{"title":"决策树分类器在新一代测序数据单核苷酸多态性发现中的应用","authors":"Muhammad Abrar Istiadi, W. Kusuma, I Made Tasma","doi":"10.1109/ICACSIS.2014.7065832","DOIUrl":null,"url":null,"abstract":"Single Nucleotide Polymorphism (SNP) is the most abundant form of genetic variation and proven to be advantageous in diverse genetic-related studies. However, accurate determination of true SNPs from next-generation sequencing (NGS) data is a challenging task due to high error rates of NGS. To overcome this problem, we applied a machine learning method using C4.5 decision tree algorithm to discover SNPs from whole-genome NGS data. In addition, we conducted random undersampling to deal with the imbalanced data. The result shows that the proposed method is able to identify most of the true SNPs with more than 90% recall, but still suffers from a high rate of false-positives.","PeriodicalId":443250,"journal":{"name":"2014 International Conference on Advanced Computer Science and Information System","volume":"84 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2014-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Application of decision tree classifier for single nucleotide polymorphism discovery from next-generation sequencing data\",\"authors\":\"Muhammad Abrar Istiadi, W. Kusuma, I Made Tasma\",\"doi\":\"10.1109/ICACSIS.2014.7065832\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Single Nucleotide Polymorphism (SNP) is the most abundant form of genetic variation and proven to be advantageous in diverse genetic-related studies. However, accurate determination of true SNPs from next-generation sequencing (NGS) data is a challenging task due to high error rates of NGS. To overcome this problem, we applied a machine learning method using C4.5 decision tree algorithm to discover SNPs from whole-genome NGS data. In addition, we conducted random undersampling to deal with the imbalanced data. The result shows that the proposed method is able to identify most of the true SNPs with more than 90% recall, but still suffers from a high rate of false-positives.\",\"PeriodicalId\":443250,\"journal\":{\"name\":\"2014 International Conference on Advanced Computer Science and Information System\",\"volume\":\"84 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2014 International Conference on Advanced Computer Science and Information System\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/ICACSIS.2014.7065832\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2014 International Conference on Advanced Computer Science and Information System","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/ICACSIS.2014.7065832","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Application of decision tree classifier for single nucleotide polymorphism discovery from next-generation sequencing data
Single Nucleotide Polymorphism (SNP) is the most abundant form of genetic variation and proven to be advantageous in diverse genetic-related studies. However, accurate determination of true SNPs from next-generation sequencing (NGS) data is a challenging task due to high error rates of NGS. To overcome this problem, we applied a machine learning method using C4.5 decision tree algorithm to discover SNPs from whole-genome NGS data. In addition, we conducted random undersampling to deal with the imbalanced data. The result shows that the proposed method is able to identify most of the true SNPs with more than 90% recall, but still suffers from a high rate of false-positives.