Evidence map›Paper›PMID 33294291›Full record

ArticleMolecular therapy. Nucleic acids2020

Predicting Preference of Transcription Factors for Methylated DNA Using Sequence Information.

Meng-Lu Liu, Wei Su, Jia-Shu Wang, Yu-He Yang, Hui Yang, Hao Lin

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
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  9. Identification ofComputational and mathematical methods in medicine · 2022
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  13. Review
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.

Meng-Lu LiuCenter for Informational Biology, University of Electronic Science and Technology of China, Chengdu 610054, China.
Wei SuCenter for Informational Biology, University of Electronic Science and Technology of China, Chengdu 610054, China.
Jia-Shu WangCenter for Informational Biology, University of Electronic Science and Technology of China, Chengdu 610054, China.
Yu-He YangCenter for Informational Biology, University of Electronic Science and Technology of China, Chengdu 610054, China.
Hui YangCenter for Informational Biology, University of Electronic Science and Technology of China, Chengdu 610054, China.
Hao LinCenter for Informational Biology, University of Electronic Science and Technology of China, Chengdu 610054, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factors play key roles in cell-fate decisions by regulating 3D genome conformation and gene expression. The traditional view is that methylation of DNA hinders transcription factors binding to them, but recent research has shown that many transcription factors prefer to bind to methylated DNA. Therefore, identifying such transcription factors and understanding their functions is a stepping-stone for studying methylation-mediated biological processes. In this paper, a two-step discriminated method was proposed to recognize transcription factors and their preference for methylated DNA based only on sequences information. In the first step, the proposed model was used to discriminate transcription factors from non-transcription factors. The areas under the curve (AUCs) are 0.9183 and 0.9116, respectively, for the 5-fold cross-validation test and independent dataset test. Subsequently, for the classification of transcription factors that prefer methylated DNA and transcription factors that prefer non-methylated DNA, our model could produce the AUCs of 0.7744 and 0.7356, respectively, for the 5-fold cross-validation test and independent dataset test. Based on the proposed model, a user-friendly web server called TFPred was built, which can be freely accessed at http://lin-group.cn/server/TFPred/.

Indexed as

machine learningmethylated DNAsequence featuretranscription factorsweb server

Identifiers

PMID33294291
PMCPMC7691157

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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.