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import os
import glob
import pickle
import pandas as pd
import numpy as np
from tqdm import tqdm
import wfdb
import ast
from sklearn.metrics import roc_auc_score, roc_curve
from sklearn.preprocessing import StandardScaler, MultiLabelBinarizer


# EVALUATION STUFF
def generate_results(idxs, y_true, y_pred, thresholds):
    return evaluate_experiment(y_true[idxs], y_pred[idxs], thresholds)


def evaluate_experiment(y_true, y_pred, thresholds=None):
    results = {}

    if not thresholds is None:
        # binary predictions
        y_pred_binary = apply_thresholds(y_pred, thresholds)
        # PhysioNet/CinC Challenges metrics
        challenge_scores = challenge_metrics(y_true, y_pred_binary, beta1=2, beta2=2)
        results['F_beta_macro'] = challenge_scores['F_beta_macro']
        results['G_beta_macro'] = challenge_scores['G_beta_macro']
        results['TP'] = challenge_scores['TP']
        results['TN'] = challenge_scores['TN']
        results['FP'] = challenge_scores['FP']
        results['FN'] = challenge_scores['FN']
        results['Accuracy'] = challenge_scores['Accuracy']
        results['F1'] = challenge_scores['F1']
        results['Precision'] = challenge_scores['Precision']
        results['Recall'] = challenge_scores['Recall']

    # label based metric
    results['macro_auc'] = roc_auc_score(y_true, y_pred, average='macro')

    df_result = pd.DataFrame(results, index=[0])
    return df_result


def challenge_metrics(y_true, y_pred, beta1=2, beta2=2, single=False):
    f_beta = 0
    g_beta = 0
    TP, FP, TN, FN = 0., 0., 0., 0.
    Accuracy = 0
    Precision = 0
    Recall = 0
    F1 = 0

    if single:  # if evaluating single class in case of threshold-optimization
        sample_weights = np.ones(y_true.sum(axis=1).shape)
    else:
        sample_weights = y_true.sum(axis=1)
    for classi in range(y_true.shape[1]):
        y_truei, y_predi = y_true[:, classi], y_pred[:, classi]
        TP, FP, TN, FN = 0., 0., 0., 0.
        for i in range(len(y_predi)):
            sample_weight = sample_weights[i]
            if y_truei[i] == y_predi[i] == 1:
                TP += 1. / sample_weight
            if (y_predi[i] == 1) and (y_truei[i] != y_predi[i]):
                FP += 1. / sample_weight
            if y_truei[i] == y_predi[i] == 0:
                TN += 1. / sample_weight
            if (y_predi[i] == 0) and (y_truei[i] != y_predi[i]):
                FN += 1. / sample_weight
        f_beta_i = ((1 + beta1 ** 2) * TP) / ((1 + beta1 ** 2) * TP + FP + (beta1 ** 2) * FN)
        g_beta_i = TP / (TP + FP + beta2 * FN)

        f_beta += f_beta_i
        g_beta += g_beta_i

        Accuracy = (TP + TN) / (FP + TP + TN + FN)
        # Precision = TP / (TP + FP)
        # Recall = TP / (TP + FN)
        # F1 =  2*(Precision * Recall) / (Precision + Recall)
        F1 = 2 * TP / 2 * TP + FP + FN

    return {'F_beta_macro': f_beta / y_true.shape[1], 'G_beta_macro': g_beta / y_true.shape[1], 'TP': TP, 'FP': FP,
            'TN': TN, 'FN': FN, 'Accuracy': Accuracy, 'F1': F1, 'Precision': Precision, 'Recall': Recall}


def get_appropriate_bootstrap_samples(y_true, n_bootstraping_samples):
    samples = []
    while True:
        ridxs = np.random.randint(0, len(y_true), len(y_true))
        if y_true[ridxs].sum(axis=0).min() != 0:
            samples.append(ridxs)
            if len(samples) == n_bootstraping_samples:
                break
    return samples


def find_optimal_cutoff_threshold(target, predicted):
    """
    Find the optimal probability cutoff point for a classification model related to event rate
    """
    fpr, tpr, threshold = roc_curve(target, predicted)
    optimal_idx = np.argmax(tpr - fpr)
    optimal_threshold = threshold[optimal_idx]
    return optimal_threshold


def find_optimal_cutoff_thresholds(y_true, y_pred):
    return [find_optimal_cutoff_threshold(y_true[:, i], y_pred[:, i]) for i in range(y_true.shape[1])]


def find_optimal_cutoff_threshold_for_Gbeta(target, predicted, n_thresholds=100):
    thresholds = np.linspace(0.00, 1, n_thresholds)
    scores = [challenge_metrics(target, predicted > t, single=True)['G_beta_macro'] for t in thresholds]
    optimal_idx = np.argmax(scores)
    return thresholds[optimal_idx]


def find_optimal_cutoff_thresholds_for_Gbeta(y_true, y_pred):
    print("optimize thresholds with respect to G_beta")
    return [
        find_optimal_cutoff_threshold_for_Gbeta(y_true[:, k][:, np.newaxis], y_pred[:, k][:, np.newaxis])
        for k in tqdm(range(y_true.shape[1]))]


def apply_thresholds(preds, thresholds):
    """
        apply class-wise thresholds to prediction score in order to get binary format.
        BUT: if no score is above threshold, pick maximum. This is needed due to metric issues.
    """
    tmp = []
    for p in preds:
        tmp_p = (p > thresholds).astype(int)
        if np.sum(tmp_p) == 0:
            tmp_p[np.argmax(p)] = 1
        tmp.append(tmp_p)
    tmp = np.array(tmp)
    return tmp


# DATA PROCESSING STUFF
def load_dataset(path, sampling_rate, release=False):
    if path.split('/')[-2] == 'ptbxl':
        # load and convert annotation data
        Y = pd.read_csv(path + 'ptbxl_database.csv', index_col='ecg_id')
        Y.scp_codes = Y.scp_codes.apply(lambda x: ast.literal_eval(x))

        # Load raw signal data
        X = load_raw_data_ptbxl(Y, sampling_rate, path)

    elif path.split('/')[-2] == 'ICBEB':
        # load and convert annotation data
        Y = pd.read_csv(path + 'icbeb_database.csv', index_col='ecg_id')
        Y.scp_codes = Y.scp_codes.apply(lambda x: ast.literal_eval(x))

        # Load raw signal data
        X = load_raw_data_icbeb(Y, sampling_rate, path)

    return X, Y


def load_raw_data_icbeb(df, sampling_rate, path):
    if sampling_rate == 100:
        if os.path.exists(path + 'raw100.npy'):
            data = np.load(path + 'raw100.npy', allow_pickle=True)
        else:
            data = [wfdb.rdsamp(path + 'records100/' + str(f)) for f in tqdm(df.index)]
            data = np.array([signal for signal, meta in data])
            pickle.dump(data, open(path + 'raw100.npy', 'wb'), protocol=4)
    elif sampling_rate == 500:
        if os.path.exists(path + 'raw500.npy'):
            data = np.load(path + 'raw500.npy', allow_pickle=True)
        else:
            data = [wfdb.rdsamp(path + 'records500/' + str(f)) for f in tqdm(df.index)]
            data = np.array([signal for signal, meta in data])
            pickle.dump(data, open(path + 'raw500.npy', 'wb'), protocol=4)
    return data


def load_raw_data_ptbxl(df, sampling_rate, path):
    if sampling_rate == 100:
        if os.path.exists(path + 'raw100.npy'):
            data = np.load(path + 'raw100.npy', allow_pickle=True)
        else:
            data = [wfdb.rdsamp(path + f) for f in tqdm(df.filename_lr)]
            data = np.array([signal for signal, meta in data])
            pickle.dump(data, open(path + 'raw100.npy', 'wb'), protocol=4)
    elif sampling_rate == 500:
        if os.path.exists(path + 'raw500.npy'):
            data = np.load(path + 'raw500.npy', allow_pickle=True)
        else:
            data = [wfdb.rdsamp(path + f) for f in tqdm(df.filename_hr)]
            data = np.array([signal for signal, meta in data])
            pickle.dump(data, open(path + 'raw500.npy', 'wb'), protocol=4)
    return data


def compute_label_aggregations(df, folder, ctype):
    df['scp_codes_len'] = df.scp_codes.apply(lambda x: len(x))

    aggregation_df = pd.read_csv(folder + 'scp_statements.csv', index_col=0)

    if ctype in ['diagnostic', 'subdiagnostic', 'superdiagnostic']:

        def aggregate_all_diagnostic(y_dic):
            tmp = []
            for key in y_dic.keys():
                if key in diag_agg_df.index:
                    tmp.append(key)
            return list(set(tmp))

        def aggregate_subdiagnostic(y_dic):
            tmp = []
            for key in y_dic.keys():
                if key in diag_agg_df.index:
                    c = diag_agg_df.loc[key].diagnostic_subclass
                    if str(c) != 'nan':
                        tmp.append(c)
            return list(set(tmp))

        def aggregate_diagnostic(y_dic):
            tmp = []
            for key in y_dic.keys():
                if key in diag_agg_df.index:
                    c = diag_agg_df.loc[key].diagnostic_class
                    if str(c) != 'nan':
                        tmp.append(c)
            return list(set(tmp))

        diag_agg_df = aggregation_df[aggregation_df.diagnostic == 1.0]
        if ctype == 'diagnostic':
            df['diagnostic'] = df.scp_codes.apply(aggregate_all_diagnostic)
            df['diagnostic_len'] = df.diagnostic.apply(lambda x: len(x))
        elif ctype == 'subdiagnostic':
            df['subdiagnostic'] = df.scp_codes.apply(aggregate_subdiagnostic)
            df['subdiagnostic_len'] = df.subdiagnostic.apply(lambda x: len(x))
        elif ctype == 'superdiagnostic':
            df['superdiagnostic'] = df.scp_codes.apply(aggregate_diagnostic)
            df['superdiagnostic_len'] = df.superdiagnostic.apply(lambda x: len(x))
    elif ctype == 'form':
        form_agg_df = aggregation_df[aggregation_df.form == 1.0]

        def aggregate_form(y_dic):
            tmp = []
            for key in y_dic.keys():
                if key in form_agg_df.index:
                    c = key
                    if str(c) != 'nan':
                        tmp.append(c)
            return list(set(tmp))

        df['form'] = df.scp_codes.apply(aggregate_form)
        df['form_len'] = df.form.apply(lambda x: len(x))
    elif ctype == 'rhythm':
        rhythm_agg_df = aggregation_df[aggregation_df.rhythm == 1.0]

        def aggregate_rhythm(y_dic):
            tmp = []
            for key in y_dic.keys():
                if key in rhythm_agg_df.index:
                    c = key
                    if str(c) != 'nan':
                        tmp.append(c)
            return list(set(tmp))

        df['rhythm'] = df.scp_codes.apply(aggregate_rhythm)
        df['rhythm_len'] = df.rhythm.apply(lambda x: len(x))
    elif ctype == 'all':
        df['all_scp'] = df.scp_codes.apply(lambda x: list(set(x.keys())))

    return df


def select_data(XX, YY, ctype, min_samples, output_folder):
    # convert multi_label to multi-hot
    mlb = MultiLabelBinarizer()

    if ctype == 'diagnostic':
        X = XX[YY.diagnostic_len > 0]
        Y = YY[YY.diagnostic_len > 0]
        mlb.fit(Y.diagnostic.values)
        y = mlb.transform(Y.diagnostic.values)
    elif ctype == 'subdiagnostic':
        counts = pd.Series(np.concatenate(YY.subdiagnostic.values)).value_counts()
        counts = counts[counts > min_samples]
        YY.subdiagnostic = YY.subdiagnostic.apply(lambda x: list(set(x).intersection(set(counts.index.values))))
        YY['subdiagnostic_len'] = YY.subdiagnostic.apply(lambda x: len(x))
        X = XX[YY.subdiagnostic_len > 0]
        Y = YY[YY.subdiagnostic_len > 0]
        mlb.fit(Y.subdiagnostic.values)
        y = mlb.transform(Y.subdiagnostic.values)
    elif ctype == 'superdiagnostic':
        counts = pd.Series(np.concatenate(YY.superdiagnostic.values)).value_counts()
        counts = counts[counts > min_samples]
        YY.superdiagnostic = YY.superdiagnostic.apply(lambda x: list(set(x).intersection(set(counts.index.values))))
        YY['superdiagnostic_len'] = YY.superdiagnostic.apply(lambda x: len(x))
        X = XX[YY.superdiagnostic_len > 0]
        Y = YY[YY.superdiagnostic_len > 0]
        mlb.fit(Y.superdiagnostic.values)
        y = mlb.transform(Y.superdiagnostic.values)
    elif ctype == 'form':
        # filter
        counts = pd.Series(np.concatenate(YY.form.values)).value_counts()
        counts = counts[counts > min_samples]
        YY.form = YY.form.apply(lambda x: list(set(x).intersection(set(counts.index.values))))
        YY['form_len'] = YY.form.apply(lambda x: len(x))
        # select
        X = XX[YY.form_len > 0]
        Y = YY[YY.form_len > 0]
        mlb.fit(Y.form.values)
        y = mlb.transform(Y.form.values)
    elif ctype == 'rhythm':
        # filter
        counts = pd.Series(np.concatenate(YY.rhythm.values)).value_counts()
        counts = counts[counts > min_samples]
        YY.rhythm = YY.rhythm.apply(lambda x: list(set(x).intersection(set(counts.index.values))))
        YY['rhythm_len'] = YY.rhythm.apply(lambda x: len(x))
        # select
        X = XX[YY.rhythm_len > 0]
        Y = YY[YY.rhythm_len > 0]
        mlb.fit(Y.rhythm.values)
        y = mlb.transform(Y.rhythm.values)
    elif ctype == 'all':
        # filter
        counts = pd.Series(np.concatenate(YY.all_scp.values)).value_counts()
        counts = counts[counts > min_samples]
        YY.all_scp = YY.all_scp.apply(lambda x: list(set(x).intersection(set(counts.index.values))))
        YY['all_scp_len'] = YY.all_scp.apply(lambda x: len(x))
        # select
        X = XX[YY.all_scp_len > 0]
        Y = YY[YY.all_scp_len > 0]
        mlb.fit(Y.all_scp.values)
        y = mlb.transform(Y.all_scp.values)
    else:
        pass

    # save Label_Binarizer
    with open(output_folder + 'mlb.pkl', 'wb') as tokenizer:
        pickle.dump(mlb, tokenizer)

    return X, Y, y, mlb


def preprocess_signals(X_train, X_validation, X_test, outputfolder):
    # Standardize data such that mean 0 and variance 1
    ss = StandardScaler()
    ss.fit(np.vstack(X_train).flatten()[:, np.newaxis].astype(float))

    # Save Standardize data
    with open(outputfolder + 'standard_scaler.pkl', 'wb') as ss_file:
        pickle.dump(ss, ss_file)

    return apply_standardizer(X_train, ss), apply_standardizer(X_validation,
                                                               ss), apply_standardizer(
        X_test, ss)


def apply_standardizer(X, ss):
    X_tmp = []
    for x in X:
        x_shape = x.shape
        X_tmp.append(ss.transform(x.flatten()[:, np.newaxis]).reshape(x_shape))
    X_tmp = np.array(X_tmp)
    return X_tmp


# DOCUMENTATION STUFF

def generate_ptbxl_summary_table(selection=None, folder='/output/'):
    exps = ['exp0', 'exp1', 'exp1.1', 'exp1.1.1', 'exp2', 'exp3']
    metrics = ['macro_auc', 'Accuracy', 'TP', 'TN', 'FP', 'FN', 'Precision', 'Recall', 'F1']
    #     0            1        2     3     4    5        6          7        8

    # get models
    models = {}
    for i, exp in enumerate(exps):
        if selection is None:
            exp_models = [m.split('/')[-1] for m in glob.glob(folder + str(exp) + '/models/*')]
        else:
            exp_models = selection
        if i == 0:
            models = set(exp_models)
        else:
            models = models.union(set(exp_models))

    results_dic = {'Method': [],
                   'exp0_macro_auc': [],
                   'exp1_macro_auc': [],
                   'exp1.1_macro_auc': [],
                   'exp1.1.1_macro_auc': [],
                   'exp2_macro_auc': [],
                   'exp3_macro_auc': [],
                   'exp0_Accuracy': [],
                   'exp1_Accuracy': [],
                   'exp1.1_Accuracy': [],
                   'exp1.1.1_Accuracy': [],
                   'exp2_Accuracy': [],
                   'exp3_Accuracy': [],
                   'exp0_F1': [],
                   'exp1_F1': [],
                   'exp1.1_F1': [],
                   'exp1.1.1_F1': [],
                   'exp2_F1': [],
                   'exp3_F1': [],
                   'exp0_Precision': [],
                   'exp1_Precision': [],
                   'exp1.1_Precision': [],
                   'exp1.1.1_Precision': [],
                   'exp2_Precision': [],
                   'exp3_Precision': [],
                   'exp0_Recall': [],
                   'exp1_Recall': [],
                   'exp1.1_Recall': [],
                   'exp1.1.1_Recall': [],
                   'exp2_Recall': [],
                   'exp3_Recall': [],
                   'exp0_TP': [],
                   'exp1_TP': [],
                   'exp1.1_TP': [],
                   'exp1.1.1_TP': [],
                   'exp2_TP': [],
                   'exp3_TP': [],
                   'exp0_TN': [],
                   'exp1_TN': [],
                   'exp1.1_TN': [],
                   'exp1.1.1_TN': [],
                   'exp2_TN': [],
                   'exp3_TN': [],
                   'exp0_FP': [],
                   'exp1_FP': [],
                   'exp1.1_FP': [],
                   'exp1.1.1_FP': [],
                   'exp2_FP': [],
                   'exp3_FP': [],
                   'exp0_FN': [],
                   'exp1_FN': [],
                   'exp1.1_FN': [],
                   'exp1.1.1_FN': [],
                   'exp2_FN': [],
                   'exp3_FN': []
                   }

    for m in models:
        results_dic['Method'].append(m)

        for e in exps:

            try:
                me_res = pd.read_csv(folder + str(e) + '/models/' + str(m) + '/results/te_results.csv', index_col=0)

                mean1 = me_res.loc['point'][metrics[0]]
                unc1 = max(me_res.loc['upper'][metrics[0]] - me_res.loc['point'][metrics[0]],
                           me_res.loc['point'][metrics[0]] - me_res.loc['lower'][metrics[0]])

                acc = me_res.loc['point'][metrics[1]]
                f1 = me_res.loc['point'][metrics[8]]
                precision = me_res.loc['point'][metrics[6]]
                recall = me_res.loc['point'][metrics[7]]
                tp = me_res.loc['point'][metrics[2]]
                tn = me_res.loc['point'][metrics[3]]
                fp = me_res.loc['point'][metrics[4]]
                fn = me_res.loc['point'][metrics[5]]

                results_dic[e + '_macro_auc'].append("%.3f(%.2d)" % (np.round(mean1, 3), int(unc1 * 1000)))
                results_dic[e + '_Accuracy'].append("%.3f" % acc)
                results_dic[e + '_F1'].append("%.3f" % f1)
                results_dic[e + '_Precision'].append("%.3f" % precision)
                results_dic[e + '_Recall'].append("%.3f" % recall)
                results_dic[e + '_TP'].append("%.3f" % tp)
                results_dic[e + '_TN'].append("%.3f" % tn)
                results_dic[e + '_FP'].append("%.3f" % fp)
                results_dic[e + '_FN'].append("%.3f" % fn)

            except FileNotFoundError:
                results_dic[e + '_macro_auc'].append("--")
                results_dic[e + '_Accuracy'].append("--")
                results_dic[e + '_F1'].append("--")
                results_dic[e + '_Precision'].append("--")
                results_dic[e + '_Recall'].append("--")
                results_dic[e + '_TP'].append("--")
                results_dic[e + '_TN'].append("--")
                results_dic[e + '_FP'].append("--")
                results_dic[e + '_FN'].append("--")

    df = pd.DataFrame(results_dic)
    df_index = df[df.Method.isin(['naive', 'ensemble'])]
    df_rest = df[~df.Method.isin(['naive', 'ensemble'])]
    df = pd.concat([df_rest, df_index])
    df.to_csv(folder + 'results_ptbxl.csv')

    titles = [
        '### 1. PTB-XL: all statements',
        '### 2. PTB-XL: diagnostic statements',
        '### 3. PTB-XL: Diagnostic subclasses',
        '### 4. PTB-XL: Diagnostic superclasses',
        '### 5. PTB-XL: Form statements',
        '### 6. PTB-XL: Rhythm statements'
    ]

    # helper output function for markdown tables
    our_work = 'https://arxiv.org/abs/2004.13701'
    our_repo = 'https://github.com/helme/ecg_ptbxl_benchmarking/'
    md_source = ''
    for i, e in enumerate(exps):
        md_source += '\n ' + titles[i] + ' \n \n'
        md_source += '|    Model    |    AUC    |\n'

        for row in df_rest[['Method', e + '_AUC']].sort_values(e + '_AUC', ascending=False).values:
            md_source += '| ' + row[0].replace('fastai_', '') + ' | ' + row[1] + ' |\n'
    print(md_source)