SwinMM: Masked Multi-view with Swin Transformers for 3D Medical Image Segmentation

Recent advancements in large-scale Vision Transformers have made significant strides in improving pre-trained models for medical image segmentation. However, these methods face a notable challenge in acquiring a substantial amount of pre-training data, particularly within the medical field. To address this limitation, we present Masked Multi-view with Swin Transformers (SwinMM), a novel multi-view pipeline for enabling accurate and data-efficient self-supervised medical image analysis. Our strategy harnesses the potential of multi-view information by incorporating two principal components. In the pre-training phase, we deploy a masked multi-view encoder devised to concurrently train masked multi-view observations through a range of diverse proxy tasks. These tasks span image reconstruction, rotation, contrastive learning, and a novel task that employs a mutual learning paradigm. This new task capitalizes on the consistency between predictions from various perspectives, enabling the extraction of hidden multi-view information from 3D medical data. In the fine-tuning stage, a cross-view decoder is developed to aggregate the multi-view information through a cross-attention block. Compared with the previous state-of-the-art self-supervised learning method Swin UNETR, SwinMM demonstrates a notable advantage on several medical image segmentation tasks. It allows for a smooth integration of multi-view information, significantly boosting both the accuracy and data-efficiency of the model. Code and models are available at https://github.com/UCSC-VLAA/SwinMM/.Comment: MICCAI 2023; project page: https://github.com/UCSC-VLAA/SwinMM

Supervised Learning Based Hypothesis Generation from Biomedical Literature

Nowadays, the amount of biomedical literatures is growing at an explosive speed, and there is much useful knowledge undiscovered in this literature. Researchers can form biomedical hypotheses through mining these works. In this paper, we propose a supervised learning based approach to generate hypotheses from biomedical literature. This approach splits the traditional processing of hypothesis generation with classic ABC model into AB model and BC model which are constructed with supervised learning method. Compared with the concept cooccurrence and grammar engineering-based approaches like SemRep, machine learning based models usually can achieve better performance in information extraction (IE) from texts. Then through combining the two models, the approach reconstructs the ABC model and generates biomedical hypotheses from literature. The experimental results on the three classic Swanson hypotheses show that our approach outperforms SemRep system

Relation path feature embedding based convolutional neural network method for drug discovery

Abstract Background Drug development is an expensive and time-consuming process. Literature-based discovery has played a critical role in drug development and may be a supplementary method to help scientists speed up the discovery of drugs. Methods Here, we propose a relation path features embedding based convolutional neural network model with attention mechanism for drug discovery from literature, which we denote as PACNN. First, we use predications from biomedical abstracts to construct a biomedical knowledge graph, and then apply a path ranking algorithm to extract drug-disease relation path features on the biomedical knowledge graph. After that, we use these drug-disease relation features to train a convolutional neural network model which combined with the attention mechanism. Finally, we employ the trained models to mine drugs for treating diseases. Results The experiment shows that the proposed model achieved promising results, comparing to several random walk algorithms. Conclusions In this paper, we propose a relation path features embedding based convolutional neural network with attention mechanism for discovering potential drugs from literature. Our method could be an auxiliary method for drug discovery, which can speed up the discovery of new drugs for the incurable diseases

SemaTyP: a knowledge graph based literature mining method for drug discovery

Abstract Background Drug discovery is the process through which potential new medicines are identified. High-throughput screening and computer-aided drug discovery/design are the two main drug discovery methods for now, which have successfully discovered a series of drugs. However, development of new drugs is still an extremely time-consuming and expensive process. Biomedical literature contains important clues for the identification of potential treatments. It could support experts in biomedicine on their way towards new discoveries. Methods Here, we propose a biomedical knowledge graph-based drug discovery method called SemaTyP, which discovers candidate drugs for diseases by mining published biomedical literature. We first construct a biomedical knowledge graph with the relations extracted from biomedical abstracts, then a logistic regression model is trained by learning the semantic types of paths of known drug therapies’ existing in the biomedical knowledge graph, finally the learned model is used to discover drug therapies for new diseases. Results The experimental results show that our method could not only effectively discover new drug therapies for new diseases, but also could provide the potential mechanism of action of the candidate drugs. Conclusions In this paper we propose a novel knowledge graph based literature mining method for drug discovery. It could be a supplementary method for current drug discovery methods

Identifying protein complexes based on node embeddings obtained from protein-protein interaction networks

Abstract Background Protein complexes are one of the keys to deciphering the behavior of a cell system. During the past decade, most computational approaches used to identify protein complexes have been based on discovering densely connected subgraphs in protein-protein interaction (PPI) networks. However, many true complexes are not dense subgraphs and these approaches show limited performances for detecting protein complexes from PPI networks. Results To solve these problems, in this paper we propose a supervised learning method based on network node embeddings which utilizes the informative properties of known complexes to guide the search process for new protein complexes. First, node embeddings are obtained from human protein interaction network. Then the protein interactions are weighted through the similarities between node embeddings. After that, the supervised learning method is used to detect protein complexes. Then the random forest model is used to filter the candidate complexes in order to obtain the final predicted complexes. Experimental results on real human and yeast protein interaction networks show that our method effectively improves the performance for protein complex detection. Conclusions We provided a new method for identifying protein complexes from human and yeast protein interaction networks, which has great potential to benefit the field of protein complex detection

Additional file 2 of SemaTyP: a knowledge graph based literature mining method for drug discovery

Supplementary Data 2. The gold standard drug-disease cases extracted from TTD. There are 360 drug-disease relationships are selected from TTD as gold standard to form test data for drug rediscovery test. Each disease i in test set has one known associated drug i , but the drug mechanism of action is unclear. (TXT 10 kb

Additional file 2: of A method for predicting protein complex in dynamic PPI networks

Krogan PPI data. (TXT 117 kb

Additional file 1 of SemaTyP: a knowledge graph based literature mining method for drug discovery

Supplementary Data 1. The gold standard drug-target-disease cases used in this work. The 7144 drug-target-disease cases which are extracted from Therapeutic Target Database (TTD) as true cases for constructing training data. (TXT 466 kb

Disease gene prediction based on heterogeneous probabilistic hypergraph ranking

In order to save time and cost, many disease gene prediction methods have been proposed in recent years. However, the traditional network model uses a binary relationship to represent the relationship between different proteins or gene molecules and phenotypes, which leads to the loss of information. Recently, hypergraph shows that it can overcome this loss of information to some extent and preserve the multivariate relationship, so we transformed the disease gene prediction problem into the problem of ranking the multivariate-relationship object. In this paper, we propose a method of Heterogeneous Probabilistic Hypergraph Ranking (HPHR) to predict disease genes. Firstly, fix a graph centroid for each hyperedge and according to different associations, and add other nodes related to the graph centroid to hyperedges with a certain probability. Then transform the problem of predicting disease genes into the problem of ranking heterogeneous objects, and the candidate genes are sorted by hypergraph ranking. The method is then applied to the integrated disease gene network. Compared with other prediction methods achieved better results, which was verified by this experiment