Evidence map›Paper›PMID 33203349›Full record

ArticleBMC bioinformatics2020

MADA: a web service for analysing DNA methylation array data.

Xinyu Hu, Li Tang, Linconghua Wang, Fang-Xiang Wu, Min Li

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Methods in DNA methylation array dataset analysis: A review.Computational and structural biotechnology journal · 2024
    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

5 authors.

Xinyu HuSchool of Computer Science and Engineering, Central South University, Changsha, China.
Li TangSchool of Computer Science and Engineering, Central South University, Changsha, China.
Linconghua WangSchool of Computer Science and Engineering, Central South University, Changsha, China.
Fang-Xiang WuDivision of Biomedical Engineering and Department of Mechanical Engineering, University of Saskatchewan, Saskatoon, SKS7N5A9, Canada.
Min LiSchool of Computer Science and Engineering, Central South University, Changsha, China. limin@csu.edu.cn.ORCID http://orcid.org/0000-0002-0188-1394

Funding

National Natural Science Foundation of China 61732009
6 · The paper itself

Abstract

backgroundDNA methylation in the human genome is acknowledged to be widely associated with biological processes and complex diseases. The Illumina Infinium methylation arrays have been approved as one of the most efficient and universal technologies to investigate the whole genome changes of methylation patterns. As methylation arrays may still be the dominant method for detecting methylation in the anticipated future, it is crucial to develop a reliable workflow to analysis methylation array data.

resultsIn this study, we develop a web service MADA for the whole process of methylation arrays data analysis, which includes the steps of a comprehensive differential methylation analysis pipeline: pre-processing (data loading, quality control, data filtering, and normalization), batch effect correction, differential methylation analysis, and downstream analysis. In addition, we provide the visualization of pre-processing, differentially methylated probes or regions, gene ontology, pathway and cluster analysis results. Moreover, a customization function for users to define their own workflow is also provided in MADA.

conclusionsWith the analysis of two case studies, we have shown that MADA can complete the whole procedure of methylation array data analysis. MADA provides a graphical user interface and enables users with no computational skills and limited bioinformatics background to carry on complicated methylation array data analysis. The web server is available at: http://120.24.94.89:8080/MADA.

Indexed as

DNA MethylationGenome, HumanOligonucleotide Array Sequence AnalysisComputational BiologyCpG IslandsHumansInternetDifferential methylation analysisDNA methylationDownstream analysisNormalization

Identifiers

PMID33203349
PMCPMC7672854

What OpenQuestion holds

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LicenceCC BY
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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.