-
Notifications
You must be signed in to change notification settings - Fork 0
Expand file tree
/
Copy pathmain_survival.py
More file actions
282 lines (237 loc) · 12 KB
/
Copy pathmain_survival.py
File metadata and controls
282 lines (237 loc) · 12 KB
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
276
277
278
279
280
281
from __future__ import print_function
import argparse
import os
from timeit import default_timer as timer
# internal imports
from utils.file_utils import save_pkl
from utils.utils import *
from utils.survival_core_utils import train
from dataset.dataset_survival import Generic_MIL_Survival_Dataset
# pytorch imports
import torch
import pandas as pd
import numpy as np
import wandb
def main(args):
# create results directory if necessary
if 'summary.csv' in os.listdir(args.results_dir):
print("Experiment already done, exiting...")
return
# wandb.init(project=args.task)
# wandb.config.update(args)
if args.k_start == -1:
start = 0
else:
start = args.k_start
if args.k_end == -1:
end = args.k
else:
end = args.k_end
latest_test_cindex = []
latest_val_cindex = []
folds = np.arange(start, end)
for i in folds:
start = timer()
seed_torch(args.seed)
results_pkl_path = os.path.join(args.results_dir, 'split_latest_val_{}_results.pkl'.format(i))
if os.path.isfile(results_pkl_path):
print("Skipping Split %d" % i)
continue
train_dataset, val_dataset, test_dataset = dataset.return_splits(args.backbone, args.patch_size, from_id=False,
csv_path='{}/splits_{}.csv'.format(args.split_dir, i))
if args.k_fold:
print('training: {}, validation: {}'.format(len(train_dataset), len(val_dataset)))
else:
print('training: {}, validation: {}, testing: {}'.format(len(train_dataset), len(val_dataset), len(test_dataset)))
if args.k_fold:
datasets = (train_dataset, val_dataset)
else:
datasets = (train_dataset, val_dataset, test_dataset)
if args.preloading == 'yes':
for d in datasets:
d.pre_loading()
if args.task_type == 'survival':
if args.k_fold:
cindex_val = train(datasets, i, args)
latest_val_cindex.append(cindex_val)
else:
results, cindex_test, cindex_val = train(datasets, i, args)
latest_val_cindex.append(cindex_val)
latest_test_cindex.append(cindex_test)
# results, test_auc, val_auc, test_acc, val_acc = train(datasets, i, args)
# all_test_auc.append(test_auc)
# all_val_auc.append(val_auc)
# all_test_acc.append(test_acc)
# all_val_acc.append(val_acc)
#write results to pkl
filename = os.path.join(args.results_dir, 'split_{}_results.pkl'.format(i))
if not args.k_fold:
save_pkl(filename, results)
if args.k_fold:
final_df = pd.DataFrame({'folds': folds, 'val_cindex': latest_val_cindex})
else:
final_df = pd.DataFrame({'folds': folds, 'test_cindex': latest_test_cindex,
'val_cindex': latest_val_cindex, })
if len(folds) != args.k:
save_name = 'summary_partial_{}_{}.csv'.format(start, end)
else:
save_name = 'summary.csv'
final_df.to_csv(os.path.join(args.results_dir, save_name))
if not args.k_fold:
mean_test = final_df['test_cindex'].mean()
std_test = final_df['test_cindex'].std()
mean_val = final_df['val_cindex'].mean()
std_val = final_df['val_cindex'].std()
if args.k_fold:
df_append = pd.DataFrame({
'folds': ['mean', 'std'],
'val_cindex': [mean_val, std_val]
})
else:
df_append = pd.DataFrame({
'folds': ['mean', 'std'],
'test_cindex': [mean_test, std_test],
'val_cindex': [mean_val, std_val]
})
final_df = pd.concat([final_df, df_append])
if len(folds) != args.k:
save_name = 'summary_partial_{}_{}.csv'.format(start, end)
else:
save_name = 'summary.csv'
final_df.to_csv(os.path.join(args.results_dir, save_name))
final_df['folds'] = final_df['folds'].astype(str)
# table = wandb.Table(dataframe=final_df)
# wandb.log({"summary": table})
# if args.k_fold:
# wandb.log({"mean_val_cindex": mean_val})
# else:
# wandb.log({"mean_test_cindex": mean_test, "mean_val_cindex": mean_val})
# Generic training settings
parser = argparse.ArgumentParser(description='Configurations for WSI Training')
parser.add_argument('--data_root_dir', type=str, default='/home/guestdj/sdc/TCGA_Pancancer/CONCH/TCGA_COADREAD',
help='Data directory to WSI features (extracted via CLAM)')
parser.add_argument('--results_dir', default='./results', help='results directory (default: ./results)')
parser.add_argument('--split_dir', type=str, default='./splits/TCGA_COADREAD',
help='manually specify the set of splits to use')
parser.add_argument('--csv_path', type=str, default='./dataset_csv/TCGA_COADREAD_processed.csv', help='csv file containing the dataset')
parser.add_argument('--model_type', type=str, default='HGP-Mamba', help='type of model')
parser.add_argument('--mode', type = str, choices=['path', 'mIF', 'multi-modal'], default='multi-modal', help='which modalities to use')
parser.add_argument('--fusion', type=str, choices=['None', 'concat', 'IFBlock'], default='IFBlock', help='Type of fusion. (Default: None).')
parser.add_argument('--exp_code', type=str, default='HGPMamba', help='experiment code for saving results')
parser.add_argument('--seed', type=int, default=42, help='random seed for reproducible experiment (default: 1)')
parser.add_argument('--max_epochs', type=int, default=100, help='maximum number of epochs to train (default: 200)')
parser.add_argument('--lr', type=float, default=2e-4, help='learning rate (default: 0.0001)')
parser.add_argument('--drop_out', type=float, default=0.25, help='enable dropout (p=0.25)')
parser.add_argument('--batch_size', type=int, default=1,)
parser.add_argument('--label_frac', type=float, default=1.0, help='fraction of training labels (default: 1.0)')
parser.add_argument('--weighted_sample', action='store_true', default=True, help='enable weighted sampling')
parser.add_argument('--alpha_surv', type=float, default=0.0, help='How much to weigh uncensored patients')
parser.add_argument('--early_stopping', action='store_true', default=True, help='enable early stopping')
parser.add_argument('--opt', type=str, choices = ['adam', 'sgd', 'adamW'], default='adam')
parser.add_argument('--reg', type=float, default=1e-5, help='L2-regularization weight decay (default: 1e-5)')
parser.add_argument('--gc', type=int, default=32, help='Gradient Accumulation Step.')
parser.add_argument('--bag_loss', type=str, choices=['svm', 'ce', 'ce_surv', 'nll_surv', 'cox_surv'], default='nll_surv', help='slide-level classification loss function (default: ce)')
parser.add_argument('--reg_type', type=str, choices=['None', 'L1'], default='None', help='apply Regularization (default: None)')
parser.add_argument('--lambda_reg', type=float, default=1e-4, help='L1-Regularization Strength (Default 1e-4)')
parser.add_argument('--k_fold', type=bool, default=True, help='k fold for cross validation')
parser.add_argument('--k', type=int, default=5, help='number of folds (default: 10)')
parser.add_argument('--k_start', type=int, default=-1, help='start fold (default: -1, last fold)')
parser.add_argument('--k_end', type=int, default=-1, help='end fold (default: -1, first fold)')
parser.add_argument('--log_data', action='store_true', default=True, help='log data using tensorboard')
parser.add_argument('--testing', action='store_true', default=False, help='debugging tool')
parser.add_argument('--apply_sig', action='store_true', default=False, help='Use genomic features as signature embeddings')
parser.add_argument('--apply_sigfeats', action='store_true', default=False, help='Use genomic features as tabular features.')
## CLAM settings
parser.add_argument('--inst_loss', type=str, choices=['svm', 'ce', None], default='ce',
help='instance-level clustering loss function (default: None)')
parser.add_argument('--subtyping', action='store_true', default=True,
help='subtyping problem')
parser.add_argument('--bag_weight', type=float, default=0.7,
help='clam: weight coefficient for bag-level loss (default: 0.7)')
parser.add_argument('--B', type=int, default=8, help='numbr of positive/negative patches to sample for clam')
parser.add_argument('--backbone', type=str, default='conch')
parser.add_argument('--patch_size', type=str, default='512')
parser.add_argument('--preloading', type=str, default='no')
parser.add_argument('--in_dim', type=int, default=512)
## Mamba settings
parser.add_argument('--mambamil_rate',type=int, default=10, help='mambamil_rate')
parser.add_argument('--mambamil_layer',type=int, default=2, help='mambamil_layer')
parser.add_argument('--d_state', type=int, default=16, help='d_state for SSM')
parser.add_argument('--mambamil_type',type=str, default='BiMamba', choices= ['Mamba', 'BiMamba', 'SRMamba'], help='mambamil_type')
args = parser.parse_args()
device=torch.device("cuda" if torch.cuda.is_available() else "cpu")
print('Deviece is:', device)
def seed_torch(seed=7):
import random
random.seed(seed)
os.environ['PYTHONHASHSEED'] = str(seed)
np.random.seed(seed)
torch.manual_seed(seed)
if device.type == 'cuda':
torch.cuda.manual_seed(seed)
torch.cuda.manual_seed_all(seed) # if you are using multi-GPU.
torch.backends.cudnn.benchmark = False
torch.backends.cudnn.deterministic = True
seed_torch(args.seed)
print("Experiment Name:", args.exp_code)
settings = {'num_splits': args.k,
'k_start': args.k_start,
'k_end': args.k_end,
'max_epochs': args.max_epochs,
'results_dir': args.results_dir,
'split_dir': args.split_dir,
'lr': args.lr,
'early_stopping': args.early_stopping,
'experiment': args.exp_code,
'reg': args.reg,
'reg_type': args.reg_type,
'label_frac': args.label_frac,
'bag_loss': args.bag_loss,
'seed': args.seed,
'model_type': args.model_type,
"use_drop_out": args.drop_out,
'weighted_sample': args.weighted_sample,
'opt': args.opt,
'fusion': args.fusion}
if args.reg_type == 'L1':
settings.update({'lambda_reg': args.lambda_reg})
if args.model_type in ['HGPMamba', 'MAMBA_MIL']:
settings.update({'mambamil_rate': args.mambamil_rate,
'mambamil_layer': args.mambamil_layer,
'mamba_type': args.mamba_type,
'd_state': args.d_state})
print('\nLoad Dataset')
args.n_classes = 4
dataset = Generic_MIL_Survival_Dataset(csv_path = args.csv_path,
mode = args.mode,
apply_sig = args.apply_sig,
data_dir= os.path.join(args.data_root_dir),
shuffle = False,
seed = args.seed,
print_info = True,
patient_strat= False,
n_bins=4,
label_col = 'survival_months',
ignore=[])
if isinstance(dataset, Generic_MIL_Survival_Dataset):
args.task_type = 'survival'
else:
raise NotImplementedError
args.results_dir = os.path.join(args.results_dir, str(args.exp_code) + '_s{}'.format(args.seed))
if not os.path.isdir(args.results_dir):
os.makedirs(args.results_dir)
print('split_dir: ', args.split_dir)
assert os.path.isdir(args.split_dir)
settings.update({'split_dir': args.split_dir})
with open(args.results_dir + '/experiment.txt', 'w') as f:
print(settings, file=f)
print("################# Settings ###################")
for key, val in settings.items():
print("{}: {}".format(key, val))
if __name__ == "__main__":
start = timer()
results = main(args)
end = timer()
print("finished!")
print("end script")
print('Script Time: %f seconds' % (end - start))