Evidence map›Paper›PMID 38967555›Full record

ArticleEpigenetics2024

Direction-aware functional class scoring enrichment analysis of infinium DNA methylation data.

Mark Ziemann, Mandhri Abeysooriya, Anusuiya Bora, Séverine Lamon, Mary Sravya Kasu, Mitchell W Norris, Yen Ting Wong, Jeffrey M Craig

Abstract read
In one paragraph

Article in Epigenetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Mark ZiemannBioinformatics Working Group, Burnet Institute, Melbourne, Australia.ORCID 0000-0002-7688-6974
Mandhri AbeysooriyaSchool of Life and Environmental Sciences, Deakin University, Geelong, Australia.ORCID 0000-0003-2163-6203
Anusuiya BoraBioinformatics Working Group, Burnet Institute, Melbourne, Australia.ORCID 0009-0006-2908-1352
Séverine LamonSchool of Exercise and Nutrition Sciences, Institute for Physical Activity and Nutrition, Deakin University, Geelong, Australia.ORCID 0000-0002-3271-6551
Mary Sravya KasuSchool of Life and Environmental Sciences, Deakin University, Geelong, Australia.ORCID 0000-0002-7891-836X
Mitchell W NorrisSchool of Life and Environmental Sciences, Deakin University, Geelong, Australia.ORCID 0009-0001-4338-6252
Yen Ting WongSchool of Medicine, Deakin University, Geelong, Australia.ORCID 0000-0003-3120-0964
Jeffrey M CraigSchool of Medicine, Deakin University, Geelong, Australia.ORCID 0000-0003-3979-7849

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infinium Methylation BeadChip arrays remain one of the most popular platforms for epigenome-wide association studies, but tools for downstream pathway analysis have their limitations. Functional class scoring (FCS) is a group of pathway enrichment techniques that involve the ranking of genes and evaluation of their collective regulation in biological systems, but the implementations described for Infinium methylation array data do not retain direction information, which is important for mechanistic understanding of genomic regulation. Here, we evaluate several candidate FCS methods that retain directional information. According to simulation results, the best-performing method involves the mean aggregation of probe limma t-statistics by gene followed by a rank-ANOVA enrichment test using the mitch package. This method, which we call 'LAM,' outperformed an existing over-representation analysis method in simulations, and showed higher sensitivity and robustness in an analysis of real lung tumour-normal paired datasets. Using matched RNA-seq data, we examine the relationship of methylation differences at promoters and gene bodies with RNA expression at the level of pathways in lung cancer. To demonstrate the utility of our approach, we apply it to three other contexts where public data were available. First, we examine the differential pathway methylation associated with chronological age. Second, we investigate pathway methylation differences in infants conceived with in vitro fertilization. Lastly, we analyse differential pathway methylation in 19 disease states, identifying hundreds of novel associations. These results show LAM is a powerful method for the detection of differential pathway methylation complementing existing methods. A reproducible vignette is provided to illustrate how to implement this method.

Indexed as

DNA MethylationLung NeoplasmsEpigenesis, GeneticFemaleGenome-Wide Association StudyHumansPromoter Regions, GeneticDNA methylationepigeneticsepigenome-wide association studyfunctional enrichment analysisInfinium ArrayPathway analysis

Identifiers

PMID38967555
PMCPMC11229754

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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.