Literature DB >> 21427757

A novel approach for small sample size family-based association studies: sequential tests.

Ozlem Ilk1, Farid Rajabli, Dilay Ciglidag Dungul, Hilal Ozdag, Hakki Gokhan Ilk.   

Abstract

In this paper, we propose a sequential probability ratio test (SPRT) to overcome the problem of limited samples in studies related to complex genetic diseases. The results of this novel approach are compared with the ones obtained from the traditional transmission disequilibrium test (TDT) on simulated data. Although TDT classifies single-nucleotide polymorphisms (SNPs) to only two groups (SNPs associated with the disease and the others), SPRT has the flexibility of assigning SNPs to a third group, that is, those for which we do not have enough evidence and should keep sampling. It is shown that SPRT results in smaller ratios of false positives and negatives, as well as better accuracy and sensitivity values for classifying SNPs when compared with TDT. By using SPRT, data with small sample size become usable for an accurate association analysis.

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Year:  2011        PMID: 21427757      PMCID: PMC3172932          DOI: 10.1038/ejhg.2011.51

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  11 in total

Review 1.  Family-based tests of association and/or linkage.

Authors:  J C Whittaker; A P Morris
Journal:  Ann Hum Genet       Date:  2001-09       Impact factor: 1.670

2.  A general and accurate approach for computing the statistical power of the transmission disequilibrium test for complex disease genes.

Authors:  W M Chen; H W Deng
Journal:  Genet Epidemiol       Date:  2001-07       Impact factor: 2.135

3.  Exact unconditional tests for a 2 x 2 matched-pairs design.

Authors:  R L Berger; K Sidik
Journal:  Stat Methods Med Res       Date:  2003-03       Impact factor: 3.021

4.  Early stopping in clinical trials and epidemiologic studies for "futility": conditional power versus sequential analysis.

Authors:  Ingeborg van der Tweel; Paulus A H van Noord
Journal:  J Clin Epidemiol       Date:  2003-07       Impact factor: 6.437

5.  Genetic association studies.

Authors:  Heather J Cordell; David G Clayton
Journal:  Lancet       Date:  2005 Sep 24-30       Impact factor: 79.321

Review 6.  The road to genome-wide association studies.

Authors:  Leonid Kruglyak
Journal:  Nat Rev Genet       Date:  2008-02-19       Impact factor: 53.242

7.  Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

Authors:  R S Spielman; R E McGinnis; W J Ewens
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

Review 8.  Efficient ways exist to obtain the optimal sample size in clinical trials in rare diseases.

Authors:  J H van der Lee; J Wesseling; M W T Tanck; M Offringa
Journal:  J Clin Epidemiol       Date:  2008-02-21       Impact factor: 6.437

9.  Sample size computation for association studies using case-parents design.

Authors:  Najla Kharrat; Imen Ayadi; Ahmed Rebaï
Journal:  J Genet       Date:  2006-12       Impact factor: 1.508

10.  Family-based versus unrelated case-control designs for genetic associations.

Authors:  Evangelos Evangelou; Thomas A Trikalinos; Georgia Salanti; John P A Ioannidis
Journal:  PLoS Genet       Date:  2006-06-26       Impact factor: 5.917

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  1 in total

1.  Power analysis of C-TDT for small sample size genome-wide association studies by the joint use of case-parent trios and pairs.

Authors:  Farid Rajabli; Gul Inan; Ozlem Ilk
Journal:  Comput Math Methods Med       Date:  2013-05-02       Impact factor: 2.238

  1 in total

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