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PMID: 15956674 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Quantitative trait Loci analysis using the false discovery rate.

Genetics ·Vol. 171 ·No. 2 ·2005-10-00 ·Pages 783-90

Benjamini Y, Yekutieli D

Abstract

False discovery rate control has become an essential tool in any study that has a very large multiplicity problem. False discovery rate-controlling procedures have also been found to be very effective in QTL analysis, ensuring reproducible results with few falsely discovered linkages and offering increased power to discover QTL, although their acceptance has been slower than in microarray analysis, for example. The reason is partly because the methodological aspects of applying the false discovery rate to QTL mapping are not well developed. Our aim in this work is to lay a solid foundation for the use of the false discovery rate in QTL mapping. We review the false discovery rate criterion, the appropriate interpretation of the FDR, and alternative formulations of the FDR that appeared in the statistical and genetics literature. We discuss important features of the FDR approach, some stemming from new developments in FDR theory and methodology, which deem it especially useful in linkage analysis. We review false discovery rate-controlling procedures--the BH, the resampling procedure, and the adaptive two-stage procedure-and discuss the validity of these procedures in single- and multiple-trait QTL mapping. Finally we argue that the control of the false discovery rate has an important role in suggesting, indicating the significance of, and confirming QTL and present guidelines for its use.

MeSH Terms
Chromosome Mapping/methods Computer Simulation Models, Genetic Quantitative Trait Loci Research Design
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Benjamini Yoav
Department of Statistics and Operations Research, Tel Aviv University, Israel.
Yekutieli Daniel
References (8)
8 references, click to expand
  1. Using the false discovery rate approach in the genetic dissection of complex traits: a response to Weller et al.
    Genetics. 2000 Apr;154(4):1917-8 PMID: 10950641
  2. A whole genome scan for quantitative trait loci affecting milk protein percentage in Israeli-Holstein cattle, by means of selective milk DNA pooling in a daughter design, using an adjusted false discovery rate criterion.
    Genetics. 2001 Apr;157(4):1683-98 PMID: 11290723
  3. Application of the false discovery rate to quantitative trait loci interval mapping with multiple traits.
    Genetics. 2002 Jun;161(2):905-14 PMID: 12072484
  4. A new approach to the problem of multiple comparisons in the genetic dissection of complex traits.
    Genetics. 1998 Dec;150(4):1699-706 PMID: 9832544
  5. Controlling the proportion of false positives in multiple dependent tests.
    Genetics. 2004 Jan;166(1):611-9 PMID: 15020448
  6. Empirical threshold values for quantitative trait mapping.
    Genetics. 1994 Nov;138(3):963-71 PMID: 7851788
  7. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results.
    Nat Genet. 1995 Nov;11(3):241-7 PMID: 7581446
  8. False discovery rate in linkage and association genome screens for complex disorders.
    Genetics. 2003 Jun;164(2):829-33 PMID: 12807801
Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
2005-10-00
Epub
2005-00-14
Pages
783-90
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1456787
Subset
IM
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