用于基因-疾病关联预测的异构生物医学实体表征学习。

IF 6.8 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS Briefings in bioinformatics Pub Date : 2024-07-25 DOI:10.1093/bib/bbae380
Zhaohan Meng, Siwei Liu, Shangsong Liang, Bhautesh Jani, Zaiqiao Meng
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引用次数: 0

摘要

了解疾病的遗传基础是医学研究的一个基本方面,因为基因是遗传的典型单位,在生物功能中起着至关重要的作用。确定基因与疾病之间的关联对于诊断、预防、预后和药物开发至关重要。编码具有相似序列的蛋白质的基因往往与相关疾病有牵连,因为导致相同或相似疾病的蛋白质往往在序列上显示出有限的变化。预测基因与疾病的关联(GDA)需要对大量潜在候选基因进行耗时且昂贵的实验。虽然有人提出了使用传统机器学习算法和图神经网络预测基因与疾病之间关联的方法,但这些方法难以捕捉基因和疾病的深层语义信息,而且依赖于训练数据。为了缓解这一问题,我们提出了一种名为 FusionGDA 的新型 GDA 预测模型,它利用预训练阶段的融合模块来丰富由预训练语言模型编码的基因和疾病语义表征。多模态表征由融合模块生成,其中包括两个异构生物医学实体的丰富语义信息:蛋白质序列和疾病描述。随后,采用池化聚合策略来压缩多模态表征的维度。此外,FusionGDA 还采用了预训练阶段,利用对比学习损失,通过在大型公共 GDA 数据集上进行训练来提取潜在的基因和疾病特征。为了严格评估 FusionGDA 模型的有效性,我们在五个数据集上进行了综合实验,并在 DisGeNet-Eval 数据集上将我们提出的模型与五个具有竞争力的基线模型进行了比较。值得注意的是,我们的案例研究进一步证明了 FusionGDA 有效发现隐藏关联的能力。我们实验的完整代码和数据集可在 https://github.com/ZhaohanM/FusionGDA 上获取。
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Heterogeneous biomedical entity representation learning for gene-disease association prediction.

Understanding the genetic basis of disease is a fundamental aspect of medical research, as genes are the classic units of heredity and play a crucial role in biological function. Identifying associations between genes and diseases is critical for diagnosis, prevention, prognosis, and drug development. Genes that encode proteins with similar sequences are often implicated in related diseases, as proteins causing identical or similar diseases tend to show limited variation in their sequences. Predicting gene-disease association (GDA) requires time-consuming and expensive experiments on a large number of potential candidate genes. Although methods have been proposed to predict associations between genes and diseases using traditional machine learning algorithms and graph neural networks, these approaches struggle to capture the deep semantic information within the genes and diseases and are dependent on training data. To alleviate this issue, we propose a novel GDA prediction model named FusionGDA, which utilizes a pre-training phase with a fusion module to enrich the gene and disease semantic representations encoded by pre-trained language models. Multi-modal representations are generated by the fusion module, which includes rich semantic information about two heterogeneous biomedical entities: protein sequences and disease descriptions. Subsequently, the pooling aggregation strategy is adopted to compress the dimensions of the multi-modal representation. In addition, FusionGDA employs a pre-training phase leveraging a contrastive learning loss to extract potential gene and disease features by training on a large public GDA dataset. To rigorously evaluate the effectiveness of the FusionGDA model, we conduct comprehensive experiments on five datasets and compare our proposed model with five competitive baseline models on the DisGeNet-Eval dataset. Notably, our case study further demonstrates the ability of FusionGDA to discover hidden associations effectively. The complete code and datasets of our experiments are available at https://github.com/ZhaohanM/FusionGDA.

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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
期刊最新文献
TUnA: an uncertainty-aware transformer model for sequence-based protein-protein interaction prediction. scLEGA: an attention-based deep clustering method with a tendency for low expression of genes on single-cell RNA-seq data. CatLearning: highly accurate gene expression prediction from histone mark. Detecting novel cell type in single-cell chromatin accessibility data via open-set domain adaptation. Explorer: efficient DNA coding by De Bruijn graph toward arbitrary local and global biochemical constraints.
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