True and false positive peaks in genomewide scans: Applications of length-biased sampling to linkage mapping

被引:122
作者
Terwilliger, JD
Shannon, WD
Lathrop, GM
Nolan, JP
Goldin, LR
Chase, GA
Weeks, DE
机构
[1] UNIV OXFORD, WELLCOME TRUST CTR HUMAN GENET, OXFORD OX3 7BN, ENGLAND
[2] COLUMBIA UNIV, DEPT PSYCHIAT, NEW YORK, NY USA
[3] COLUMBIA UNIV, COLUMBIA GENOME CTR, NEW YORK, NY USA
[4] UNIV WASHINGTON, SCH MED, ST LOUIS, MO USA
[5] AMERICAN UNIV, DEPT MATH & STAT, WASHINGTON, DC 20016 USA
[6] NATL CTR HLTH STAT, NATL INST HLTH, HYATTSVILLE, MD USA
[7] GEORGETOWN UNIV, MED CTR, WASHINGTON, DC 20007 USA
[8] NIMH, CLIN NEUROGENET BRANCH, BETHESDA, MD 20892 USA
[9] UNIV PITTSBURGH, DEPT HUMAN GENET, PITTSBURGH, PA USA
基金
英国惠康基金;
关键词
D O I
10.1086/514855
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Disease-susceptibility Loci are now being mapped via genomewide scans in which a linkage statistic is computed at each of a large number of markers, Such disease-susceptibility loci may be identified via a peak in the test statistic when the latter is plotted against the genetic map, In this paper we establish, by appealing to renewal theory, that true positive peaks are expected to be longer than false positive peaks, These results are verified by a realistic simulation of a genomewide linkage study based on the affected-sib-pair design, Since longer peaks are more likely to contain a gene of interest than are shorter peaks, these differences may aid in linkage mapping, justifying assignment of lower priority to shorter peaks, However, since these differences are generally small, statistics based on both peak length and height may not be much more powerful than those based on height alone, The results presented here also provide a theoretical framework for methods that use the length of shared haplotypes in populations to map disease genes.
引用
收藏
页码:430 / 438
页数:9
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