In the study of the deep learning classification of medical images, deep learning models are applied to analyze images, aiming to achieve the goals of assisting diagnosis and preoperative assessment. Currently, most research classifies and predicts normal and cancer cells by inputting single-parameter images into trained models. However, for ovarian cancer (OC), identifying its different subtypes is crucial for predicting disease prognosis. In particular, the need to distinguish high-grade serous carcinoma from clear cell carcinoma preoperatively through non-invasive means has not been fully addressed. This study proposes a deep learning (DL) method based on the fusion of multi-parametric magnetic resonance imaging (mpMRI) data, aimed at improving the accuracy of preoperative ovarian cancer subtype classification. By constructing a new deep learning network architecture that integrates various sequence features, this architecture achieves the high-precision prediction of the typing of high-grade serous carcinoma and clear cell carcinoma, achieving an AUC of 91.62% and an AP of 95.13% in the classification of ovarian cancer subtypes.

In a biological signal analysis system, signals of the same type may exhibit significant variations in their feature waveforms. Biological signals are typically weak, which increases the complexity of their analysis. Furthermore, clinical biomedical signals are susceptible to various interferences from the human body itself, including muscle movements, respiration, and heartbeat. These interference factors further escalate the complexity and difficulty of signal analysis. Therefore, precise and targeted preprocessing is often required before analyzing these clinical biomedical signals to enhance the accuracy and reliability of subsequent feature extraction and classification. Here, we have established an effective and practical algorithm model that integrates preprocessing with the initial localization of target feature waveforms, achieving the following four objectives: 1. Determining the periodic positions of target feature waveforms. 2. Preserving the original amplitude and shape of target feature waveforms while eliminating negative interference. 3. Reducing or eliminating interference from other feature waveforms in the input signal. 4. Decreasing noise in the input signal, such as baseline drift, powerline interference, and muscle artifacts commonly found in biological signals. We have validated the algorithm on clinical electrocardiogram (ECG) data and the authoritative MIT-BIH open-source ECG database demonstrating its effectiveness and reliability.