Evidence map›Paper›PMID 31533352›Full record

ArticleGenes2019

Detection of Differentially Methylated Regions Using Bayes Factor for Ordinal Group Responses.

Fengjiao Dunbar, Hongyan Xu, Duchwan Ryu, Santu Ghosh, Huidong Shi, Varghese George

Abstract read
In one paragraph

Article in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

6 authors.

Fengjiao DunbarGenomics Research Center, AbbVie, North Chicago, IL 60064, USA. fengjiao.dunbar@abbvie.com.
Hongyan XuDepartment of Population Health Sciences, Augusta University, Augusta, GA 30912, USA. hxu@augusta.edu.
Duchwan RyuDepartment of Statistics and Actuarial Science, Northern Illinois University, DeKalb, IL 60178, USA. dryu@niu.edu.
Santu GhoshDepartment of Population Health Sciences, Augusta University, Augusta, GA 30912, USA. sghosh@augusta.edu.
Huidong ShiGeorgia Cancer Center, Augusta University, Augusta, GA 30912, USA. hshi@augusta.edu.
Varghese GeorgeDepartment of Population Health Sciences, Augusta University, Augusta, GA 30912, USA. vgeorge@augusta.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Researchers in genomics are increasingly interested in epigenetic factors such as DNA methylation, because they play an important role in regulating gene expression without changes in the DNA sequence. There have been significant advances in developing statistical methods to detect differentially methylated regions (DMRs) associated with binary disease status. Most of these methods are being developed for detecting differential methylation rates between cases and controls. We consider multiple severity levels of disease, and develop a Bayesian statistical method to detect the region with increasing (or decreasing) methylation rates as the disease severity increases. Patients are classified into more than two groups, based on the disease severity (e.g., stages of cancer), and DMRs are detected by using moving windows along the genome. Within each window, the Bayes factor is calculated to test the hypothesis of monotonic increase in methylation rates corresponding to severity of the disease versus no difference. A mixed-effect model is used to incorporate the correlation of methylation rates of nearby CpG sites in the region. Results from extensive simulation indicate that our proposed method is statistically valid and reasonably powerful. We demonstrate our approach on a bisulfite sequencing dataset from a chronic lymphocytic leukemia (CLL) study.

Indexed as

DNA MethylationBayes TheoremBiomarkers, TumorCpG IslandsGenomicsHumansNeoplasmsBiomarkers, TumorBayes factorBayesian mixed-effect modelCpG sitesDNA methylationOrdinal responses

Identifiers

PMID31533352
PMCPMC6770971

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.