Evidence map›Paper›PMID 29776330›Full record

ArticleBMC bioinformatics2018

Robust joint score tests in the application of DNA methylation data analysis.

Xuan Li, Yuejiao Fu, Xiaogang Wang, Weiliang Qiu

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Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xuan LiDepartment of Mathematics and Statistics, York University, 4700 Keele Street, Toronto, M3J1P3, Canada.
Yuejiao FuDepartment of Mathematics and Statistics, York University, 4700 Keele Street, Toronto, M3J1P3, Canada. yuejiao@mathstat.yorku.ca.ORCID 0000-0001-8606-570X
Xiaogang WangDepartment of Mathematics and Statistics, York University, 4700 Keele Street, Toronto, M3J1P3, Canada.
Weiliang QiuChanning Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, 181 Longwood Avenue, Boston, 02115, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecently differential variability has been showed to be valuable in evaluating the association of DNA methylation to the risks of complex human diseases. The statistical tests based on both differential methylation level and differential variability can be more powerful than those based only on differential methylation level. Anh and Wang (2013) proposed a joint score test (AW) to simultaneously detect for differential methylation and differential variability. However, AW's method seems to be quite conservative and has not been fully compared with existing joint tests.

resultsWe proposed three improved joint score tests, namely iAW.Lev, iAW.BF, and iAW.TM, and have made extensive comparisons with the joint likelihood ratio test (jointLRT), the Kolmogorov-Smirnov (KS) test, and the AW test. Systematic simulation studies showed that: 1) the three improved tests performed better (i.e., having larger power, while keeping nominal Type I error rates) than the other three tests for data with outliers and having different variances between cases and controls; 2) for data from normal distributions, the three improved tests had slightly lower power than jointLRT and AW. The analyses of two Illumina HumanMethylation27 data sets GSE37020 and GSE20080 and one Illumina Infinium MethylationEPIC data set GSE107080 demonstrated that three improved tests had higher true validation rates than those from jointLRT, KS, and AW.

conclusionsThe three proposed joint score tests are robust against the violation of normality assumption and presence of outlying observations in comparison with other three existing tests. Among the three proposed tests, iAW.BF seems to be the most robust and effective one for all simulated scenarios and also in real data analyses.

Indexed as

AlgorithmsData AnalysisComputer SimulationDiseaseDNA MethylationHumansStatistics, NonparametricJoint score testsMethylation dataVariability

Identifiers

PMID29776330
PMCPMC5960098

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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.