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Jiancheng Xu

Publications and source records attributed to Jiancheng Xu.

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F10.7 Index Prediction: A Multiscale Decomposition Strategy with Wavelet Transform for Performance Optimization

In this study, we construct Dataset A for training, validation, and testing, and Dataset B to evaluate generalization. We propose a novel F10.7 index forecasting method using wavelet decomposition, which feeds F10.7 together with its decomposed approximate and detail signals into the iTransformer model. We also incorporate the International Sunspot Number (ISN) and its wavelet-decomposed signals to assess their influence on prediction performance. Our optimal method is then compared with the latest method from S. Yan et al. (2025) and three operational models (SWPC, BGS, CLS). Additionally, we transfer our method to the PatchTST model used in H. Ye et al. (2024) and compare our method with theirs on Dataset B. Key findings include: (1) The wavelet-based combination methods overall outperform the baseline using only F10.7 index. The prediction performance improves as higher-level approximate and detail signals are incrementally added. The Combination 6 method integrating F10.7 with its first to fifth level approximate and detail signals outperforms methods using only approximate or detail signals. (2) Incorporating ISN and its wavelet-decomposed signals does not enhance prediction performance. (3) The Combination 6 method significantly surpasses S. Yan et al. (2025) and three operational models, with RMSE, MAE, and MAPE reduced by 18.22%, 15.09%, and 8.57%, respectively, against the former method. It also excels across four different conditions of solar activity. (4) Our method demonstrates superior generalization and prediction capability over the method of H. Ye et al. (2024) across all forecast horizons. To our knowledge, this is the first application of wavelet decomposition in F10.7 prediction, substantially improving forecast performance.

astro-ph.IM

Establishment of a diagnostic model to distinguish coronavirus disease 2019 from influenza A based on laboratory findings

Background: Coronavirus disease 2019 (COVID-19) and Influenza A are common disease caused by viral infection. The clinical symptoms and transmission routes of the two diseases are similar. However, there are no relevant studies on laboratory diagnostic models to discriminate COVID-19 and influenza A. This study aims at establishing a signature of laboratory findings to tell patients with COVID-19 apart from those with influenza A perfectly. Materials: In this study, 56 COVID-19 patients and 54 influenza A patients were included. Laboratory findings, epidemiological characteristics and demographic data were obtained from electronic medical record databases. Elastic network models, followed by a stepwise logistic regression model were implemented to identify indicators capable of discriminating COVID-19 and influenza A. A nomogram is diagramed to show the resulting discriminative model. Results: The majority of hematological and biochemical parameters in COVID-19 patients were significantly different from those in influenza A patients. In the final model, albumin/globulin (A/G), total bilirubin (TBIL) and erythrocyte specific volume (HCT) were selected as predictors. Using an external dataset, the model was validated to perform well. Conclusion: A diagnostic model of laboratory findings was established, in which A/G, TBIL and HCT were included as highly relevant indicators for the segmentation of COVID-19 and influenza A, providing a complimentary means for the precise diagnosis of these two diseases.

q-bio.BM