Evidence map›Paper›PMID 32414326›Full record

ArticleBMC genomics2020

PretiMeth: precise prediction models for DNA methylation based on single methylation mark.

Jianxiong Tang, Jianxiao Zou, Xiaoran Zhang, Mei Fan, Qi Tian, Shuyao Fu, Shihong Gao, Shicai Fan

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 38% of its field
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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Jianxiong TangSchool of Automation Engineering, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Jianxiao ZouSchool of Automation Engineering, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Xiaoran ZhangSchool of Automation Engineering, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Mei FanChengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Qi TianSchool of Automation Engineering, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Shuyao FuSchool of Automation Engineering, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Shihong GaoSchool of Automation Engineering, University of Electronic Science and Technology of China, Chengdu, 611731, China.
Shicai FanSchool of Automation Engineering, University of Electronic Science and Technology of China, Chengdu, 611731, China. shicaifan@uestc.edu.cn.
University of Electronic Science and Technology of China · CN

Funding

Sichuan Province Youth Science and Technology Innovation Team 2015TD0018Sichuan Science and Technology Program 2018HH0149the National Natural Science Foundation of China 61872063
6 · The paper itself

Abstract

backgroundThe computational prediction of methylation levels at single CpG resolution is promising to explore the methylation levels of CpGs uncovered by existing array techniques, especially for the 450 K beadchip array data with huge reserves. General prediction models concentrate on improving the overall prediction accuracy for the bulk of CpG loci while neglecting whether each locus is precisely predicted. This leads to the limited application of the prediction results, especially when performing downstream analysis with high precision requirements.

resultsHere we reported PretiMeth, a method for constructing precise prediction models for each single CpG locus. PretiMeth used a logistic regression algorithm to build a prediction model for each interested locus. Only one DNA methylation feature that shared the most similar methylation pattern with the CpG locus to be predicted was applied in the model. We found that PretiMeth outperformed other algorithms in the prediction accuracy, and kept robust across platforms and cell types. Furthermore, PretiMeth was applied to The Cancer Genome Atlas data (TCGA), the intensive analysis based on precise prediction results showed that several CpG loci and genes (differentially methylated between the tumor and normal samples) were worthy for further biological validation.

conclusionThe precise prediction of single CpG locus is important for both methylation array data expansion and downstream analysis of prediction results. PretiMeth achieved precise modeling for each CpG locus by using only one significant feature, which also suggested that our precise prediction models could be probably used for reference in the probe set design when the DNA methylation beadchip update. PretiMeth is provided as an open source tool via https://github.com/JxTang-bioinformatics/PretiMeth.

Indexed as

DNA MethylationModels, GeneticCpG IslandsEpigenomicsGenetic LociGenomeHumansLogistic ModelsNeoplasmsSequence Analysis, DNADifferential methylationDNA methylationLogistic regressionPrecise predictionSingle-locus modelingTCGA

Identifiers

PMID32414326
PMCPMC7227319
OpenAlexW3027055147

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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.