Recent advances in text-to-image (T2I) generation have led to impressive visual results. However, these models still face significant challenges when handling complex prompts-particularly those involving multiple subjects with distinct attributes. Inspired by the human drawing process, which first outlines the composition and then incrementally adds details, we propose Detail++, a training-free framework that introduces a novel Progressive Detail Injection (PDI) strategy to address this limitation. Specifically, we decompose a complex prompt into a sequence of simplified sub-prompts, guiding the generation process in stages. This staged generation leverages the inherent layout-controlling capacity of self-attention to first ensure global composition, followed by precise refinement. To achieve accurate binding between attributes and corresponding subjects, we exploit cross-attention mechanisms and further introduce a Centroid Alignment Loss at test time to reduce binding noise and enhance attribute consistency. Extensive experiments on T2I-CompBench and a newly constructed style composition benchmark demonstrate that Detail++ significantly outperforms existing methods, particularly in scenarios involving multiple objects and complex stylistic conditions.

Cloth-changing person re-identification aims at recognizing the same person with clothing changes across non-overlapping cameras. Advanced methods either resort to identity-related auxiliary modalities (e.g., sketches, silhouettes, and keypoints) or clothing labels to mitigate the impact of clothes. However, relying on unpractical and inflexible auxiliary modalities or annotations limits their real-world applicability. In this paper, we promote cloth-changing person re-identification by leveraging abundant semantics present within pedestrian images, without the need for any auxiliaries. Specifically, we first propose a unified Semantics Mining and Refinement (SMR) module to extract robust identity-related content and salient semantics, mitigating interference from clothing appearances effectively. We further propose the Content and Salient Semantics Collaboration (CSSC) framework to collaborate and leverage various semantics, facilitating cross-parallel semantic interaction and refinement. Our proposed method achieves state-of-the-art performance on three cloth-changing benchmarks, demonstrating its superiority over advanced competitors. The code is available at https://github.com/QizaoWang/CSSC-CCReID.

Financial crime detection using graph learning improves financial safety and efficiency. However, criminals may commit financial crimes across different institutions to avoid detection, which increases the difficulty of detection for financial institutions which use local data for graph learning. As most financial institutions are subject to strict regulations in regards to data privacy protection, the training data is often isolated and conventional learning technology cannot handle the problem. Federated learning (FL) allows multiple institutions to train a model without revealing their datasets to each other, hence ensuring data privacy protection. In this paper, we proposes a novel two-stage approach to federated graph learning (2SFGL): The first stage of 2SFGL involves the virtual fusion of multiparty graphs, and the second involves model training and inference on the virtual graph. We evaluate our framework on a conventional fraud detection task based on the FraudAmazonDataset and FraudYelpDataset. Experimental results show that integrating and applying a GCN (Graph Convolutional Network) with our 2SFGL framework to the same task results in a 17.6%-30.2% increase in performance on several typical metrics compared to the case only using FedAvg, while integrating GraphSAGE with 2SFGL results in a 6%-16.2% increase in performance compared to the case only using FedAvg. We conclude that our proposed framework is a robust and simple protocol which can be simply integrated to pre-existing graph-based fraud detection methods.

Vision-and-language navigation (VLN), a frontier study aiming to pave the way for general-purpose robots, has been a hot topic in the computer vision and natural language processing community. The VLN task requires an agent to navigate to a goal location following natural language instructions in unfamiliar environments.

In this paper, an improve rate control algorithm for H.264 is proposed which takes image complexity and motion information into consideration to predict the Mean Absolute Difference (MAD). The changes of MAD are adopted to represent the image complexity, and compute the target bit of the current basic unit. Experimental results show that compared with the algorithms of JVT-G012, the bitrate of proposed algorithm is closer to the target bit, and the average of peak signal to noise ratio (PSNR) is improved 0.2183dB.

BACKGROUND: Existing large-scale metabolic models of sequenced organisms commonly include enzymatic functions which can not be attributed to any gene in that organism. Existing computational strategies for identifying such missing genes rely primarily on sequence homology to known enzyme-encoding genes. RESULTS: We present a novel method for identifying genes encoding for a specific metabolic function based on a local structure of metabolic network and multiple types of functional association evidence, including clustering of genes on the chromosome, similarity of phylogenetic profiles, gene expression, protein fusion events and others. Using E. coli and S. cerevisiae metabolic networks, we illustrate predictive ability of each individual type of association evidence and show that significantly better predictions can be obtained based on the combination of all data. In this way our method is able to predict 60% of enzyme-encoding genes of E. coli metabolism within the top 10 (out of 3551) candidates for their enzymatic function, and as a top candidate within 43% of the cases. CONCLUSION: We illustrate that a combination of genome context and other functional association evidence is effective in predicting genes encoding metabolic enzymes. Our approach does not rely on direct sequence homology to known enzyme-encoding genes, and can be used in conjunction with traditional homology-based metabolic reconstruction methods. The method can also be used to target orphan metabolic activities.

MOTIVATION: With more and more scientific literature published online, the effective management and reuse of this knowledge has become problematic. Natural language processing (NLP) may be a potential solution by extracting, structuring and organizing biomedical information in online literature in a timely manner. One essential task is to recognize and identify genomic entities in text. 'Recognition' can be accomplished using pattern matching and machine learning. But for 'identification' these techniques are not adequate. In order to identify genomic entities, NLP needs a comprehensive resource that specifies and classifies genomic entities as they occur in text and that associates them with normalized terms and also unique identifiers so that the extracted entities are well defined. Online organism databases are an excellent resource to create such a lexical resource. However, gene name ambiguity is a serious problem because it affects the appropriate identification of gene entities. In this paper, we explore the extent of the problem and suggest ways to address it. RESULTS: We obtained gene information from 21 organisms and quantified naming ambiguities within species, across species, with English words and with medical terms. When the case (of letters) was retained, official symbols displayed negligible intra-species ambiguity (0.02%) and modest ambiguities with general English words (0.57%) and medical terms (1.01%). In contrast, the across-species ambiguity was high (14.20%). The inclusion of gene synonyms increased intra-species ambiguity substantially and full names contributed greatly to gene-medical-term ambiguity. A comprehensive lexical resource that covers gene information for the 21 organisms was then created and used to identify gene names by using a straightforward string matching program to process 45,000 abstracts associated with the mouse model organism while ignoring case and gene names that were also English words. We found that 85.1% of correctly retrieved mouse genes were ambiguous with other gene names. When gene names that were also English words were included, 233% additional 'gene' instances were retrieved, most of which were false positives. We also found that authors prefer to use synonyms (74.7%) to official symbols (17.7%) or full names (7.6%) in their publications. CONTACT: [email protected]