{"title":"6. 稀疏抽样曲线的统计","authors":"M. Holden, L. Holden","doi":"10.18261/9788215041193-2020-06","DOIUrl":null,"url":null,"abstract":"We develop new statistical methods for analyzing sparsely sampled curves that vary in time. The typical dataset is differences in log gene expressions from case-control pairs for a large number of genes sampled relative to time of diagnosis. We focus on weak signals in the gene expression in many genes instead of strong signals in a few genes. The methods are based on moving windows in time, hypothesis testing, dimension reductions and randomization of the time to observa-tion.","PeriodicalId":386489,"journal":{"name":"Advancing Systems Epidemiology in Cancer","volume":"107 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"6. Statistics of Sparsely Sampled Curves\",\"authors\":\"M. Holden, L. Holden\",\"doi\":\"10.18261/9788215041193-2020-06\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We develop new statistical methods for analyzing sparsely sampled curves that vary in time. The typical dataset is differences in log gene expressions from case-control pairs for a large number of genes sampled relative to time of diagnosis. We focus on weak signals in the gene expression in many genes instead of strong signals in a few genes. The methods are based on moving windows in time, hypothesis testing, dimension reductions and randomization of the time to observa-tion.\",\"PeriodicalId\":386489,\"journal\":{\"name\":\"Advancing Systems Epidemiology in Cancer\",\"volume\":\"107 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-12-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advancing Systems Epidemiology in Cancer\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18261/9788215041193-2020-06\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advancing Systems Epidemiology in Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18261/9788215041193-2020-06","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
We develop new statistical methods for analyzing sparsely sampled curves that vary in time. The typical dataset is differences in log gene expressions from case-control pairs for a large number of genes sampled relative to time of diagnosis. We focus on weak signals in the gene expression in many genes instead of strong signals in a few genes. The methods are based on moving windows in time, hypothesis testing, dimension reductions and randomization of the time to observa-tion.