Evidence map›Paper›PMID 27258058›Full record

ArticlePloS one2016

A Comparative Study of Five Association Tests Based on CpG Set for Epigenome-Wide Association Studies.

Qiuyi Zhang, Yang Zhao, Ruyang Zhang, Yongyue Wei, Honggang Yi, Fang Shao, Feng Chen

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Machine Learning in Epigenomics: Insights into Cancer Biology and Medicine.Biochimica et biophysica acta. Reviews on cancer · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Qiuyi ZhangDepartment of Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, China, 211166.
Yang ZhaoDepartment of Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, China, 211166.
Ruyang ZhangDepartment of Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, China, 211166.
Yongyue WeiDepartment of Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, China, 211166.
Honggang YiDepartment of Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, China, 211166.
Fang ShaoDepartment of Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, China, 211166.
Feng ChenDepartment of Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, China, 211166.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An epigenome-wide association study (EWAS) is a large-scale study of human disease-associated epigenetic variation, specifically variation in DNA methylation. High throughput technologies enable simultaneous epigenetic profiling of DNA methylation at hundreds of thousands of CpGs across the genome. The clustering of correlated DNA methylation at CpGs is reportedly similar to that of linkage-disequilibrium (LD) correlation in genetic single nucleotide polymorphisms (SNP) variation. However, current analysis methods, such as the t-test and rank-sum test, may be underpowered to detect differentially methylated markers. We propose to test the association between the outcome (e.g case or control) and a set of CpG sites jointly. Here, we compared the performance of five CpG set analysis approaches: principal component analysis (PCA), supervised principal component analysis (SPCA), kernel principal component analysis (KPCA), sequence kernel association test (SKAT), and sliced inverse regression (SIR) with Hotelling's T2 test and t-test using Bonferroni correction. The simulation results revealed that the first six methods can control the type I error at the significance level, while the t-test is conservative. SPCA and SKAT performed better than other approaches when the correlation among CpG sites was strong. For illustration, these methods were also applied to a real methylation dataset.

Indexed as

CpG IslandsDNA MethylationEpigenesis, GeneticEpigenomicsGenome-Wide Association StudyHumansLinkage DisequilibriumPrincipal Component Analysis

Identifiers

PMID27258058
PMCPMC4892473

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.