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1000 Titel
  • Estimands in epigenome-wide association studies
1000 Autor/in
  1. Kruppa, Jochen |
  2. Sieg, Miriam |
  3. Richter, Gesa |
  4. Pohrt, Anne |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-04-29
1000 Erschienen in
1000 Quellenangabe
  • 13(1):98
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13148-021-01083-9 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8086103/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!In DNA methylation analyses like epigenome-wide association studies, effects in differentially methylated CpG sites are assessed. Two kinds of outcomes can be used for statistical analysis: Beta-values and M-values. M-values follow a normal distribution and help to detect differentially methylated CpG sites. As biological effect measures, differences of M-values are more or less meaningless. Beta-values are of more interest since they can be interpreted directly as differences in percentage of DNA methylation at a given CpG site, but they have poor statistical properties. Different frameworks are proposed for reporting estimands in DNA methylation analysis, relying on Beta-values, M-values, or both.!##!Results!#!We present and discuss four possible approaches of achieving estimands in DNA methylation analysis. In addition, we present the usage of M-values or Beta-values in the context of bioinformatical pipelines, which often demand a predefined outcome. We show the dependencies between the differences in M-values to differences in Beta-values in two data simulations: a analysis with and without confounder effect. Without present confounder effects, M-values can be used for the statistical analysis and Beta-values statistics for the reporting. If confounder effects exist, we demonstrate the deviations and correct the effects by the intercept method. Finally, we demonstrate the theoretical problem on two large human genome-wide DNA methylation datasets to verify the results.!##!Conclusions!#!The usage of M-values in the analysis of DNA methylation data will produce effect estimates, which cannot be biologically interpreted. The parallel usage of Beta-value statistics ignores possible confounder effects and can therefore not be recommended. Hence, if the differences in Beta-values are the focus of the study, the intercept method is recommendable. Hyper- or hypomethylated CpG sites must then be carefully evaluated. If an exploratory analysis of possible CpG sites is the aim of the study, M-values can be used for inference.
1000 Sacherschließung
lokal DNA Methylation/genetics [MeSH]
lokal Methodology
lokal Genome-Wide Association Study/methods [MeSH]
lokal Multiple testing
lokal Epigenome/genetics [MeSH]
lokal Humans [MeSH]
lokal Estimands
lokal DNA methylation
lokal Epigenesis, Genetic/genetics [MeSH]
lokal Epigenome-wide association study (EWAS)
lokal Epigenetic Drugs and Clinical Trials
lokal Reproducible research
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0001-8376-8864|https://frl.publisso.de/adhoc/uri/U2llZywgTWlyaWFt|https://frl.publisso.de/adhoc/uri/UmljaHRlciwgR2VzYQ==|https://frl.publisso.de/adhoc/uri/UG9ocnQsIEFubmU=
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1000 Label
1000 Dateien
  1. Estimands in epigenome-wide association studies
1000 Objektart article
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1000 Erstellt am 2023-11-15T23:34:03.659+0100
1000 Erstellt von 322
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1000 Zuletzt bearbeitet 2023-11-30T22:50:02.006+0100
1000 Objekt bearb. Thu Nov 30 22:50:02 CET 2023
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1000 Oai Id
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