Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology.
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- [1] § Materials and methods › Construction and validation of diagnostic cytology model for BM metastasis in neuroblastoma ↔ feature_extraction/deep_learning_training/Model building and evaluation.ipynb, lines 286–325 · score 0.50 · NPV, PPV, thresholds, sensitivity, metric, WSI
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The authors' code
Jupyter notebook · 464 lines · 15 KB · no license · 1 match
- # %% [markdown]
- # %%
- # Model building and evaluation
- 1. data verification and review
- 2. data regularization which changes the data to obey N~(0, 1)
- 3. construct the training and test sets
- 4. features screening through Lasso and select non-zero items for the subsequent model
- 5. Use machine learning algorithms for clinical task
- 6. Model visualization
- # feature_file: the path of the feature data
- # label_file: label information file for each sample
- # labels: targets to be learned by the AI system
- import os
- from IPython.display import display
- os.environ['KMP_DUPLICATE_LIB_OK'] = 'TRUE'
- from onekey_algo import OnekeyDS as okds
- import pandas as pd
- os.makedirs('img', exist_ok=True)
- os.makedirs('results', exist_ok=True)
- os.makedirs('features', exist_ok=True)
- # file settings
- label_file = r'label information file for each sample'
- feature_file = r'the path of your feature data'
- labels = ['label']
- # %% [markdown]
- # %%
- # read the column name of labeled file
- # read data, the data is stored in CSV forma
- # the required label_data is a 'DataFrame' format including the ID column and the subsequent labels column which can be multiple columns
- feature_data = pd.read_csv(feature_file)
- display(feature_data)
- label_data = pd.read_csv(label_file)
- label_data.head()
- # %% [markdown]
- # %%
- # feature splicing
- from onekey_algo.custom.utils import print_join_info
- print_join_info(feature_data, label_data)
- combined_data = pd.merge(feature_data, label_data, on=['ID'], how='inner')
- ids = combined_data['ID']
- combined_data = combined_data.drop(['ID'], axis=1)
- print(combined_data[labels].value_counts())
- combined_data.columns
- # %% [markdown]
- # %%
- combined_data.describe()
- # %% [markdown]
- # #normalize_df,change the data to a mean of 0,a variance of 1
- #
- # $column = \frac{column - mean}{std}$
- # %%
- # regularization
- from onekey_algo.custom.components.comp1 import normalize_df
- data = normalize_df(combined_data, not_norm=labels, group='group')
- data = data.dropna(axis=1)
- data.describe()
- # %% [markdown]
- # %%
- # correlation coefficient,there are three methods to choose from for calculating the correlation coefficient
- 1. pearson: standard correlation coefficient
- 2. kendall: Kendall Tau correlation coefficient
- 3. spearman: Spearman rank correlation
- pearson_corr = data[data['group'] == 'train'][[c for c in data.columns if c not in labels]].corr('pearson')
- # kendall_corr = data[[c for c in data.columns if c not in labels]].corr('kendall')
- # spearman_corr = data[[c for c in data.columns if c not in labels]].corr('spearman')
- # %% [markdown]
- # %%
- # visualization of correlation coefficient
- import seaborn as sns
- import matplotlib.pyplot as plt
- from onekey_algo.custom.components.comp1 import draw_matrix
- if combined_data.shape[1] < 100:
- plt.figure(figsize=(50.0, 40.0))
- # select the correlation coefficient for visualization
- draw_matrix(pearson_corr, annot=True, cmap='YlGnBu', cbar=False)
- plt.savefig(f'img/feature_corr.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # cluster analysis
- import seaborn as sns
- import matplotlib.pyplot as plt
- if combined_data.shape[1] < 100:
- pp = sns.clustermap(pearson_corr, linewidths=.5, figsize=(50.0, 40.0), cmap='YlGnBu')
- plt.setp(pp.ax_heatmap.get_yticklabels(), rotation=0)
- plt.savefig(f'img/feature_cluster.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # feature filtering--correlation coefficient
- def select_feature(corr threshold: float = 0.9 keep: int = 1 topn=10 verbose=False):
- from onekey_algo.custom.components.comp1
- import select_feature
- sel_feature = select_feature(pearson_corr, threshold=0.9, topn=32, verbose=False)
- sel_feature = sel_feature + labels + ['group']
- sel_feature
- # %% [markdown]
- # %%
- # features screening
- sel_data = data[sel_feature]
- sel_data.describe()
- # %%
- # %%
- # construct datasets
- import numpy as np
- import onekey_algo.custom.components as okcomp
- n_classes = 2
- train_data = sel_data[(sel_data['group'] == 'train')]
- train_ids = ids[train_data.index]
- train_data = train_data.reset_index()
- train_data = train_data.drop('index', axis=1)
- y_data = train_data[labels]
- X_data = train_data.drop(labels + ['group'], axis=1)
- test_data = sel_data[sel_data['group'] != 'train']
- test_ids = ids[test_data.index]
- test_data = test_data.reset_index()
- test_data = test_data.drop('index', axis=1)
- y_test_data = test_data[labels]
- X_test_data = test_data.drop(labels + ['group'], axis=1)
- y_all_data = sel_data[labels]
- X_all_data = sel_data.drop(labels + ['group'], axis=1)
- column_names = X_data.columns
- print(f"sample size in the training set:{X_data.shape}, sample size in the validation set:{X_test_data.shape}")
- # %% [markdown]
- # %%
- # Lasso, initialize the Lasso model with alpha as the penalty coefficient
- # reference (https://scikit-learn.org/stable/modules/generated/sklearn.linear_model.Lasso.html?highlight=lasso#sklearn.linear_model.Lasso)
- alpha = okcomp.comp1.lasso_cv_coefs(X_data, y_data, column_names=None, alpha_logmin=-3)
- plt.savefig(f'img/feature_lasso.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- okcomp.comp1.lasso_cv_efficiency(X_data, y_data, points=50, alpha_logmin=-3)
- plt.savefig(f'img/feature_mse_label.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # penalty factor, use the penalty factor of cross-validation as the basis for model training
- from sklearn import linear_model
- models = []
- for label in labels:
- clf = linear_model.Lasso(alpha=alpha)
- clf.fit(X_data, y_data[label])
- models.append(clf)
- # %% [markdown]
- # %%
- # feature screening, screened features with coef > 0 and print
- COEF_THRESHOLD = 1e-8 # feature thresholds after filtering
- scores = []
- selected_features = []
- for label, model in zip(labels, models):
- feat_coef = [(feat_name, coef) for feat_name, coef in zip(column_names, model.coef_)
- if COEF_THRESHOLD is None or abs(coef) > COEF_THRESHOLD]
- selected_features.append([feat for feat, _ in feat_coef])
- formula = ' '.join([f"{coef:+.6f} * {feat_name}" for feat_name, coef in feat_coef])
- score = f"{label} = {model.intercept_} {'+' if formula[0] != '-' else ''} {formula}"
- scores.append(score)
- print(scores[0])
- # %% [markdown]
- # %%
- # feature weights
- feat_coef = sorted(feat_coef, key=lambda x: x[1])
- feat_coef_df = pd.DataFrame(feat_coef, columns=['feature_name', 'Coefficients'])
- feat_coef_df.plot(x='feature_name', y='Coefficients', kind='barh')
- plt.savefig(f'img/feature_weights.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # screening features, use the features with high coefficients screened by Lasso as training data
- X_data = X_data[selected_features[0]]
- X_test_data = X_test_data[selected_features[0]]
- X_data.columns
- # %% [markdown]
- # %%
- # model selection
- model_names = ['ExtraTrees','RandomForest','LightGBM','AdaBoost', 'LR', 'MLP']
- models = okcomp.comp1.create_clf_model(model_names)
- model_names = list(models.keys())
- # %% [markdown]
- # %%
- # cross validation (if the study needed, no need in multicenterc ohort)
- # import seaborn as sns
- # import matplotlib.pyplot as plt
- # import pandas as pd
- # from sklearn.metrics import accuracy_score, roc_auc_score
- # results = okcomp.comp1.get_bst_split(X_data, y_data, models, test_size=0.2, metric_fn=roc_auc_score, cv=True, random_state=0)
- _, (X_train_sel, X_test_sel, y_train_sel, y_test_sel) = results['results'][results['max_idx']]
- # X_train_sel, X_test_sel, y_train_sel, y_test_sel = X_data, X_test_data, y_data, y_test_data
- # trails, _ = zip(*results['results'])
- # cv_results = pd.DataFrame(trails, columns=model_names)
- # sns.boxplot(data=cv_results)
- # plt.ylabel('AUC %')
- # plt.xlabel('Model Nmae')
- # plt.savefig(f'img/model_cv.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # model selection and evaluation
- import joblib
- from onekey_algo.custom.components.comp1 import plot_feature_importance, plot_learning_curve, smote_resample
- targets = []
- os.makedirs('models', exist_ok=True)
- for l in labels:
- new_models = list(okcomp.comp1.create_clf_model(model_names).values())
- for mn, m in zip(model_names, new_models):
- X_train_smote, y_train_smote = X_train_sel, y_train_sel
- # X_train_smote, y_train_smote = smote_resample(X_train_sel, y_train_sel)
- m.fit(X_train_smote, y_train_smote[l])
- # save result
- joblib.dump(m, f'models/{mn}_{l}.pkl')
- plot_feature_importance(m, selected_features[0], save_dir='img')
- # plot_learning_curve(m, X_train_sel, y_train_sel, title=f'Learning Curve {mn}')
- # plt.savefig(f"img/Rad_{mn}_learning_curve.svg", bbox_inches='tight')
- plt.show()
- targets.append(new_models)
- # %% [markdown]
- # %%
- # WSI-level predictions
- # predictions for prediction results of each model corresponding to each label.
- # pred_scores for predicted probability value for each model for each label.
- from sklearn.metrics import accuracy_score
- from sklearn.preprocessing import OneHotEncoder
- from onekey_algo.custom.components.delong import calc_95_CI
- from onekey_algo.custom.components.metrics import analysis_pred_binary
- predictions = [[(model.predict(X_train_sel), model.predict(X_test_sel))
- for model in target] for label, target in zip(labels, targets)]
- pred_scores = [[(model.predict_proba(X_train_sel), model.predict_proba(X_test_sel))
- for model in target] for label, target in zip(labels, targets)]
- metric = []
- pred_sel_idx = []
- for label, prediction, scores in zip(labels, predictions, pred_scores):
- pred_sel_idx_label = []
- for mname, (train_pred, test_pred), (train_score, test_score) in zip(model_names, prediction, scores):
- acc, auc, ci, tpr, tnr, ppv, npv, precision, recall, f1, thres = analysis_pred_binary(y_train_sel[label],
- train_score[:, 1])
- ci = f"{ci[0]:.4f} - {ci[1]:.4f}"
- metric.append((mname, acc, auc, ci, tpr, tnr, ppv, npv, precision, recall, f1, thres, f"{label}-train"))
- acc, auc, ci, tpr, tnr, ppv, npv, precision, recall, f1, thres = analysis_pred_binary(y_test_sel[label],
- test_score[:, 1])
- ci = f"{ci[0]:.4f} - {ci[1]:.4f}"
- metric.append((mname, acc, auc, ci, tpr, tnr, ppv, npv, precision, recall, f1, thres, f"{label}-test"))
- pred_sel_idx_label.append(np.logical_or(test_score[:, 0] >= thres, test_score[:, 1] >= thres))
- pred_sel_idx.append(pred_sel_idx_label)
- metric = pd.DataFrame(metric, index=None, columns=['model_name', 'Accuracy', 'AUC', '95% CI',
- 'Sensitivity', 'Specificity',
- 'PPV', 'NPV', 'Precision', 'Recall', 'F1',
- 'Threshold', 'Task'])
- metric
- # %% [markdown]
- # %%
- # draw curves
- import seaborn as sns
- plt.figure(figsize=(10, 10))
- plt.subplot(211)
- sns.barplot(x='model_name', y='Accuracy', data=metric, hue='Task')
- plt.subplot(212)
- sns.lineplot(x='model_name', y='Accuracy', data=metric, hue='Task')
- plt.savefig(f'img/model_acc.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # ROC
- sel_model = model_names
- for sm in sel_model:
- if sm in model_names:
- sel_model_idx = model_names.index(sm)
- # Plot all ROC curves
- plt.figure(figsize=(8, 8))
- for pred_score, label in zip(pred_scores, labels):
- okcomp.comp1.draw_roc([np.array(y_train_sel[label]), np.array(y_test_sel[label])],
- pred_score[sel_model_idx],
- labels=['Train', 'Test'], title=f"Model: {sm}")
- plt.savefig(f'img/model_{sm}_roc.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # model result
- sel_model = model_names
- for pred_score, label in zip(pred_scores, labels):
- pred_test_scores = []
- for sm in sel_model:
- if sm in model_names:
- sel_model_idx = model_names.index(sm)
- pred_test_scores.append(pred_score[sel_model_idx][1])
- okcomp.comp1.draw_roc([np.array(y_test_sel[label])] * len(pred_test_scores),
- pred_test_scores,
- labels=sel_model, title=f"Model AUC")
- plt.savefig(f'img/model_roc.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # DCA
- from onekey_algo.custom.components.comp1 import plot_DCA
- for pred_score, label in zip(pred_scores, labels):
- pred_test_scores = []
- for sm in sel_model:
- if sm in model_names:
- sel_model_idx = model_names.index(sm)
- okcomp.comp1.plot_DCA(pred_score[sel_model_idx][1][:,1], np.array(y_test_sel[label]),
- title=f'Rad Model {sm} DCA')
- plt.savefig(f'img/model_{sm}_dca.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # confusion matrix
- # set the drawing parameters
- sel_model = model_names
- c_matrix = {}
- for sm in sel_model:
- if sm in model_names:
- sel_model_idx = model_names.index(sm)
- for idx, label in enumerate(labels):
- cm = okcomp.comp1.calc_confusion_matrix(predictions[idx][sel_model_idx][-1], y_test_sel[label],
- # sel_idx = pred_sel_idx[idx][sel_model_idx],
- class_mapping={1:'1', 0:'0'}, num_classes=2)
- c_matrix[label] = cm
- plt.figure(figsize=(5, 4))
- plt.title(f'Rad Model:{sm}')
- okcomp.comp1.draw_matrix(cm, norm=False, annot=True, cmap='Blues', fmt='.3g')
- plt.savefig(f'img/model_{sm}_cm.svg', bbox_inches = 'tight')
- # %% [markdown]
- # %%
- # sample prediction histogram
- # plot the predicted results and the corresponding true results for each sample
- sel_model = model_names
- c_matrix = {}
- for sm in sel_model:
- if sm in model_names:
- sel_model_idx = model_names.index(sm)
- for idx, label in enumerate(labels):
- okcomp.comp1.draw_predict_score(pred_scores[idx][sel_model_idx][-1], y_test_sel[label])
- plt.title(f'{sm} sample predict score')
- plt.legend(labels=["label=0","label=1"],loc="lower right")
- plt.savefig(f'img/model_{sm}_sample_dis.svg', bbox_inches = 'tight')
- plt.show()
- # %% [markdown]
- # %% [markdown]
- # #save model result
- # import os
- # import numpy as np
- #
- # os.makedirs('results', exist_ok=True)
- # sel_model = sel_model
- #
- # for idx, label in enumerate(labels):
- # for sm in sel_model:
- # if sm in model_names:
- # sel_model_idx = model_names.index(sm)
- # target = targets[idx][sel_model_idx]
- # # sample prediction result
- # train_indexes = np.reshape(np.array(train_ids), (-1, 1)).astype(str)
- # test_indexes = np.reshape(np.array(test_ids), (-1, 1)).astype(str)
- # y_train_pred_scores = target.predict_proba(X_train_sel)
- # y_test_pred_scores = target.predict_proba(X_test_sel)
- # columns = ['ID'] + [f"{label}-{i}"for i in range(y_test_pred_scores.shape[1])]
- # # save results
- # result_train = pd.DataFrame(np.concatenate([train_indexes, y_train_pred_scores], axis=1), columns=columns)
- # result_train.to_csv(f'results/{sm}_Rad_train.csv', index=False)
- # result_test = pd.DataFrame(np.concatenate([test_indexes, y_test_pred_scores], axis=1), columns=columns)
- # result_test.to_csv(f'results/{sm}_Rad_test.csv', index=False)
- # %%
Model building and evaluation.ipynb at commit d1a39a2, no license · at the source
Overview
13 affiliations
- Department of Laboratory Medicine, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092 China
- Faculty of Medical Laboratory Science, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025 China
- Institute of Artificial Intelligence Medicine, Shanghai Academy of Experimental Medicine, Shanghai, 200092 China
- Department of Laboratory Medicine, Shenzhen Children’s Hospital, Affiliated to Shantou University Medical College, Shenzhen, 518038 China
- National Clinical Trial Institute, Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Children and Adolescents’ Health and Diseases, Hangzhou, Zhejiang 310052 China
- Research Center for Clinical Pharmacy, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, Zhejiang 310058 China
- School of Communication and Information Engineering, Shanghai University, Shanghai, 200444 China
- Department of Pediatric Hematology/Oncology, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092 China
- Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092 China
- Shanghai Engineering Research Center of Intelligence Pediatrics (SERCIP), Shanghai, 200127 China
- Pediatric Cancer Research Center, Zhejiang University School of Medicine, National Clinical Research Center for Children and Adolescents’ Health and Diseases, Hangzhou, Zhejiang 310052 China
- Department of Surgical Oncology, Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Children and Adolescents’ Health and Diseases, Hangzhou, Zhejiang 310052 China
- Department of Clinical Laboratory, Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Children and Adolescents’ Health and Diseases, Hangzhou, Zhejiang 310052 China
Abstract
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Repository
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dr-jenna/cMIL
d1a39a23789e2f53cefcf05af2dc6b2fa59b42e1, 16 January 2025Availability: 1 check, the latest on 29 September 2026: the link answers
- 29 September 2026: the link answers
33 files
- feature_extraction/
deep_learning_training/ , Jupyter, 45 linesDataset splitting.ipynb - feature_extraction/
deep_learning_training/ , Jupyter, 464 lines, 1 matchModel building and evaluation.ipynb - feature_extraction/
deep_learning_training/ , Python, 362 linesModel building and evaluation.py - feature_extraction/
deep_learning_training/ , Jupyter, 47 linesMulti Instance Learning.ipynb - feature_extraction/
deep_learning_training/ , Python, 49 linesMulti Instance Learning.py - feature_extraction/
deep_learning_training/ , Jupyter, 83 linesPatch feature extraction.ipynb - feature_extraction/
deep_learning_training/ , Python, 50 linesPatch feature extraction.py - feature_extraction/
deep_learning_training/ , Jupyter, 45 linesPatch level prediction/ Dataset splitting.ipynb - feature_extraction/
deep_learning_training/ , Jupyter, 120 linesPatch level prediction/ What-feature.ipynb - feature_extraction/
onekey_core/ , Python, 30 lines__init__.py - feature_extraction/
onekey_core/ , Python, 13 linescore/ __init__.py - feature_extraction/
onekey_core/ , Python, 40 linescore/ image_loader.py - feature_extraction/
onekey_core/ , Python, 68 linescore/ losses_factory.py - feature_extraction/
onekey_core/ , Python, 35 linescore/ model_factory.py - feature_extraction/
onekey_core/ , Python, 59 linescore/ optimizer_lr_factory.py - feature_extraction/
onekey_core/ , Python, 58 linescore/ test_factory.py - feature_extraction/
onekey_core/ , Python, 31 linesextension.py - feature_extraction/
onekey_core/ , Python, 12 linesmodels/ __init__.py - feature_extraction/
onekey_core/ , Python, 63 linesmodels/ _utils.py - feature_extraction/
onekey_core/ , Python, 232 linesmodels/ res2net_v1b.py - feature_extraction/
onekey_core/ , Python, 395 linesmodels/ resnet.py - feature_extraction/
onekey_core/ , Python, 227 linesmodels/ resnet3d.py - feature_extraction/
onekey_core/ , Python, 4 linesmodels/ utils.py - feature_extraction/
onekey_core/ , Python, 1 linetransforms/ __init__.py - feature_extraction/
onekey_core/ , Python, 846 linestransforms/ functional.py - feature_extraction/
onekey_core/ , Python, 1,295 linestransforms/ transforms.py - feature_extraction/
onekey_core/ , Python, 107 linesutils.py - quality_supervision/
create_patch_dataset_csv , Python, 20 lines.py - quality_supervision/
patch_quality_supervisio , Python, 75 linesn.py - quality_supervision/
patch_reading.py , Python, 51 lines - quality_supervision/
quality_supervision_mode , Python, 38 linesl.py - LICENSE, License, 1 line
- README.md, Text, 147 lines
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Cite
This paper
Ma, J., Yao, Q., Fu, X., Xia, Z., Yue, Y., Xu, D., Yuan, X., Zhao, L., Wang, J., Dong, A., Gao, L., Yang, J., Shen, L., Zheng, Y., & Ni, S. (2026). Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology. Journal of translational medicine, 24(1), 691. https://
BibTeX
@article{ma2026interpret
author = {Ma, Juan and Yao, Qiang and Fu, Xiaoying and Xia, Zhouqi and Yue, Yaoting and Xu, Dongqing and Yuan, Xiaojun and Zhao, Liebin and Wang, Jinhu and Dong, Ao and Gao, Limei and Yang, Junyao and Shen, Lisong and Zheng, Yingxia and Ni, Shaoqing},
title = {{Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology}},
journal = {Journal of translational medicine},
year = {2026},
month = apr,
volume = {24},
number = {1},
pages = {691},
publisher = {BMC},
issn = {1479-5876},
doi = {10.1186/
url = {https://
pmid = {41947227},
pmcid = {PMC13188757}
}
RIS
TY - JOUR
AU - Ma, Juan
AU - Yao, Qiang
AU - Fu, Xiaoying
AU - Xia, Zhouqi
AU - Yue, Yaoting
AU - Xu, Dongqing
AU - Yuan, Xiaojun
AU - Zhao, Liebin
AU - Wang, Jinhu
AU - Dong, Ao
AU - Gao, Limei
AU - Yang, Junyao
AU - Shen, Lisong
AU - Zheng, Yingxia
AU - Ni, Shaoqing
TI - Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology
T2 - Journal of translational medicine
J2 - J Transl Med
PY - 2026
DA - 2026/
VL - 24
IS - 1
SP - 691
SN - 1479-5876
PB - BMC
DO - 10.1186/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1186/
"type": "article-journal",
"title": "Interpretative diagnostic model for neuroblastoma metastases using bone marrow cytology",
"container-title": "Journal of translational medicine",
"author": [
{
"family": "Ma",
"given": "Juan"
},
{
"family": "Yao",
"given": "Qiang"
},
{
"family": "Fu",
"given": "Xiaoying"
},
{
"family": "Xia",
"given": "Zhouqi"
},
{
"family": "Yue",
"given": "Yaoting"
},
{
"family": "Xu",
"given": "Dongqing"
},
{
"family": "Yuan",
"given": "Xiaojun"
},
{
"family": "Zhao",
"given": "Liebin"
},
{
"family": "Wang",
"given": "Jinhu"
},
{
"family": "Dong",
"given": "Ao"
},
{
"family": "Gao",
"given": "Limei"
},
{
"family": "Yang",
"given": "Junyao"
},
{
"family": "Shen",
"given": "Lisong"
},
{
"family": "Zheng",
"given": "Yingxia"
},
{
"family": "Ni",
"given": "Shaoqing"
}
],
"container-title-short":
"volume": "24",
"issue": "1",
"page": "691",
"DOI": "10.1186/
"PMID": "41947227",
"PMCID": "PMC13188757",
"ISSN": "1479-5876",
"publisher": "BMC",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
4,
7
]
]
}
}
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