{"title":"数量","authors":"B. Gillham","doi":"10.4324/9780429503733-3","DOIUrl":null,"url":null,"abstract":"CNVs are structural genetic variations. Their detection is currently a heavily discussed problem in the area of bioinformatics, in part due to their proved (positive or negative) association with diseases like cancer, AIDS and neuropsychiatric disorders. In this text, we will study several approaches and their applicability, in order to obtain an insight into the challenges presented and how they are confronted.","PeriodicalId":197308,"journal":{"name":"A Grammar of Mursi","volume":"10 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"345","resultStr":"{\"title\":\"Number\",\"authors\":\"B. Gillham\",\"doi\":\"10.4324/9780429503733-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"CNVs are structural genetic variations. Their detection is currently a heavily discussed problem in the area of bioinformatics, in part due to their proved (positive or negative) association with diseases like cancer, AIDS and neuropsychiatric disorders. In this text, we will study several approaches and their applicability, in order to obtain an insight into the challenges presented and how they are confronted.\",\"PeriodicalId\":197308,\"journal\":{\"name\":\"A Grammar of Mursi\",\"volume\":\"10 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-09-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"345\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"A Grammar of Mursi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4324/9780429503733-3\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"A Grammar of Mursi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4324/9780429503733-3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
CNVs are structural genetic variations. Their detection is currently a heavily discussed problem in the area of bioinformatics, in part due to their proved (positive or negative) association with diseases like cancer, AIDS and neuropsychiatric disorders. In this text, we will study several approaches and their applicability, in order to obtain an insight into the challenges presented and how they are confronted.
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