Modern internet platforms usually have different scenarios to provide rich recommendation services to meet the diverse demands of users. Cross-domain recommendation (CDR) and multi-domain recommendation (MDR) methods are widely used in such platforms to leverage rich auxiliary information from multiple domains. However, state-of-the-art CDR and MDR methods usually enforce some correlations between source and target embeddings on each user, ignoring the correlations between users in both domains. To address this problem, we adopt a relaxed contrastive loss, that employs the pairwise similarities in the source domain as relaxed labels, enforcing such inter-sample relations are reserved in a weighted manner in the target domain. The basic assumption behind such a design is that users with similar interests should be with similar interacted items in a rec- ommender system, and this work takes a step further to realize and specify such similarity modeling as collaborative signals encoded in both implicit embedding spaces. We validate the effectiveness of the proposed method on a large- scale public dataset and a real production dataset with over 700 million samples. We further experimentally show that the proposed embedding transfer method is generic, and can be plugged into any existing deep neural networks, such as YoutubeDNN and BERT4Rec. Currently, the proposed embedding transfer techniques have been successfully deployed in the Guess You Like in WeTV for the CDR/MDR task.

Thanks to the huge accumulation of Electronic Health Records (EHRs), numerous deep learning based predictive models were proposed for this task. Among them, most of the existing state-of-the-art (SOTA) models were built with recurrent neural networks (RNNs). Regardless of their success, RNN-based models mainly suffer from three limitations. (i) Accuracy: the prediction accuracy of RNN-based models drops quickly as the length of EHR sequences increases. (ii) Efficiency: the recurrence property of RNN-based models makes the computation parallelization impossible, and accordingly hurts the efficiency of such models in practice. (iii) Interpretability: the outputs of RNN-based models are difficult to explain due to the unexplainable nature of deep models. In this paper, we resort to the recently advanced attention mechanism to model the dependencies between inputs and outputs, which overcomes shortages of RNN-based models in accuracy and efficiency. As for interpretability, we model the relationships with two linear mappings from the input to the output, which account for two important factors—one is for context-aware information and the other is for time-aware representation—of capturing discriminative features in learning patient’s representations. We empirically demonstrate the effectiveness of the proposed model in both accuracy and computational efficiency, meanwhile, analyze and discuss the reasonability of each explanation approach.

Graph neural networks have been widely used in recent recommender systems, where negative sampling plays an important role. Existing negative sampling methods restrict the relationship between nodes as either hard positive pairs or hard negative pairs. This leads to the loss of structural information, and lacks the mechanism to generate positive pairs for nodes with few neighbors. To overcome limitations, we propose a novel soft link-based sampling method, namely MixDec Sampling, which consists of Mixup Sampling module and Decay Sampling module. The Mixup Sampling augments node features by synthesizing new nodes and soft links, which provides sufficient number of samples for nodes with few neighbors. The Decay Sampling strengthens the digestion of graph structure information by generating soft links for node embedding learning. To the best of our knowledge, we are the first to model sampling relationships between nodes by soft links in GNN-based recommender systems. Extensive experiments demonstrate that the proposed MixDec Sampling can significantly and consistently improve the recommendation performance of several representative GNN-based models on various recommendation benchmarks.

Low-shot (one/few-shot) segmentation has attracted increasing attention as it works well with limited annotation. State-of-the-art low-shot segmentation methods on natural images usually focus on implicit representation learning for each novel class, such as learning prototypes, deriving guidance features via masked average pooling, and segmenting using cosine similarity in feature space. We argue that low-shot segmentation on medical images should step further to explicitly learn dense correspondences between images to utilize the anatomical similarity. The core ideas are inspired by the classical practice of multi-atlas segmentation, where the indispensable parts of atlas-based segmentation, i.e., registration, label propagation, and label fusion are unified into a single framework in our work. Specifically, we propose two alternative baselines, i.e., the Siamese-Baseline and Individual-Difference-Aware Baseline, where the former is targeted at anatomically stable structures (such as brain tissues), and the latter possesses a strong generalization ability to organs suffering large morphological variations (such as abdominal organs). In summary, this work sets up a benchmark for low-shot 3D medical image segmentation and sheds light on further understanding of atlas-based few-shot segmentation.

We propose a Healthcare Graph Convolutional Network (HealGCN) to offer disease self-diagnosis service for online users based on Electronic Healthcare Records (EHRs). Two main challenges are focused in this paper for online disease diagnosis: (1) serving cold-start users via graph convolutional networks and (2) handling scarce clinical description via a symptom retrieval system. To this end, we first organize the EHR data into a heterogeneous graph that is capable of modeling complex interactions among users, symptoms and diseases, and tailor the graph representation learning towards disease diagnosis with an inductive learning paradigm. Then, we build a disease self-diagnosis system with a corresponding EHR Graph-based Symptom Retrieval System (GraphRet) that can search and provide a list of relevant alternative symptoms by tracing the predefined meta-paths. GraphRet helps enrich the seed symptom set through the EHR graph when confronting users with scarce descriptions, hence yield better diagnosis accuracy. At last, we validate the superiority of our model on a large-scale EHR dataset.

We introduce a one-shot segmentation method to alleviate the burden of manual annotation for medical images. The main idea is to treat one-shot segmentation as a classical atlas-based segmentation problem, where voxel-wise correspondence from the atlas to the unlabelled data is learned. Subsequently, segmentation label of the atlas can be transferred to the unlabelled data with the learned correspondence. However, since ground truth correspondence between images is usually unavailable, the learning system must be well-supervised to avoid mode collapse and convergence failure. To overcome this difficulty, we resort to the forward-backward consistency, which is widely used in correspondence problems, and additionally learn the backward correspondences from the warped atlases back to the original atlas. This cycle-correspondence learning design enables a variety of extra, cycle-consistency-based supervision signals to make the training process stable, while also boost the performance. We demonstrate the superiority of our method over both deep learning-based one-shot segmentation methods and a classical multi-atlas segmentation method via thorough experiments.

Building a predictive model based on historical Electronic Health Records (EHRs) for personalized healthcare has become an active research area. Benefiting from the powerful ability of feature extraction, deep learning (DL) approaches have achieved promising performance in many clinical prediction tasks. However, due to the lack of interpretability and trustworthiness, it is difficult to apply DL in real clinical cases of decision making. To address this, in this paper, we propose an interpretable and trustworthy predictive model~(INPREM) for healthcare. Firstly, INPREM is designed as a linear model for interpretability while encoding non-linear relationships into the learning weights for modeling the dependencies between and within each visit. This enables us to obtain the contribution matrix of the input variables, which is served as the evidence of the prediction result(s), and help physicians understand why the model gives such a prediction, thereby making the model more interpretable. Secondly, for trustworthiness, we place a random gate (which follows a Bernoulli distribution to turn on or off) over each weight of the model, as well as an additional branch to estimate data noises. With the help of the Monto Carlo sampling and an objective function accounting for data noises, the model can capture the uncertainty of each prediction. The captured uncertainty, in turn, allows physicians to know how confident the model is, thus making the model more trustworthy. We empirically demonstrate that the proposed INPREM outperforms existing approaches with a significant margin. A case study is also presented to show how the contribution matrix and the captured uncertainty are used to assist physicians in making robust decisions.

Coronavirus Disease 2019 (COVID-19) has rapidly spread worldwide since first reported. Timely diagnosis of COVID-19 is crucial both for disease control and patient care. Non-contrast thoracic computed tomography (CT) has been identified as an effective tool for the diagnosis, yet the disease outbreak has placed tremendous pressure on radiologists for reading the exams and may potentially lead to fatigue-related mis-diagnosis. Reliable automatic classification algorithms can be really helpful; however, they usually require a considerable number of COVID-19 cases for training, which is difficult to acquire in a timely manner. Meanwhile, how to effectively utilize the existing archive of non-COVID-19 data (the negative samples) in the presence of severe class imbalance is another challenge. In addition, the sudden disease outbreak necessitates fast algorithm development. In this work, we propose a novel approach for effective and efficient training of COVID-19 classification networks using a small number of COVID-19 CT exams and an archive of negative samples. Concretely, a novel self-supervised learning method is proposed to extract features from the COVID-19 and negative samples. Then, two kinds of soft-labels ('difficulty' and 'diversity') are generated for the negative samples by computing the earth mover's distances between the features of the negative and COVID-19 samples, from which data 'values' of the negative samples can be assessed. A pre-set number of negative samples are selected accordingly and fed to the neural network for training. Experimental results show that our approach can achieve superior performance using about half of the negative samples, substantially reducing model training time.

Fully convolutional neural networks have made promising progress in joint liver and liver tumor segmentation. Instead of following the debates over 2D versus 3D networks (for example, pursuing the balance between large-scale 2D pretraining and 3D context), in this paper, we novelly identify the wide variation in the ratio between intra- and inter-slice resolutions as a crucial obstacle to the performance. To tackle the mismatch between the intra- and inter-slice information, we propose a slice-aware 2.5D network that emphasizes extracting discriminative features utilizing not only in-plane semantics but also out-of-plane coherence for each separate slice. Specifically, we present a slice-wise multi-input multi-output architecture to instantiate such a design paradigm, which contains a Multi-Branch Decoder (MD) with a Slice-centric Attention Block (SAB) for learning slice-specific features and a Densely Connected Dice (DCD) loss to regularize the inter-slice predictions to be coherent and continuous. Based on the aforementioned innovations, we achieve state-of-the-art results on the MICCAI 2017 Liver Tumor Segmentation (LiTS) dataset. Besides, we also test our model on the ISBI 2019 Segmentation of THoracic Organs at Risk (SegTHOR) dataset, and the result proves the robustness and generalizability of the proposed method in other segmentation tasks.

The need for short-text classification arises in many text mining applications particularly health care applications. In such applications shorter texts mean linguistic ambiguity limits the semantic expression, which in turns would make typical methods fail to capture the exact semantics of the scarce words. This is particularly true in health care domains when the text contains domain-specific or infrequently appearing words, whose embedding can not be easily learned due to the lack of training data. Deep neural network has shown great potentials in boost the performance of such problems according to its strength on representation capacity. In this paper, we propose a bidirectional long short-term memory (BI-LSTM) recurrent network to address the short-text classification problem that can be used in two settings. Firstly when a knowledge dictionary is available we adopt the well-known attention mechanism to guide the training of network using the domain knowledge in the dictionary. Secondly, to address the cases when domain knowledge dictionary is not available, we present a multi-task model to jointly learn the domain knowledge dictionary and do the text classification task simultaneously. We apply our method to a real-world interactive healthcare system and an extensively public available ATIS dataset. The results show that our model can positively grasp the key point of the text and significantly outperforms many state-of-the-art baselines.

Active learning aims to reduce manual labeling efforts by proactively selecting the most informative unlabeled instances to query. In real-world scenarios, it's often more practical to query a batch of instances rather than a single one at each iteration. To achieve this we need to keep not only the informativeness of the instances but also their diversity. Many heuristic methods have been proposed to tackle batch mode active learning problems, however, they suffer from two limitations which if addressed would significantly improve the query strategy. Firstly, the similarity amongst instances is simply calculated using the feature vectors rather than being jointly learned with the classification model. This weakens the accuracy of the diversity measurement. Secondly, these methods usually exploit the decision boundary by querying the data points close to it. However, this can be inefficient when the labeled set is too small to reveal the true boundary. In this paper, we address both limitations by proposing a deep neural network based algorithm. In the training phase, a pairwise deep network is not only trained to perform classification, but also to project data points into another space, where the similarity can be more precisely measured. In the query selection phase, the learner selects a set of instances that are maximally uncertain and minimally redundant (exploitation), as well as are most diverse from the labeled instances (exploration). We evaluate the effectiveness of the proposed method on a variety of classification tasks: MNIST classification, opinion polarity detection, and heart failure prediction. Our method outperforms the baselines with both higher classification accuracy and faster convergence rate.

Comparing and identifying similar patients is a fundamental task in medical domains - an efficient technique can, for example, help doctors to track patient cohorts, compare the effectiveness of treatments, or predict medical outcomes. The goal of patient similarity learning is to derive a clinically meaningful measure to evaluate the similarity amongst patients represented by their key clinical indicators. However, it is challenging to learn such similarity, as medical data are usually high dimensional, heterogeneous, and complex. In addition, a desirable patient similarity is dependent on particular clinical settings, which implies supervised learning scheme is more useful in medical domains. To address these, in this paper we present a novel similarity learning approach formulated as the generalized Mahalanobis similarity function with pairwise constraints. Considering there always exists some features non-discriminative and contains redundant information, we encode a low-rank structure to our similarity function to perform feature selection. We evaluate the proposed model on both UCI benchmarks and a real clinical dataset for several medical tasks, including patient retrieval, classification, and cohort discovery. The results show that our similarity model significantly outperforms many state-of-the-art baselines, and is effective at removing noisy or redundant features.