To obtain high-quality positron emission tomography (PET) while minimizing radiation exposure, a range of methods have been designed to reconstruct standard-dose PET (SPET) from corresponding low-dose PET (LPET) images. However, most current methods merely learn the mapping between single-dose-level LPET and SPET images, but omit the dose disparity of LPET images in clinical scenarios. In this paper, to reconstruct high-quality SPET images from multi-dose-level LPET images, we design a novel two-phase multi-dose-level PET reconstruction algorithm with dose level awareness, containing a pre-training phase and a SPET prediction phase. Specifically, the pre-training phase is devised to explore both fine-grained discriminative features and effective semantic representation. The SPET prediction phase adopts a coarse prediction network utilizing pre-learned dose level prior to generate preliminary result, and a refinement network to precisely preserve the details. Experiments on MICCAI 2022 Ultra-low Dose PET Imaging Challenge Dataset have demonstrated the superiority of our method.
Deep learning has facilitated the automation of radiotherapy by predicting accurate dose distribution maps. However, existing methods fail to derive the desirable radiotherapy parameters that can be directly input into the treatment planning system (TPS), impeding the full automation of radiotherapy. To enable more thorough automatic radiotherapy, in this paper, we propose a novel two-stage framework to directly regress the radiotherapy parameters, including a dose map prediction stage and a radiotherapy parameters regression stage. In stage one, we combine transformer and convolutional neural network (CNN) to predict realistic dose maps with rich global and local information, providing accurate dosimetric knowledge for the subsequent parameters regression. In stage two, two elaborate modules, i.e., an intra-relation modeling (Intra-RM) module and an inter-relation modeling (Inter-RM) module, are designed to exploit the organ-specific and organ-shared features for precise parameters regression. Experimental results on a rectal cancer dataset demonstrate the effectiveness of our method.
Large context window is a desirable feature in large language models (LLMs). However, due to high fine-tuning costs, scarcity of long texts, and catastrophic values introduced by new token positions, current extended context windows are limited to around 128k tokens. This paper introduces LongRoPE that, for the first time, extends the context window of pre-trained LLMs to an impressive 2048k tokens, with up to only 1k fine-tuning steps at within 256k training lengths, while maintaining performance at the original short context window. This is achieved by three key innovations: (i) we identify and exploit two forms of non-uniformities in positional interpolation through an efficient search, providing a better initialization for fine-tuning and enabling an 8x extension in non-fine-tuning scenarios; (ii) we introduce a progressive extension strategy that first fine-tunes a 256k length LLM and then conducts a second positional interpolation on the fine-tuned extended LLM to achieve a 2048k context window; (iii) we readjust LongRoPE on 8k length to recover the short context window performance. Extensive experiments on LLaMA2 and Mistral across various tasks demonstrate the effectiveness of our method. Models extended via LongRoPE retain the original architecture with minor modifications to the positional embedding, and can reuse most pre-existing optimizations.
Radiotherapy is a primary treatment for cancers with the aim of applying sufficient radiation dose to the planning target volume (PTV) while minimizing dose hazards to the organs at risk (OARs). Convolutional neural networks (CNNs) have automated the radiotherapy plan-making by predicting the dose maps. However, current CNN-based methods ignore the remarkable dose difference in the dose map, i.e., high dose value in the interior PTV while low value in the exterior PTV, leading to a suboptimal prediction. In this paper, we propose a triplet-constraint transformer (TCtrans) with multi-scale refinement to predict the high-quality dose distribution. Concretely, a novel PTV-guided triplet constraint is designed to refine dose feature representations in the interior and exterior PTV by utilizing the explicit geometry of PTV. Furthermore, we introduce a multi-scale refinement (MSR) module to effectively fulfill the triplet constraint in different decoding layers with multiple scales. Besides, a transformer encoder is devised to learn the important global dosimetric knowledge. Experiments on a clinical cervical cancer dataset demonstrate the superiority of our method.
Industrial recommender systems usually consist of the retrieval stage and the ranking stage, to handle the billion-scale of users and items. The retrieval stage retrieves candidate items relevant to user interests for recommendations and has attracted much attention. Frequently, a user shows refined multi-interests in a hierarchical structure. For example, a user likes Conan and Kuroba Kaito, which are the roles in hierarchical structure "Animation, Japanese Animation, Detective Conan". However, most existing methods ignore this hierarchical nature, and simply average the fine-grained interest information. Therefore, we propose a novel two-stage approach to explicitly modeling refined multi-interest in a hierarchical structure for recommendation. In the first hierarchical multi-interest mining stage, the hierarchical clustering and transformer-based model adaptively generate circles or sub-circles that users are interested in. In the second stage, the partition of retrieval space allows the EBR models to deal only with items within each circle and accurately capture users' refined interests. Experimental results show that the proposed approach achieves state-of-the-art performance. Our framework has also been deployed at Lofter.
Deep learning (DL) has successfully automated dose distribution prediction in radiotherapy planning, enhancing both efficiency and quality. However, existing methods suffer from the over-smoothing problem for their commonly used L1 or L2 loss with posterior average calculations. To alleviate this limitation, we propose a diffusion model-based method (DiffDose) for predicting the radiotherapy dose distribution of cancer patients. Specifically, the DiffDose model contains a forward process and a reverse process. In the forward process, DiffDose transforms dose distribution maps into pure Gaussian noise by gradually adding small noise and a noise predictor is simultaneously trained to estimate the noise added at each timestep. In the reverse process, it removes the noise from the pure Gaussian noise in multiple steps with the well-trained noise predictor and finally outputs the predicted dose distribution maps...
Logical query answering over Knowledge Graphs (KGs) is a fundamental yet complex task. A promising approach to achieve this is to embed queries and entities jointly into the same embedding space. Research along this line suggests that using multi-modal distribution to represent answer entities is more suitable than uni-modal distribution, as a single query may contain multiple disjoint answer subsets due to the compositional nature of multi-hop queries and the varying latent semantics of relations. However, existing methods based on multi-modal distribution roughly represent each subset without capturing its accurate cardinality, or even degenerate into uni-modal distribution learning during the reasoning process due to the lack of an effective similarity measure. To better model queries with diversified answers, we propose Query2GMM for answering logical queries over knowledge graphs. In Query2GMM, we present the GMM embedding to represent each query using a univariate Gaussian Mixture Model (GMM). Each subset of a query is encoded by its cardinality, semantic center and dispersion degree, allowing for precise representation of multiple subsets. Then we design specific neural networks for each operator to handle the inherent complexity that comes with multi-modal distribution while alleviating the cascading errors. Last, we define a new similarity measure to assess the relationships between an entity and a query's multi-answer subsets, enabling effective multi-modal distribution learning for reasoning. Comprehensive experimental results show that Query2GMM outperforms the best competitor by an absolute average of $5.5\%$. The source code is available at \url{https://anonymous.4open.science/r/Query2GMM-C42F}.
Malware open-set recognition (MOSR) aims at jointly classifying malware samples from known families and detect the ones from novel unknown families, respectively. Existing works mostly rely on a well-trained classifier considering the predicted probabilities of each known family with a threshold-based detection to achieve the MOSR. However, our observation reveals that the feature distributions of malware samples are extremely similar to each other even between known and unknown families. Thus the obtained classifier may produce overly high probabilities of testing unknown samples toward known families and degrade the model performance. In this paper, we propose the Multi-modal Dual-Embedding Networks, dubbed MDENet, to take advantage of comprehensive malware features (i.e., malware images and malware sentences) from different modalities to enhance the diversity of malware feature space, which is more representative and discriminative for down-stream recognition. Last, to further guarantee the open-set recognition, we dually embed the fused multi-modal representation into one primary space and an associated sub-space, i.e., discriminative and exclusive spaces, with contrastive sampling and rho-bounded enclosing sphere regularizations, which resort to classification and detection, respectively. Moreover, we also enrich our previously proposed large-scaled malware dataset MAL-100 with multi-modal characteristics and contribute an improved version dubbed MAL-100+. Experimental results on the widely used malware dataset Mailing and the proposed MAL-100+ demonstrate the effectiveness of our method.
We study the challenging task of malware recognition on both known and novel unknown malware families, called malware open-set recognition (MOSR). Previous works usually assume the malware families are known to the classifier in a close-set scenario, i.e., testing families are the subset or at most identical to training families. However, novel unknown malware families frequently emerge in real-world applications, and as such, require to recognize malware instances in an open-set scenario, i.e., some unknown families are also included in the test-set, which has been rarely and non-thoroughly investigated in the cyber-security domain. One practical solution for MOSR may consider jointly classifying known and detecting unknown malware families by a single classifier (e.g., neural network) from the variance of the predicted probability distribution on known families. However, conventional well-trained classifiers usually tend to obtain overly high recognition probabilities in the outputs, especially when the instance feature distributions are similar to each other, e.g., unknown v.s. known malware families, and thus dramatically degrades the recognition on novel unknown malware families. In this paper, we propose a novel model that can conservatively synthesize malware instances to mimic unknown malware families and support a more robust training of the classifier. Moreover, we also build a new large-scale malware dataset, named MAL-100, to fill the gap of lacking large open-set malware benchmark dataset. Experimental results on two widely used malware datasets and our MAL-100 demonstrate the effectiveness of our model compared with other representative methods.