Functional data analysis (FDA) is essential for analyzing continuous, high-dimensional data, yet existing methods often decouple functional registration and classification, limiting their efficiency and performance. We present DeepFRC, an end-to-end deep learning framework that unifies these tasks within a single model. Our approach incorporates an alignment module that learns time warping functions via elastic function registration and a learnable basis representation module for dimensionality reduction on aligned data. This integration enhances both alignment accuracy and predictive performance. Theoretical analysis establishes that DeepFRC achieves low misalignment and generalization error, while simulations elucidate the progression of registration, reconstruction, and classification during training. Experiments on real-world datasets demonstrate that DeepFRC consistently outperforms state-of-the-art methods, particularly in addressing complex registration challenges. Code is available at: https://github.com/Drivergo-93589/DeepFRC.

Large Language Models (LLMs) have been widely used in code completion, and researchers are focusing on scaling up LLMs to improve their accuracy. However, larger LLMs will increase the response time of code completion and decrease the developers' productivity. In this paper, we propose a lightweight and effective LLM for code completion named aiXcoder-7B. Compared to existing LLMs, aiXcoder-7B achieves higher code completion accuracy while having smaller scales (i.e., 7 billion parameters). We attribute the superiority of aiXcoder-7B to three key factors: (1) Multi-objective training. We employ three training objectives, one of which is our proposed Structured Fill-In-the-Middle (SFIM). SFIM considers the syntax structures in code and effectively improves the performance of LLMs for code. (2) Diverse data sampling strategies. They consider inter-file relationships and enhance the capability of LLMs in understanding cross-file contexts. (3) Extensive high-quality data. We establish a rigorous data collection pipeline and consume a total of 1.2 trillion unique tokens for training aiXcoder-7B. This vast volume of data enables aiXcoder-7B to learn a broad distribution of code. We evaluate aiXcoder-7B in five popular code completion benchmarks and a new benchmark collected by this paper. The results show that aiXcoder-7B outperforms the latest six LLMs with similar sizes and even surpasses four larger LLMs (e.g., StarCoder2-15B and CodeLlama-34B), positioning aiXcoder-7B as a lightweight and effective LLM for academia and industry. Finally, we summarize three valuable insights for helping practitioners train the next generations of LLMs for code. aiXcoder-7B has been open-souced and gained significant attention. As of the submission date, aiXcoder-7B has received 2,193 GitHub Stars.

Ultrasound is a vital diagnostic technique in health screening, with the advantages of non-invasive, cost-effective, and radiation free, and therefore is widely applied in the diagnosis of nodules. However, it relies heavily on the expertise and clinical experience of the sonographer. In ultrasound images, a single nodule might present heterogeneous appearances in different cross-sectional views which makes it hard to perform per-nodule examination. Sonographers usually discriminate different nodules by examining the nodule features and the surrounding structures like gland and duct, which is cumbersome and time-consuming. To address this problem, we collected hundreds of breast ultrasound videos and built a nodule reidentification system that consists of two parts: an extractor based on the deep learning model that can extract feature vectors from the input video clips and a real-time clustering algorithm that automatically groups feature vectors by nodules. The system obtains satisfactory results and exhibits the capability to differentiate ultrasound videos. As far as we know, it's the first attempt to apply re-identification technique in the ultrasonic field.

Source code summarization is the task of writing natural language descriptions of source code behavior. Code summarization underpins software documentation for programmers. Short descriptions of code help programmers understand the program quickly without having to read the code itself. Lately, neural source code summarization has emerged as the frontier of research into automated code summarization techniques. By far the most popular targets for summarization are program subroutines. The idea, in a nutshell, is to train an encoder-decoder neural architecture using large sets of examples of subroutines extracted from code repositories. The encoder represents the code and the decoder represents the summary. However, most current approaches attempt to treat the subroutine as a single unit. For example, by taking the entire subroutine as input to a Transformer or RNN-based encoder. But code behavior tends to depend on the flow from statement to statement. Normally dynamic analysis may shed light on this flow, but dynamic analysis on hundreds of thousands of examples in large datasets is not practical. In this paper, we present a statement-based memory encoder that learns the important elements of flow during training, leading to a statement-based subroutine representation without the need for dynamic analysis. We implement our encoder for code summarization and demonstrate a significant improvement over the state-of-the-art.

Virtual screening, including molecular docking, plays an essential role in drug discovery. Many traditional and machine-learning based methods are available to fulfil the docking task. The traditional docking methods are normally extensively time-consuming, and their performance in blind docking remains to be improved. Although the runtime of docking based on machine learning is significantly decreased, their accuracy is still limited. In this study, we take the advantage of both traditional and machine-learning based methods, and present a method Deep Site and Docking Pose (DSDP) to improve the performance of blind docking. For the traditional blind docking, the entire protein is covered by a cube, and the initial positions of ligands are randomly generated in the cube. In contract, DSDP can predict the binding site of proteins and provide an accurate searching space and initial positions for the further conformational sampling. The docking task of DSDP makes use of the score function and a similar but modified searching strategy of AutoDock Vina, accelerated by implementation in GPUs. We systematically compare its performance with the state-of-the-art methods, including Autodock Vina, GNINA, QuickVina, SMINA, and DiffDock. DSDP reaches a 29.8% top-1 success rate (RMSD < 2 {\AA}) on an unbiased and challenging test dataset with 1.2 s wall-clock computational time per system. Its performances on DUD-E dataset and the time-split PDBBind dataset used in EquiBind, TankBind, and DiffDock are also effective, presenting a 57.2% and 41.8% top-1 success rate with 0.8 s and 1.0 s per system, respectively.