||
'gene_number',
|
||||
'mut_info',
|
||||
'mut_region',
|
||||
'mut_type',
|
||||
'mutant_type',
|
||||
'mutationinformation',
|
||||
'position',
|
||||
'ref_allele',
|
||||
'wild_type']
|
||||
|
||||
print('doing thing')
|
||||
|
||||
|
||||
comb_afor_snpinfo = pd.merge(afor_df, snpinfo_df, on = 'mutation', how = 'inner')
|
||||
comb2 = pd.merge(comb_afor_snpinfo, afor_kin_df, on = merging_cols, how = i_join)
|
||||
comb3 = comb2.drop_duplicates(subset=merging_cols, keep = 'first')
|
||||
|
||||
common = np.intersect1d(comb_afor_snpinfo['mutationinformation'], afor_kin_df['mutationinformation'])
|
||||
|
||||
print('comb3 dim:', comb3.shape
|
||||
, '\ncomb2 dim:', comb2.shape
|
||||
, '\ndim of df1:', comb_afor_snpinfo.shape
|
||||
, '\ndim of df2:', afor_kin_df.shape
|
||||
, '\ncommon vals:', len(common))
|
||||
|
||||
print('expected:\n')
|
||||
|
||||
|
||||
|
||||
|
||||
bar = combine_stability_dfs(comb_afor_snpinfo, afor_kin_df, my_join = o_join)
|
||||
print('XXXXXX\n:', bar.shape)
|
||||
|
||||
#bar = np.intersect1d(comb_afor_snpinfo[merging_cols[0]], afor_kin_df[merging_cols[0]])
|
||||
#print('common values:',len(bar))
|
||||
#comb2 = combine_stability_dfs(comb_afor_snpinfo, afor_kin_df, my_join = o_join)
|
||||
print ('thing finished')
|
Loading…
Add table
Add a link
Reference in a new issue