{"title":"基于vapse的分析:一种用于阐明复杂疾病遗传易感性的两阶段候选基因方法","authors":"Brian G Weinshenker , Steve Sommer","doi":"10.1016/S1383-5726(00)00008-X","DOIUrl":null,"url":null,"abstract":"<div><p>The extraordinary success of linkage analysis in diseases with Mendelian inheritance<span> has not extended readily to the genetics of common complex diseases. VAPSE-based analysis is a type of candidate gene approach that represents an alternative strategy by which genetic mechanisms can be defined despite the presence of substantial genetic heterogeneity. Recent advances in mutation screening and statistical methodology have enhanced substantially the efficiency and power of this approach. The “bread and butter” of VAPSE-based analysis is genotype-to-phenotype searches in large populations with computerized medical records.</span></p></div>","PeriodicalId":100939,"journal":{"name":"Mutation Research/Mutation Research Genomics","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2001-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1383-5726(00)00008-X","citationCount":"2","resultStr":"{\"title\":\"VAPSE-based analysis: a two-phased candidate gene approach for elucidating genetic predisposition to complex disorders\",\"authors\":\"Brian G Weinshenker , Steve Sommer\",\"doi\":\"10.1016/S1383-5726(00)00008-X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The extraordinary success of linkage analysis in diseases with Mendelian inheritance<span> has not extended readily to the genetics of common complex diseases. VAPSE-based analysis is a type of candidate gene approach that represents an alternative strategy by which genetic mechanisms can be defined despite the presence of substantial genetic heterogeneity. Recent advances in mutation screening and statistical methodology have enhanced substantially the efficiency and power of this approach. The “bread and butter” of VAPSE-based analysis is genotype-to-phenotype searches in large populations with computerized medical records.</span></p></div>\",\"PeriodicalId\":100939,\"journal\":{\"name\":\"Mutation Research/Mutation Research Genomics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1383-5726(00)00008-X\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mutation Research/Mutation Research Genomics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S138357260000008X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mutation Research/Mutation Research Genomics","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S138357260000008X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
VAPSE-based analysis: a two-phased candidate gene approach for elucidating genetic predisposition to complex disorders
The extraordinary success of linkage analysis in diseases with Mendelian inheritance has not extended readily to the genetics of common complex diseases. VAPSE-based analysis is a type of candidate gene approach that represents an alternative strategy by which genetic mechanisms can be defined despite the presence of substantial genetic heterogeneity. Recent advances in mutation screening and statistical methodology have enhanced substantially the efficiency and power of this approach. The “bread and butter” of VAPSE-based analysis is genotype-to-phenotype searches in large populations with computerized medical records.