MLW-BFECF: a multi-weighted dynamic cascade forest based on bilinear feature extraction for predicting the stage of Kidney Renal Clear Cell Carcinoma on multi-modal gene data.
{"title":"MLW-BFECF: a multi-weighted dynamic cascade forest based on bilinear feature extraction for predicting the stage of Kidney Renal Clear Cell Carcinoma on multi-modal gene data.","authors":"Liye Jia, Liancheng Jiang, Junhong Yue, Fang Hao, Yongfei Wu, Xilin Liu","doi":"10.1109/TCBB.2024.3486742","DOIUrl":null,"url":null,"abstract":"<p><p>The stage prediction of kidney renal clear cell carcinoma (KIRC) is important for the diagnosis, personalized treatment, and prognosis of patients. Many prediction methods have been proposed, but most of them are based on unimodal gene data, and their accuracy is difficult to further improve. Therefore, we propose a novel multi-weighted dynamic cascade forest based on the bilinear feature extraction (MLW-BFECF) model for stage prediction of KIRC using multimodal gene datasets (RNA-seq, CNA, and methylation). The proposed model utilizes a dynamic cascade framework with shuffle layers to prevent early degradation of the model. In each cascade layer, a voting technique based on three gene selection algorithms is first employed to effectively retain gene features more relevant to KIRC and eliminate redundant information in gene features. Then, two new bilinear models based on the gated attention mechanism are proposed to better extract new intra-modal and inter-modal gene features; Finally, based on the idea of the bagging, a multi-weighted ensemble forest classifiers module is proposed to extract and fuse probabilistic features of the three-modal gene data. A series of experiments demonstrate that the MLW-BFECF model based on the three-modal KIRC dataset achieves the highest prediction performance with an accuracy of 88.92%.</p>","PeriodicalId":13344,"journal":{"name":"IEEE/ACM Transactions on Computational Biology and Bioinformatics","volume":null,"pages":null},"PeriodicalIF":3.6000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE/ACM Transactions on Computational Biology and Bioinformatics","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1109/TCBB.2024.3486742","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
The stage prediction of kidney renal clear cell carcinoma (KIRC) is important for the diagnosis, personalized treatment, and prognosis of patients. Many prediction methods have been proposed, but most of them are based on unimodal gene data, and their accuracy is difficult to further improve. Therefore, we propose a novel multi-weighted dynamic cascade forest based on the bilinear feature extraction (MLW-BFECF) model for stage prediction of KIRC using multimodal gene datasets (RNA-seq, CNA, and methylation). The proposed model utilizes a dynamic cascade framework with shuffle layers to prevent early degradation of the model. In each cascade layer, a voting technique based on three gene selection algorithms is first employed to effectively retain gene features more relevant to KIRC and eliminate redundant information in gene features. Then, two new bilinear models based on the gated attention mechanism are proposed to better extract new intra-modal and inter-modal gene features; Finally, based on the idea of the bagging, a multi-weighted ensemble forest classifiers module is proposed to extract and fuse probabilistic features of the three-modal gene data. A series of experiments demonstrate that the MLW-BFECF model based on the three-modal KIRC dataset achieves the highest prediction performance with an accuracy of 88.92%.
期刊介绍:
IEEE/ACM Transactions on Computational Biology and Bioinformatics emphasizes the algorithmic, mathematical, statistical and computational methods that are central in bioinformatics and computational biology; the development and testing of effective computer programs in bioinformatics; the development of biological databases; and important biological results that are obtained from the use of these methods, programs and databases; the emerging field of Systems Biology, where many forms of data are used to create a computer-based model of a complex biological system