{"title":"Inter-session reproducibility measures for high-throughput data sources.","authors":"Milos Hauskrecht, Richard Pelikan","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>High-throughput biological assays such as micro-arrays and mass spectrometry (MS) have risen as potential clinical tools for disease detection. Multiple potential biomarkers can be rapidly and cheaply evaluated for a large number of patients. Typical research and evaluation studies in these fields have focused primarily on data that were generated from samples in a single data-generation session. However, in the clinical setting, new patients screened by the technology will arrive at different times and data will unavoidably come from multiple data-generation sessions. The understanding and assessment of multi-session effects on data generated by the technology is critical for its application to clinical practice. This paper proposes a methodology for measuring and testing the reproducibility of various aspects of high-throughput data across multiple data-generation sessions. We test and demonstrate the framework on mass-spectrometry data obtained from four different data-generation sessions for the same set of samples.</p>","PeriodicalId":89276,"journal":{"name":"Summit on translational bioinformatics","volume":"2008 ","pages":"41-5"},"PeriodicalIF":0.0000,"publicationDate":"2008-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3041518/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Summit on translational bioinformatics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
High-throughput biological assays such as micro-arrays and mass spectrometry (MS) have risen as potential clinical tools for disease detection. Multiple potential biomarkers can be rapidly and cheaply evaluated for a large number of patients. Typical research and evaluation studies in these fields have focused primarily on data that were generated from samples in a single data-generation session. However, in the clinical setting, new patients screened by the technology will arrive at different times and data will unavoidably come from multiple data-generation sessions. The understanding and assessment of multi-session effects on data generated by the technology is critical for its application to clinical practice. This paper proposes a methodology for measuring and testing the reproducibility of various aspects of high-throughput data across multiple data-generation sessions. We test and demonstrate the framework on mass-spectrometry data obtained from four different data-generation sessions for the same set of samples.