SleepMaMi / data /shhs_preprocess.py
KeondoPark
Inference code added
a015518
Raw History Blame Contribute Delete
16.1 kB
import os
import shutil
import numpy as np
import matplotlib.pyplot as plt
from tqdm import tqdm
import shutil
import librosa
from scipy.signal import iirnotch, lfilter
from data_utils import butter_bandpass_filter, correct_ecg_inversion
import pickle
import pandas as pd
BASE_PATH = os.path.join(os.path.dirname(os.path.dirname(os.path.abspath(__file__))), 'datasets')
NOTCH_FREQ = 60
EEG_LOWCUT = 0.3
EEG_HIGHCUT = 40
EMG_LOWCUT = 10
EMG_HIGHCUT = 1000
ECG_LOWCUT = 0.3
ECG_HIGHCUT = 60
FLOW_LOWCUT = 0
FLOW_HIGHCUT = 15
NUM_PROCESS = 4
import argparse
import multiprocessing
TARGET_RESAMPLE = 100
def process_ecg(args):
sig, chn_grp, chn = args
sig_path = os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn, sig)
data = np.load(sig_path)
sampling_rate = data.shape[1] // (30)
data = data.reshape(-1, 1)
# Apply bandpass filter
filtered = butter_bandpass_filter(data, ECG_LOWCUT, ECG_HIGHCUT, sampling_rate)
b_notch, a_notch = iirnotch(NOTCH_FREQ, 30, sampling_rate)
filtered = lfilter(b_notch, a_notch, filtered)
filtered = filtered.reshape(-1, sampling_rate*30)
# filtered = librosa.resample(filtered, orig_sr=SAMPLING_RATE, target_sr=TARGET_RESAMPLE, axis=0, res_type='soxr_qq')
filtered_epochs = []
for epoch in filtered:
inv_epoch, _ = correct_ecg_inversion(epoch, TARGET_RESAMPLE)
filtered_epochs.append(inv_epoch)
filtered = np.stack(filtered_epochs, axis=0)
if sampling_rate != TARGET_RESAMPLE:
filtered = np.reshape(filtered, (-1,1))
filtered = librosa.resample(filtered, orig_sr=sampling_rate, target_sr=TARGET_RESAMPLE, axis=0, res_type='soxr_qq')
filtered = filtered.reshape(-1, TARGET_RESAMPLE*30)
if cfg.save_type == 'npy':
# Save processed data
output_path = os.path.join(BASE_PATH, cfg.output_dir, chn_grp, chn, sig)
os.makedirs(os.path.dirname(output_path), exist_ok=True)
np.save(output_path, filtered.astype(np.float32))
return
else:
return filtered
def process_eeg(args):
sig, chn_grp, chn = args
sig_path = os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn, sig)
data = np.load(sig_path)
sampling_rate = data.shape[1] // (30)
data = data.reshape(-1, 1)
# Apply bandpass filter
filtered = butter_bandpass_filter(data, EEG_LOWCUT, EEG_HIGHCUT, sampling_rate)
b_notch, a_notch = iirnotch(NOTCH_FREQ, 30, sampling_rate)
filtered = lfilter(b_notch, a_notch, filtered)
if sampling_rate != TARGET_RESAMPLE:
filtered = librosa.resample(filtered, orig_sr=sampling_rate, target_sr=TARGET_RESAMPLE, axis=0, res_type='soxr_qq')
filtered = filtered.reshape(-1, TARGET_RESAMPLE*30)
if cfg.save_type == 'npy':
# Save processed data
output_path = os.path.join(BASE_PATH, cfg.output_dir, chn_grp, chn, sig)
os.makedirs(os.path.dirname(output_path), exist_ok=True)
np.save(output_path, filtered.astype(np.float32))
return
else:
return filtered
def process_emg(args):
sig, chn_grp, chn = args
sig_path = os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn, sig)
data = np.load(sig_path)
sampling_rate = data.shape[1] // (30)
data = data.reshape(-1, 1)
# Apply bandpass filter
filtered = butter_bandpass_filter(data, EMG_LOWCUT, EMG_HIGHCUT, sampling_rate)
b_notch, a_notch = iirnotch(NOTCH_FREQ, 30, sampling_rate)
filtered = lfilter(b_notch, a_notch, filtered)
if sampling_rate != TARGET_RESAMPLE:
filtered = librosa.resample(filtered, orig_sr=sampling_rate, target_sr=TARGET_RESAMPLE, axis=0, res_type='soxr_qq')
filtered = filtered.reshape(-1, TARGET_RESAMPLE*30)
if cfg.save_type == 'npy':
# Save processed data
output_path = os.path.join(BASE_PATH, cfg.output_dir, chn_grp, chn, sig)
os.makedirs(os.path.dirname(output_path), exist_ok=True)
np.save(output_path, filtered.astype(np.float32))
return
else:
return filtered
def process_flow(args):
sig, chn_grp, chn = args
sig_path = os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn, sig)
data = np.load(sig_path)
sampling_rate = data.shape[1] // (30)
data = data.reshape(-1, 1)
# Apply bandpass filter
filtered = butter_bandpass_filter(data, FLOW_LOWCUT, FLOW_HIGHCUT, sampling_rate)
if sampling_rate != TARGET_RESAMPLE:
filtered = librosa.resample(filtered, orig_sr=sampling_rate, target_sr=TARGET_RESAMPLE, axis=0, res_type='soxr_qq')
# median filter?
filtered = filtered.reshape(-1, TARGET_RESAMPLE*30)
if cfg.save_type == 'npy':
# Save processed data
output_path = os.path.join(BASE_PATH, cfg.output_dir, chn_grp, chn, sig)
os.makedirs(os.path.dirname(output_path), exist_ok=True)
np.save(output_path, filtered.astype(np.float32))
return
else:
return filtered
def save_mmap(results, sig_list, chn_grp, chn, split='train'):
signame_list = [sig.split('.')[0] for sig in sig_list]
epoch_lengths = [sig.shape[0] for sig in results]
metadata = dict()
sig_info = dict()
start, end = 0, 0
for signame, sig in zip(signame_list, results):
length = sig.shape[0]
end = start + length
info = dict()
info['pos'] = (start, end)
info['stats'] = {'sum': float(np.sum(sig)), 'sumsq': float(np.sum(sig ** 2))}
sig_info[signame] = info
start = end
mmap_path = os.path.join(BASE_PATH, cfg.output_dir, split, chn_grp, f'{chn}.mmap')
signals_cat = np.concatenate(results, axis=0).astype(np.float32)
os.makedirs(os.path.dirname(mmap_path), exist_ok=True)
data = np.memmap(mmap_path, dtype=np.float32, mode='w+', shape=signals_cat.shape)
data[:] = signals_cat
data.flush()
metadata['sig_info'] = sig_info
metadata['data_shape'] = signals_cat.shape
info_path = os.path.join(BASE_PATH, cfg.output_dir, split, chn_grp, f'{chn}.pickle')
with open(info_path, 'wb') as f:
pickle.dump(metadata, f)
def preprocess(sig_list, chn_grp=None, chn=None, split='train'):
def _process(sig_list, chn_grp, chn, split):
print(f"Processing {chn_grp}/{chn}")
# if not (chn == "C4-A1" or chn == "AIRFLOW"): continue
if chn_grp in ['EEG','EOG']:
# sig_list = sorted(os.listdir(os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn)))
input_list = [(sig, chn_grp, chn) for sig in sig_list]
with multiprocessing.Pool(NUM_PROCESS) as pool:
results = list(tqdm(pool.imap(process_eeg, input_list), total=len(input_list)))
if cfg.save_type == 'mmap':
save_mmap(results, sig_list, chn_grp, chn, split)
elif chn_grp in ['EMG']:
# sig_list = os.listdir(os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn))
input_list = [(sig, chn_grp, chn) for sig in sig_list]
with multiprocessing.Pool(NUM_PROCESS) as pool:
results = list(tqdm(pool.imap(process_emg, input_list), total=len(input_list)))
if cfg.save_type == 'mmap':
save_mmap(results, sig_list, chn_grp, chn, split)
elif chn_grp in ['ECG']:
# sig_list = os.listdir(os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn))
input_list = [(sig, chn_grp, chn) for sig in sig_list]
with multiprocessing.Pool(NUM_PROCESS) as pool:
results = list(tqdm(pool.imap(process_ecg, input_list), total=len(input_list)))
if cfg.save_type == 'mmap':
save_mmap(results, sig_list, chn_grp, chn, split)
elif chn_grp in ['ABD', 'CHEST', 'AIRFLOW']:
# sig_list = os.listdir(os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn))
input_list = [(sig, chn_grp, chn) for sig in sig_list]
with multiprocessing.Pool(NUM_PROCESS) as pool:
results = list(tqdm(pool.imap(process_flow, input_list), total=len(input_list)))
if cfg.save_type == 'mmap':
save_mmap(results, sig_list, chn_grp, chn, split)
else:
results = []
for sig in tqdm(sig_list):
sig_path = os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn, sig)
data = np.load(sig_path)
sampling_rate = data.shape[1] // (30)
if sampling_rate != TARGET_RESAMPLE or chn == 'SaO2':
# assuming 30s epochs
data = data.reshape(-1, 1)
if chn == 'SaO2':
data = librosa.resample(data, orig_sr=sampling_rate, target_sr=1, axis=0, res_type='soxr_qq')
data = data / 1e8 # data range 0 to 1e8
if np.max(data) > 1 or np.min(data) < 0:
print(f"Warning: SaO2 values out of range: {sig} with min {np.min(data)} and max {np.max(data)}")
data = data.reshape(-1, 1*30)
else:
data = librosa.resample(data, orig_sr=sampling_rate, target_sr=TARGET_RESAMPLE, axis=0, res_type='soxr_qq')
data = data.reshape(-1, TARGET_RESAMPLE*30)
if cfg.save_type == 'npy':
# Save processed data
output_path = os.path.join(BASE_PATH, cfg.output_dir, chn_grp, chn, sig)
os.makedirs(os.path.dirname(output_path), exist_ok=True)
np.save(output_path, data)
elif cfg.save_type == 'mmap':
results.append(data)
if cfg.save_type == 'mmap':
save_mmap(results, sig_list, chn_grp, chn, split)
if chn_grp is not None and chn is not None:
_process(sig_list, chn_grp, chn, split)
return
else:
for chn_grp in os.listdir(os.path.join(BASE_PATH, cfg.data_dir)):
if not os.path.isdir(os.path.join(BASE_PATH, cfg.data_dir, chn_grp)):
continue
for chn in os.listdir(os.path.join(BASE_PATH, cfg.data_dir, chn_grp)):
if not os.path.isdir(os.path.join(BASE_PATH, cfg.data_dir, chn_grp, chn)):
continue
_process(sig_list, chn_grp, chn, split)
parser = argparse.ArgumentParser()
parser.add_argument('--data_dir', default='shhs1/signals_MAE', help='SHHS raw data location')
parser.add_argument('--output_dir', default='shhs1/mmap_signals_MAE_processed', help='SHHS processed data location')
parser.add_argument('--ann_split', action='store_true', help='To split annotation files into train/val/test')
parser.add_argument('--save_type', default='mmap', help='Which data type to save. "npy" or "mmap"')
parser.add_argument('--chn_grp', default=None, help='If specified, only preprocess this channel group')
parser.add_argument('--chn', default=None, help='If specified, only preprocess this channel')
parser.add_argument('--shhs2', action='store_true', help='SHHS2 preprocessing?')
cfg = parser.parse_args()
if __name__ == '__main__':
if not cfg.shhs2:
def get_shhs_lists(shhs_split_file):
ids = pd.read_csv(os.path.join("shhs_meta_data", shhs_split_file), header=None, names=['a'])
ids = ids['a'].values.tolist()
list_files = ["shhs1-20"+id[11:15] for id in ids]
return [id + ".npy" for id in list_files]
list_files_train = get_shhs_lists("train_list.txt")
list_files_val = get_shhs_lists("eval_list.txt")
list_files_test = get_shhs_lists("test_list.txt")
sig_list = sorted(os.listdir(os.path.join(BASE_PATH, cfg.data_dir, "EEG", "C3-A2")))
list_files_train = list(set(list_files_train).intersection(set(sig_list)))
list_files_val = list(set(list_files_val).intersection(set(sig_list)))
list_files_test = list(set(list_files_test).intersection(set(sig_list)))
print("Number of records in training set:", len(list_files_train))
print("Number of records in validation set:", len(list_files_val))
print("Number of records in test set:", len(list_files_test))
else:
# For SHHS2, use all data for preprocessing
sig_list = sorted(os.listdir(os.path.join(BASE_PATH, cfg.data_dir, "EEG", "C3-A2")))
list_files_train = sig_list
list_files_val = []
list_files_test = []
print("Processing training set...")
preprocess(list_files_train, cfg.chn_grp, cfg.chn, split='train')
print("Processing evaluation set...")
preprocess(list_files_val, cfg.chn_grp, cfg.chn, split='val')
print("Processing test set...")
preprocess(list_files_test, cfg.chn_grp, cfg.chn, split='test')
# Reorganize annotations files
if cfg.ann_split and not cfg.shhs2:
ANN_PATH = os.path.join(os.path.dirname(os.path.join(BASE_PATH, cfg.data_dir)), 'annotations')
NEW_ANN_PATH = ANN_PATH.replace('annotations', 'annotations_split')
os.makedirs(NEW_ANN_PATH, exist_ok=True)
os.makedirs(os.path.join(NEW_ANN_PATH,'train'), exist_ok=True)
os.makedirs(os.path.join(NEW_ANN_PATH,'val'), exist_ok=True)
os.makedirs(os.path.join(NEW_ANN_PATH,'test'), exist_ok=True)
for fname in tqdm(list_files_train):
ann_fname = fname.replace('.npy', '_ann.npy')
shutil.copy(os.path.join(ANN_PATH, ann_fname), os.path.join(NEW_ANN_PATH, 'train', ann_fname))
for fname in tqdm(list_files_val):
ann_fname = fname.replace('.npy', '_ann.npy')
shutil.copy(os.path.join(ANN_PATH, ann_fname), os.path.join(NEW_ANN_PATH, 'val', ann_fname))
for fname in tqdm(list_files_test):
ann_fname = fname.replace('.npy', '_ann.npy')
shutil.copy(os.path.join(ANN_PATH, ann_fname), os.path.join(NEW_ANN_PATH, 'test', ann_fname))
AH_PATH = os.path.join(BASE_PATH, 'shhs1/ah_labels')
NEW_AH_PATH = os.path.join(BASE_PATH, 'shhs1/ah_labels_split')
os.makedirs(NEW_AH_PATH, exist_ok=True)
os.makedirs(os.path.join(NEW_AH_PATH,'train'), exist_ok=True)
os.makedirs(os.path.join(NEW_AH_PATH,'val'), exist_ok=True)
os.makedirs(os.path.join(NEW_AH_PATH,'test'), exist_ok=True)
for fname in tqdm(list_files_train):
ann_fname = fname.replace('.npy', '_ah.npy')
shutil.copy(os.path.join(AH_PATH, ann_fname), os.path.join(NEW_AH_PATH, 'train', ann_fname))
for fname in tqdm(list_files_val):
ann_fname = fname.replace('.npy', '_ah.npy')
shutil.copy(os.path.join(AH_PATH, ann_fname), os.path.join(NEW_AH_PATH, 'val', ann_fname))
for fname in tqdm(list_files_test):
ann_fname = fname.replace('.npy', '_ah.npy')
shutil.copy(os.path.join(AH_PATH, ann_fname), os.path.join(NEW_AH_PATH, 'test', ann_fname))
for split in ['train', 'val', 'test']:
# create link files to respiratory channels
os.makedirs(os.path.join(BASE_PATH, cfg.output_dir, split, 'RESP'), exist_ok=True)
for chn_grp in ['ABD', 'AIRFLOW']:
chns = [f.split('.')[0] for f in os.listdir(os.path.join(BASE_PATH, cfg.output_dir, split, chn_grp))]
for chn in chns:
src_mmap = os.path.join(BASE_PATH, cfg.output_dir, split, chn_grp, f'{chn}.mmap')
src_pickle = os.path.join(BASE_PATH, cfg.output_dir, split, chn_grp, f'{chn}.pickle')
dst_mmap = os.path.join(BASE_PATH, cfg.output_dir, split, 'RESP', f'{chn}.mmap')
dst_pickle = os.path.join(BASE_PATH, cfg.output_dir, split, 'RESP', f'{chn}.pickle')
if not os.path.exists(dst_mmap):
os.symlink(src_mmap, dst_mmap)
if not os.path.exists(dst_pickle):
os.symlink(src_pickle, dst_pickle)