{"title":"微阵列数据分析的不完全显性遗传算法","authors":"N. T. Melita, S. Holban","doi":"10.1109/ICCP.2016.7737137","DOIUrl":null,"url":null,"abstract":"We address the problem of analyzing the vast amount of data involved in microarray studies. The finality is to discover, from a large pool of candidates, a limited number of genes that could be causally related with a specific pathology. In this context, we propose a new genetic algorithm (GA) approach for feature selection, with diploid number of chromosomes and an incomplete dominance model for genotype to phenotype mapping. We test our algorithm on a familiar data set for performance evaluation purposes.","PeriodicalId":343658,"journal":{"name":"2016 IEEE 12th International Conference on Intelligent Computer Communication and Processing (ICCP)","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"An incomplete dominance genetic algorithm approach to microarray data analysis\",\"authors\":\"N. T. Melita, S. Holban\",\"doi\":\"10.1109/ICCP.2016.7737137\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We address the problem of analyzing the vast amount of data involved in microarray studies. The finality is to discover, from a large pool of candidates, a limited number of genes that could be causally related with a specific pathology. In this context, we propose a new genetic algorithm (GA) approach for feature selection, with diploid number of chromosomes and an incomplete dominance model for genotype to phenotype mapping. We test our algorithm on a familiar data set for performance evaluation purposes.\",\"PeriodicalId\":343658,\"journal\":{\"name\":\"2016 IEEE 12th International Conference on Intelligent Computer Communication and Processing (ICCP)\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2016 IEEE 12th International Conference on Intelligent Computer Communication and Processing (ICCP)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ICCP.2016.7737137\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2016 IEEE 12th International Conference on Intelligent Computer Communication and Processing (ICCP)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICCP.2016.7737137","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
An incomplete dominance genetic algorithm approach to microarray data analysis
We address the problem of analyzing the vast amount of data involved in microarray studies. The finality is to discover, from a large pool of candidates, a limited number of genes that could be causally related with a specific pathology. In this context, we propose a new genetic algorithm (GA) approach for feature selection, with diploid number of chromosomes and an incomplete dominance model for genotype to phenotype mapping. We test our algorithm on a familiar data set for performance evaluation purposes.