Guangyao Chen, James Sargant, S. Houghten, T. K. Collins
{"title":"利用进化计算鉴定与阿尔茨海默病相关的基因","authors":"Guangyao Chen, James Sargant, S. Houghten, T. K. Collins","doi":"10.1109/CIBCB49929.2021.9562876","DOIUrl":null,"url":null,"abstract":"A multi-objective genetic algorithm is applied to the problem of identifying genes associated with Alzheimer's disease. The input to the genetic algorithm is a set of centrality measures obtained by merging various biological evidence types into a complex network, based on a set of 11 genes already known to be associated with this disease. In terms of leave-one-out validation, the strongest results are obtained using betweenness, with ranking showing that better results are sometimes obtained by including either stress or load with betweenness. The overall ranking of the genes across all runs is examined and suggests some genes worthy of further study with respect to their link to this disease. The methodology is also evaluated with respect to robustness by modifying the original network by a range of percentages, and applying the methodology to these variations. The results show that the methodology returns very similar results under these circumstances.","PeriodicalId":163387,"journal":{"name":"2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology (CIBCB)","volume":"67 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Identification of Genes Associated with Alzheimer's Disease using Evolutionary Computation\",\"authors\":\"Guangyao Chen, James Sargant, S. Houghten, T. K. Collins\",\"doi\":\"10.1109/CIBCB49929.2021.9562876\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A multi-objective genetic algorithm is applied to the problem of identifying genes associated with Alzheimer's disease. The input to the genetic algorithm is a set of centrality measures obtained by merging various biological evidence types into a complex network, based on a set of 11 genes already known to be associated with this disease. In terms of leave-one-out validation, the strongest results are obtained using betweenness, with ranking showing that better results are sometimes obtained by including either stress or load with betweenness. The overall ranking of the genes across all runs is examined and suggests some genes worthy of further study with respect to their link to this disease. The methodology is also evaluated with respect to robustness by modifying the original network by a range of percentages, and applying the methodology to these variations. The results show that the methodology returns very similar results under these circumstances.\",\"PeriodicalId\":163387,\"journal\":{\"name\":\"2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology (CIBCB)\",\"volume\":\"67 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology (CIBCB)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/CIBCB49929.2021.9562876\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology (CIBCB)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/CIBCB49929.2021.9562876","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Identification of Genes Associated with Alzheimer's Disease using Evolutionary Computation
A multi-objective genetic algorithm is applied to the problem of identifying genes associated with Alzheimer's disease. The input to the genetic algorithm is a set of centrality measures obtained by merging various biological evidence types into a complex network, based on a set of 11 genes already known to be associated with this disease. In terms of leave-one-out validation, the strongest results are obtained using betweenness, with ranking showing that better results are sometimes obtained by including either stress or load with betweenness. The overall ranking of the genes across all runs is examined and suggests some genes worthy of further study with respect to their link to this disease. The methodology is also evaluated with respect to robustness by modifying the original network by a range of percentages, and applying the methodology to these variations. The results show that the methodology returns very similar results under these circumstances.