142 lines
4.6 KiB
Python
142 lines
4.6 KiB
Python
import pandas as pd
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import os, sys
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import numpy as np
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from sklearn.datasets import load_boston
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from sklearn.ensemble import RandomForestRegressor
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from sklearn.model_selection import train_test_split
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from sklearn.feature_selection import RFECV
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import matplotlib.pyplot as plt
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###############################################################################
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homedir = os.path.expanduser("~")
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sys.path.append(homedir + '/git/LSHTM_analysis/scripts/ml/ml_functions')
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sys.path
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# import
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from GetMLData import *
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from SplitTTS import *
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from MultClfs import *
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#from MultClfs_SIMPLE import *
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#%%
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rs = {'random_state': 42}
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skf_cv = StratifiedKFold(n_splits = 10
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, shuffle = True,**rs)
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#sel_cv = logo
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# sel_cv = RepeatedStratifiedKFold(n_splits = 5
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# , n_repeats = 3
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# , **rs)
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# param dict for getmldata()
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gene_model_paramD = {'data_combined_model' : False
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, 'use_or' : False
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, 'omit_all_genomic_features': False
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, 'write_maskfile' : False
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, 'write_outfile' : False }
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#df = getmldata(gene, drug, **gene_model_paramD)
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#df = getmldata('pncA', 'pyrazinamide', **gene_model_paramD)
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df = getmldata('embB', 'ethambutol' , **gene_model_paramD)
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#df = getmldata('katG', 'isoniazid' , **gene_model_paramD)
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#df = getmldata('rpoB', 'rifampicin' , **gene_model_paramD)
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#df = getmldata('gid' , 'streptomycin' , **gene_model_paramD)
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#df = getmldata('alr' , 'cycloserine' , **gene_model_paramD)
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all(df.columns.isin(['gene_name'])) # should be False
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spl_type = '70_30'
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#spl_type = '80_20'
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#spl_type = 'sl'
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#data_type = "actual"
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data_type = "complete"
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df2 = split_tts(df
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, data_type = data_type
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, split_type = spl_type
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, oversampling = True
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, dst_colname = 'dst'
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, target_colname = 'dst_mode'
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, include_gene_name = True
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, random_state = 42 # default
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)
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all(df2['X'].columns.isin(['gene_name'])) # should be False
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df['dst'].value_counts()
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df['dst'].isna().sum()
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df['dst_mode'].value_counts()
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len(df)
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Counter(df2['y'])
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Counter(df2['y_bts'])
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fooD = MultModelsCl(input_df = df2['X']
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, target = df2['y']
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, sel_cv = skf_cv
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, run_blind_test = True
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, blind_test_df = df2['X_bts']
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, blind_test_target = df2['y_bts']
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, tts_split_type = spl_type
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, resampling_type = 'XXXX' # default
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, var_type = ['mixed']
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, scale_numeric = ['min_max']
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, return_formatted_output = False
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)
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for k, v in fooD.items():
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print('\nModel:', k
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, '\nTRAIN MCC:', fooD[k]['test_mcc']
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, '\nBTS MCC:' , fooD[k]['bts_mcc']
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, '\nDIFF:',fooD[k]['bts_mcc'] - fooD[k]['test_mcc'] )
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for k, v in fooD.items():
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print('\nModel:', k
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, '\nTRAIN ACCURACY:', fooD[k]['test_accuracy']
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, '\nBTS ACCURACY:' , fooD[k]['bts_accuracy']
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, '\nDIFF:',fooD[k]['bts_accuracy'] - fooD[k]['test_accuracy'] )
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#%% CHECK SCALING
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embb_df = getmldata('embB', 'ethambutol' , **combined_model_paramD)
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all(embb_df.columns.isin(['gene_name'])) # should be False
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scaler = MinMaxScaler(feature_range=(-1, 1))
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bar = embb_df[['vdwclashes_rr', 'electro_rr']]
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bar_df1 = scaler.fit_transform(bar)
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bar_df1 = pd.DataFrame(bar_df1)
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bar_df1.rename(columns = {0:'vdw_scaled', 1: 'ele_scaled'}, inplace = True)
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bar2 = pd.concat([bar, bar_df1], axis = 1)
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scaler2 = StandardScaler()
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baz = embb_df[['vdwclashes_rr', 'electro_rr']]
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baz_df1 = scaler2.fit_transform(baz)
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baz_df1 = pd.DataFrame(baz_df1)
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baz_df1.rename(columns = {0:'vdw_scaled', 1: 'ele_scaled'}, inplace = True)
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baz2 = pd.concat([baz, baz_df1], axis = 1)
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a = pd.concat([bar2, baz2], axis = 1)
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#%% test added split_types i.e none_with_bts and none_only
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spl_type = 'none_only'
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spl_type = 'none_with_bts'
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spl_type = 'rt'
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#data_type = "actual"
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data_type = "complete"
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df2 = split_tts(df
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, data_type = data_type # only works with complete despite what you set to
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, split_type = spl_type
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, oversampling = True
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, dst_colname = 'dst'
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, target_colname = 'dst_mode'
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, include_gene_name = True
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, random_state = 42 # default
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)
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all(df2['X'].columns.isin(['gene_name'])) # should be False
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import pandas as pd
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from sklearn.utils import all_estimators
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all_clfs = all_estimators(type_filter="classifier")
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df = pd.DataFrame (all_clfs, columns = ['classifier_name', 'classifier_fn'])
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df.to_csv("Model_names_ALL.csv")
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