Evidence map›Paper›PMID 33568045›Full record

ArticleBMC bioinformatics2021

Detecting differentially methylated regions using a fast wavelet-based approach to functional association analysis.

William R P Denault, Astanand Jugessur

Erratum issuedAbstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 citing papers in PubMed.

  1. Article
  2. fSuSiE enables fine-mapping of QTLs from genome-scale molecular profiles.bioRxiv : the preprint server for biology · 2025
    Article
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

William R P DenaultDepartment of Genetics and Bioinformatics, Norwegian Institute of Public Health, Oslo, Norway. william.denault@fhi.no.ORCID http://orcid.org/0000-0002-9690-3890
Astanand JugessurDepartment of Genetics and Bioinformatics, Norwegian Institute of Public Health, Oslo, Norway.

Funding

Norges Forskningsråd 249779Norges Forskningsråd 262700
6 · The paper itself

Abstract

backgroundWe present here a computational shortcut to improve a powerful wavelet-based method by Shim and Stephens (Ann Appl Stat 9(2):665-686, 2015. https://doi.org/10.1214/14-AOAS776 ) called WaveQTL that was originally designed to identify DNase I hypersensitivity quantitative trait loci (dsQTL).

resultsWaveQTL relies on permutations to evaluate the significance of an association. We applied a recent method by Zhou and Guan (J Am Stat Assoc 113(523):1362-1371, 2017. https://doi.org/10.1080/01621459.2017.1328361 ) to boost computational speed, which involves calculating the distribution of Bayes factors and estimating the significance of an association by simulations rather than permutations. We called this simulation-based approach "fast functional wavelet" (FFW), and tested it on a publicly available DNA methylation (DNAm) dataset on colorectal cancer. The simulations confirmed a substantial gain in computational speed compared to the permutation-based approach in WaveQTL. Furthermore, we show that FFW controls the type I error satisfactorily and has good power for detecting differentially methylated regions.

conclusionsOur approach has broad utility and can be applied to detect associations between different types of functions and phenotypes. As more and more DNAm datasets are being made available through public repositories, an attractive application of FFW would be to re-analyze these data and identify associations that might have been missed by previous efforts. The full R package for FFW is freely available at GitHub https://github.com/william-denault/ffw .

Indexed as

DNA MethylationQuantitative Trait LociBayes TheoremComputer SimulationPhenotypeAssociation analysisDNA methylationEpigeneticsEWASWavelets

Identifiers

PMID33568045
PMCPMC7876806

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.