Heterogeneous Causal Metapath Graph Neural Network for Gene-Microbe-Disease Association Prediction
- URL: http://arxiv.org/abs/2406.19156v1
- Date: Thu, 27 Jun 2024 13:17:33 GMT
- Title: Heterogeneous Causal Metapath Graph Neural Network for Gene-Microbe-Disease Association Prediction
- Authors: Kexin Zhang, Feng Huang, Luotao Liu, Zhankun Xiong, Hongyu Zhang, Yuan Quan, Wen Zhang,
- Abstract summary: We propose a Heterogeneous Causal Metapath Graph Neural Network to predict gene-microbe-disease associations.
Our experiments show that HCMGNN effectively predicts GMD associations and addresses association sparsity issue.
- Score: 12.538590171093764
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: The recent focus on microbes in human medicine highlights their potential role in the genetic framework of diseases. To decode the complex interactions among genes, microbes, and diseases, computational predictions of gene-microbe-disease (GMD) associations are crucial. Existing methods primarily address gene-disease and microbe-disease associations, but the more intricate triple-wise GMD associations remain less explored. In this paper, we propose a Heterogeneous Causal Metapath Graph Neural Network (HCMGNN) to predict GMD associations. HCMGNN constructs a heterogeneous graph linking genes, microbes, and diseases through their pairwise associations, and utilizes six predefined causal metapaths to extract directed causal subgraphs, which facilitate the multi-view analysis of causal relations among three entity types. Within each subgraph, we employ a causal semantic sharing message passing network for node representation learning, coupled with an attentive fusion method to integrate these representations for predicting GMD associations. Our extensive experiments show that HCMGNN effectively predicts GMD associations and addresses association sparsity issue by enhancing the graph's semantics and structure.
Related papers
- Comprehensive Metapath-based Heterogeneous Graph Transformer for Gene-Disease Association Prediction [19.803593399456823]
COmprehensive MEtapath-based heterogeneous graph Transformer(COMET) for predicting gene-disease associations.
Our method demonstrates superior robustness compared to state-of-the-art approaches.
arXiv Detail & Related papers (2025-01-14T09:41:18Z) - Gene-Metabolite Association Prediction with Interactive Knowledge Transfer Enhanced Graph for Metabolite Production [49.814615043389864]
We propose a new task, Gene-Metabolite Association Prediction based on metabolic graphs.
We present the first benchmark containing 2474 metabolites and 1947 genes of two commonly used microorganisms.
Our proposed methodology outperforms baselines by up to 12.3% across various link prediction frameworks.
arXiv Detail & Related papers (2024-10-24T06:54:27Z) - Predicting Genetic Mutation from Whole Slide Images via Biomedical-Linguistic Knowledge Enhanced Multi-label Classification [119.13058298388101]
We develop a Biological-knowledge enhanced PathGenomic multi-label Transformer to improve genetic mutation prediction performances.
BPGT first establishes a novel gene encoder that constructs gene priors by two carefully designed modules.
BPGT then designs a label decoder that finally performs genetic mutation prediction by two tailored modules.
arXiv Detail & Related papers (2024-06-05T06:42:27Z) - Knowledge Graph Completion based on Tensor Decomposition for Disease
Gene Prediction [2.838553480267889]
We construct a biological knowledge graph centered on diseases and genes, and develop an end-to-end Knowledge graph completion model for Disease Gene Prediction.
KDGene introduces an interaction module between the embeddings of entities and relations to tensor decomposition, which can effectively enhance the information interaction in biological knowledge.
arXiv Detail & Related papers (2023-02-18T13:57:44Z) - Unsupervised ensemble-based phenotyping helps enhance the
discoverability of genes related to heart morphology [57.25098075813054]
We propose a new framework for gene discovery entitled Un Phenotype Ensembles.
It builds a redundant yet highly expressive representation by pooling a set of phenotypes learned in an unsupervised manner.
These phenotypes are then analyzed via (GWAS), retaining only highly confident and stable associations.
arXiv Detail & Related papers (2023-01-07T18:36:44Z) - Granger causal inference on DAGs identifies genomic loci regulating
transcription [77.58911272503771]
GrID-Net is a framework based on graph neural networks with lagged message passing for Granger causal inference on DAG-structured systems.
Our application is the analysis of single-cell multimodal data to identify genomic loci that mediate the regulation of specific genes.
arXiv Detail & Related papers (2022-10-18T21:15:10Z) - Graph Neural Networks for Microbial Genome Recovery [64.91162205624848]
We propose to use Graph Neural Networks (GNNs) to leverage the assembly graph when learning contig representations for metagenomic binning.
Our method, VaeG-Bin, combines variational autoencoders for learning latent representations of the individual contigs, with GNNs for refining these representations by taking into account the neighborhood structure of the contigs in the assembly graph.
arXiv Detail & Related papers (2022-04-26T12:49:51Z) - Graph Representation Learning on Tissue-Specific Multi-Omics [0.0]
We leverage a graph embedding model (i.e VGAE) to perform link prediction on tissue-specific Gene-Gene Interaction (GGI) networks.
We prove that the combination of multiple biological modalities (i.e multi-omics) leads to powerful embeddings and better link prediction performances.
arXiv Detail & Related papers (2021-07-25T17:38:45Z) - Interpretable Drug Synergy Prediction with Graph Neural Networks for
Human-AI Collaboration in Healthcare [23.151336811933938]
We propose a deep graph neural network, IDSP, to incorporate the gene-gene as well as gene-drug regulatory relationships in synergic drug combination predictions.
IDSP automatically learns weights of edges based on the gene and drug node relations, by a multi-layer perceptron (MLP) and aggregates information in an inductive manner.
We test IDWSP on signaling networks formulated by genes from 46 core cancer signaling pathways and drug combinations from NCI ALMANAC drug combination screening data.
arXiv Detail & Related papers (2021-05-14T22:20:29Z) - Relation-weighted Link Prediction for Disease Gene Identification [0.3078691410268859]
We propose a novel machine learning method that identifies disease genes on such graphs.
We show that our algorithms outperform its closest state-of-the-art competitor in disease gene identification by 24.1%.
We also show that we achieve higher precision than Open Targets, the leading initiative for target identification, with respect to predicting drug targets in clinical trials for Parkinson's disease.
arXiv Detail & Related papers (2020-11-10T15:09:33Z) - A Graph Gaussian Embedding Method for Predicting Alzheimer's Disease
Progression with MEG Brain Networks [59.15734147867412]
Characterizing the subtle changes of functional brain networks associated with Alzheimer's disease (AD) is important for early diagnosis and prediction of disease progression.
We developed a new deep learning method, termed multiple graph Gaussian embedding model (MG2G)
We used MG2G to detect the intrinsic latent dimensionality of MEG brain networks, predict the progression of patients with mild cognitive impairment (MCI) to AD, and identify brain regions with network alterations related to MCI.
arXiv Detail & Related papers (2020-05-08T02:29:24Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.