{"title":"On clone assembly problems: an error-tolerant test for interval graphs","authors":"W. Hsu, Wei-Fu Lu","doi":"10.1109/IJSIS.1998.685428","DOIUrl":null,"url":null,"abstract":"An important problem in DNA physical mapping is to reassemble the clone fragments to determine the structure of the entire molecule. The error-free version of this problem can be modeled as an interval graph recognition problem, where an interval graph is the intersection graph of a collection of intervals. However, since the data collected from laboratories almost surely contain some errors, traditional recognition algorithms can hardly be applied directly. We present a new test which has the following features: 1) the algorithm assembles the clones efficiently when the data is error-free; 2) in a case when the error rate is small (say, less than 3%) the test can likely detect and automatically correct the following three types of errors false positives, false negatives and chimeric clones; and 3) the test also identifies those parts of the data that are problematic, thus allowing biologists to perform further experiments to clean up the data.","PeriodicalId":289764,"journal":{"name":"Proceedings. IEEE International Joint Symposia on Intelligence and Systems (Cat. No.98EX174)","volume":"34 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1998-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings. IEEE International Joint Symposia on Intelligence and Systems (Cat. No.98EX174)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/IJSIS.1998.685428","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
An important problem in DNA physical mapping is to reassemble the clone fragments to determine the structure of the entire molecule. The error-free version of this problem can be modeled as an interval graph recognition problem, where an interval graph is the intersection graph of a collection of intervals. However, since the data collected from laboratories almost surely contain some errors, traditional recognition algorithms can hardly be applied directly. We present a new test which has the following features: 1) the algorithm assembles the clones efficiently when the data is error-free; 2) in a case when the error rate is small (say, less than 3%) the test can likely detect and automatically correct the following three types of errors false positives, false negatives and chimeric clones; and 3) the test also identifies those parts of the data that are problematic, thus allowing biologists to perform further experiments to clean up the data.