{"title":"结果与讨论","authors":"validitas dan Reliabilitas","doi":"10.1021/acsguide.20306","DOIUrl":null,"url":null,"abstract":"prepared under the same conditions. After DNA isolation, an average amount of about 310 ng/μl DNA was obtained. All DNAs having sufficient quality and purity except one pair (n=17) were applied to Mapping Arrays. All samples, normal and tumor, achieved an overall average SNP call rate of 78.4% which was less than the 95% threshold of data quality (Table 1). CONSTRUCTION OF A WORKFLOW FOR GENOME-WIDE VARIATION ANALYSIS OF FORMALIN FIXED PARAFFIN EMBEDDED TUMOR SAMPLES","PeriodicalId":325611,"journal":{"name":"The ACS Guide to Scholarly Communication","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Results & Discussion\",\"authors\":\"validitas dan Reliabilitas\",\"doi\":\"10.1021/acsguide.20306\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"prepared under the same conditions. After DNA isolation, an average amount of about 310 ng/μl DNA was obtained. All DNAs having sufficient quality and purity except one pair (n=17) were applied to Mapping Arrays. All samples, normal and tumor, achieved an overall average SNP call rate of 78.4% which was less than the 95% threshold of data quality (Table 1). CONSTRUCTION OF A WORKFLOW FOR GENOME-WIDE VARIATION ANALYSIS OF FORMALIN FIXED PARAFFIN EMBEDDED TUMOR SAMPLES\",\"PeriodicalId\":325611,\"journal\":{\"name\":\"The ACS Guide to Scholarly Communication\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The ACS Guide to Scholarly Communication\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1021/acsguide.20306\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The ACS Guide to Scholarly Communication","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/acsguide.20306","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
prepared under the same conditions. After DNA isolation, an average amount of about 310 ng/μl DNA was obtained. All DNAs having sufficient quality and purity except one pair (n=17) were applied to Mapping Arrays. All samples, normal and tumor, achieved an overall average SNP call rate of 78.4% which was less than the 95% threshold of data quality (Table 1). CONSTRUCTION OF A WORKFLOW FOR GENOME-WIDE VARIATION ANALYSIS OF FORMALIN FIXED PARAFFIN EMBEDDED TUMOR SAMPLES
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