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  4. Distribution of the number of false discoveries in large-scale family-based association testing with application to the association between PTPN1 and hypertension and obesity
 
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Distribution of the number of false discoveries in large-scale family-based association testing with application to the association between PTPN1 and hypertension and obesity

Journal
Human Genetics
Journal Volume
129
Journal Issue
4
Pages
425-432
Date Issued
2011
Author(s)
Wang W.-C.
Hsiung C.A.
Wang L.-C.
LEE-MING CHUANG  
Quertermous T.
Chang I.-S.
DOI
10.1007/s00439-010-0936-y
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-79953833543&doi=10.1007%2fs00439-010-0936-y&partnerID=40&md5=1d1b7fc08de3a7f46d630f6159ecd64b
https://scholars.lib.ntu.edu.tw/handle/123456789/495649
Abstract
We present a model-free approach to the study of the number of false discoveries for large-scale simultaneous family-based association tests (FBATs) in which the set of discoveries is decided by applying a threshold to the test statistics. When the association between a set of markers in a candidate gene and a group of phenotypes is studied by a class of FBATs, we indicate that a joint null hypothesis distribution for these statistics can be obtained by the fundamental statistical method of conditioning on sufficient statistics for the null hypothesis. Based on the joint null distribution of these statistics, we can obtain the distribution of the number of false discoveries for the set of discoveries defined by a threshold; the size of this set is referred to as its tail count. Simulation studies are presented to demonstrate that the conditional, not the unconditional, distribution of the tail count is appropriate for the study of false discoveries. The usefulness of this approach is illustrated by re-examining the association between PTPN1 and a group of blood-pressure-related phenotypes reported by Olivier et al. (Hum Mol Genet 13:1885-1892, 2004); our results refine and reinforce this association. ? 2010 Springer-Verlag.
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[SDGs]SDG3

Other Subjects
low density lipoprotein cholesterol; protein tyrosine phosphatase 1B; algorithm; article; blood pressure; body height; cholesterol blood level; essential hypertension; family assessment; family based association test; gene frequency; genetic association; genetic model; genetic screening; genotype; human; null hypothesis; obesity; pedigree analysis; phenotype; priority journal; probability; progeny; simulation; statistical distribution; Algorithms; Computer Simulation; Family Health; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Testing; Humans; Hypertension; Obesity; Polymorphism, Single Nucleotide; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Reproducibility of Results; Sensitivity and Specificity
Type
journal article

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