Literature DB >> 18089626

Significance levels for studies with correlated test statistics.

Jianxin Shi1, Douglas F Levinson, Alice S Whittemore.   

Abstract

When testing large numbers of null hypotheses, one needs to assess the evidence against the global null hypothesis that none of the hypotheses is false. Such evidence typically is based on the test statistic of the largest magnitude, whose statistical significance is evaluated by permuting the sample units to simulate its null distribution. Efron (2007) has noted that correlation among the test statistics can induce substantial interstudy variation in the shapes of their histograms, which may cause misleading tail counts. Here, we show that permutation-based estimates of the overall significance level also can be misleading when the test statistics are correlated. We propose that such estimates be conditioned on a simple measure of the spread of the observed histogram, and we provide a method for obtaining conditional significance levels. We justify this conditioning using the conditionality principle described by Cox and Hinkley (1974). Application of the method to gene expression data illustrates the circumstances when conditional significance levels are needed.

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Mesh:

Year:  2007        PMID: 18089626      PMCID: PMC3294319          DOI: 10.1093/biostatistics/kxm047

Source DB:  PubMed          Journal:  Biostatistics        ISSN: 1465-4644            Impact factor:   5.899


  3 in total

1.  Empirical bayes methods and false discovery rates for microarrays.

Authors:  Bradley Efron; Robert Tibshirani
Journal:  Genet Epidemiol       Date:  2002-06       Impact factor: 2.135

2.  Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies.

Authors:  Frank Dudbridge; Bobby P C Koeleman
Journal:  Am J Hum Genet       Date:  2004-07-19       Impact factor: 11.025

3.  Gene-expression profiles in hereditary breast cancer.

Authors:  I Hedenfalk; D Duggan; Y Chen; M Radmacher; M Bittner; R Simon; P Meltzer; B Gusterson; M Esteller; O P Kallioniemi; B Wilfond; A Borg; J Trent; M Raffeld; Z Yakhini; A Ben-Dor; E Dougherty; J Kononen; L Bubendorf; W Fehrle; S Pittaluga; S Gruvberger; N Loman; O Johannsson; H Olsson; G Sauter
Journal:  N Engl J Med       Date:  2001-02-22       Impact factor: 91.245

  3 in total
  3 in total

1.  Redundancy control in pathway databases (ReCiPa): an application for improving gene-set enrichment analysis in Omics studies and "Big data" biology.

Authors:  Juan C Vivar; Priscilla Pemu; Ruth McPherson; Sujoy Ghosh
Journal:  OMICS       Date:  2013-06-11

2.  Variable selection and dependency networks for genomewide data.

Authors:  Adrian Dobra
Journal:  Biostatistics       Date:  2009-06-11       Impact factor: 5.899

3.  Heading down the wrong pathway: on the influence of correlation within gene sets.

Authors:  Daniel M Gatti; William T Barry; Andrew B Nobel; Ivan Rusyn; Fred A Wright
Journal:  BMC Genomics       Date:  2010-10-18       Impact factor: 3.969

  3 in total

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