<abstract><p>The prediction of drug-target protein interaction (DTI) is a crucial task in the development of new drugs in modern medicine. Accurately identifying DTI through computer simulations can significantly reduce development time and costs. In recent years, many sequence-based DTI prediction methods have been proposed, and introducing attention mechanisms has improved their forecasting performance. However, these methods have some shortcomings. For example, inappropriate dataset partitioning during data preprocessing can lead to overly optimistic prediction results. Additionally, only single non-covalent intermolecular interactions are considered in the DTI simulation, ignoring the complex interactions between their internal atoms and amino acids. In this paper, we propose a network model called Mutual-DTI that predicts DTI based on the interaction properties of sequences and a Transformer model. We use multi-head attention to extract the long-distance interdependent features of the sequence and introduce a module to extract the sequence's mutual interaction features in mining complex reaction processes of atoms and amino acids. We evaluate the experiments on two benchmark datasets, and the results show that Mutual-DTI outperforms the latest baseline significantly. In addition, we conduct ablation experiments on a label-inversion dataset that is split more rigorously. The results show that there is a significant improvement in the evaluation metrics after introducing the extracted sequence interaction feature module. This suggests that Mutual-DTI may contribute to modern medical drug development research. The experimental results show the effectiveness of our approach. The code for Mutual-DTI can be downloaded from <ext-link ext-link-type="uri" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="https://github.com/a610lab/Mutual-DTI">https://github.com/a610lab/Mutual-DTI</ext-link>.</p></abstract>

<abstract> <p>Ultrasound computed tomography (USCT) has been developed for breast tumor screening. The sound-speed modal of USCT can provide quantitative sound-speed values to help tumor diagnosis. Time-of-flight (TOF) is the critical input in sound-speed reconstruction. However, we found that the missing data problem in the detected TOF causes artifacts on the reconstructed sound-speed images, which may affect the tumor identification. In this study, to address the missing TOF data problem, we first adopted the singular value threshold (SVT) algorithm to complete the TOF matrix. The threshold value in SVT is difficult to determine, so we proposed a selection strategy, that is, to enumerate the threshold values as the multiples of the maximum singular value of the incomplete matrix and then evaluate the image quality to select the proper threshold value. In the numerical breast phantom experiment, the artifacts are eliminated, and the accuracy is higher than the accuracy of the compared methods. In the in vivo experiment, we reconstructed the sound-speed image of the breast of a volunteer with invasive breast cancer, and the SVT algorithm improved the image sharpness. The completion of DTOF based on SVT gives better accuracy than the compared methods, but too large a threshold value decreases the accuracy. In the future, the selection method of the threshold value needs further research, and more USCT cases should be included in the experiments.</p> </abstract>