Meta-analysis of genetic association studies

Meta-analysis, a statistical tool for combining results across studies, is becoming popular as a method for resolving discrepancies in genetic association studies. Persistent difficulties in obtaining robust, replicable results in genetic association studies are almost certainly because genetic effe...

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Published inTrends in genetics Vol. 20; no. 9; pp. 439 - 444
Main Authors Munafò, Marcus R., Flint, Jonathan
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.09.2004
Elsevier Science
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Abstract Meta-analysis, a statistical tool for combining results across studies, is becoming popular as a method for resolving discrepancies in genetic association studies. Persistent difficulties in obtaining robust, replicable results in genetic association studies are almost certainly because genetic effects are small, requiring studies with many thousands of subjects to be detected. In this article, we describe how meta-analysis works and consider whether it will solve the problem of underpowered studies or whether it is another affliction visited by statisticians on geneticists. We show that meta-analysis has been successful in revealing unexpected sources of heterogeneity, such as publication bias. If heterogeneity is adequately recognized and taken into account, meta-analysis can confirm the involvement of a genetic variant, but it is not a substitute for an adequately powered primary study.
AbstractList Meta-analysis, a statistical tool for combining results across studies, is becoming popular as a method for resolving discrepancies in genetic association studies. Persistent difficulties in obtaining robust, replicable results in genetic association studies are almost certainly because genetic effects are small, requiring studies with many thousands of subjects to be detected. In this article, we describe how meta-analysis works and consider whether it will solve the problem of underpowered studies or whether it is another affliction visited by statisticians on geneticists. We show that meta-analysis has been successful in revealing unexpected sources of heterogeneity, such as publication bias. If heterogeneity is adequately recognized and taken into account, meta-analysis can confirm the involvement of a genetic variant, but it is not a substitute for an adequately powered primary study.
Meta-analysis, a statistical tool for combining results across studies, is becoming popular as a method for resolving discrepancies in genetic association studies. Persistent difficulties in obtaining robust, replicable results in genetic association studies are almost certainly because genetic effects are small, requiring studies with many thousands of subjects to be detected. In this article, we describe how meta-analysis works and consider whether it will solve the problem of underpowered studies or whether it is another affliction visited by statisticians on geneticists. We show that meta-analysis has been successful in revealing unexpected sources of heterogeneity, such as publication bias. If heterogeneity is adequately recognized and taken into account, meta-analysis can confirm the involvement of a genetic variant, but it is not a substitute for an adequately powered primary study.Meta-analysis, a statistical tool for combining results across studies, is becoming popular as a method for resolving discrepancies in genetic association studies. Persistent difficulties in obtaining robust, replicable results in genetic association studies are almost certainly because genetic effects are small, requiring studies with many thousands of subjects to be detected. In this article, we describe how meta-analysis works and consider whether it will solve the problem of underpowered studies or whether it is another affliction visited by statisticians on geneticists. We show that meta-analysis has been successful in revealing unexpected sources of heterogeneity, such as publication bias. If heterogeneity is adequately recognized and taken into account, meta-analysis can confirm the involvement of a genetic variant, but it is not a substitute for an adequately powered primary study.
Author Munafò, Marcus R.
Flint, Jonathan
Author_xml – sequence: 1
  givenname: Marcus R.
  surname: Munafò
  fullname: Munafò, Marcus R.
  email: marcus.munafo@clinpharm.ox.ac.uk
– sequence: 2
  givenname: Jonathan
  surname: Flint
  fullname: Flint, Jonathan
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SubjectTerms Animals
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Genes - genetics
Genetic Techniques
Genetics
Genetics of eukaryotes. Biological and molecular evolution
Models, Genetic
Molecular and cellular biology
Multivariate Analysis
Personality - genetics
Title Meta-analysis of genetic association studies
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0168952504001799
https://dx.doi.org/10.1016/j.tig.2004.06.014
https://www.ncbi.nlm.nih.gov/pubmed/15313553
https://www.proquest.com/docview/17704758
https://www.proquest.com/docview/66792204
Volume 20
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