Evidence map›Paper›PMID 28476023›Full record

ArticleOncotarget2017

iRNAm5C-PseDNC: identifying RNA 5-methylcytosine sites by incorporating physical-chemical properties into pseudo dinucleotide composition.

Wang-Ren Qiu, Shi-Yu Jiang, Zhao-Chun Xu, Xuan Xiao, Kuo-Chen Chou

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
17.4field-weighted citation impact, top 1% 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

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

62 citing papers in PubMed, 214 citations in OpenAlex.

  1. Article
  2. Detection, molecular function and mechanisms of m5C in cancer.Clinical and translational medicine · 2025
    Review
  3. Article
  4. m5CStack: An integrated framework for m5C site prediction using multi-feature stacking.Computational and structural biotechnology journal · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. XGBoost framework with feature selection for the prediction of RNA N5-methylcytosine sites.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  12. m6A-TSHub: Unveiling the Context-specific mGenomics, proteomics & bioinformatics · 2023
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. NSUN2-mediated RNA mEpigenetics · 2022
    Article
  18. Article
  19. Review
  20. Article

2 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 3 countries.

Wang-Ren QiuDepartment of Computer Science and Bond Life Science Center, University of Missouri, Columbia, MO, USA.
Shi-Yu JiangComputer Department, Jingdezhen Ceramic Institute, Jingdezhen, China.
Zhao-Chun XuComputer Department, Jingdezhen Ceramic Institute, Jingdezhen, China.
Xuan XiaoComputer Department, Jingdezhen Ceramic Institute, Jingdezhen, China.
Kuo-Chen ChouGordon Life Science Institute, Boston, Massachusetts, USA.
Jingdezhen Ceramic Institute · CNKing Abdulaziz University · SAUniversity of Missouri · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Occurring at cytosine (C) of RNA, 5-methylcytosine (m5C) is an important post-transcriptional modification (PTCM). The modification plays significant roles in biological processes by regulating RNA metabolism in both eukaryotes and prokaryotes. It may also, however, cause cancers and other major diseases. Given an uncharacterized RNA sequence that contains many C residues, can we identify which one of them can be of m5C modification, and which one cannot? It is no doubt a crucial problem, particularly with the explosive growth of RNA sequences in the postgenomic age. Unfortunately, so far no user-friendly web-server whatsoever has been developed to address such a problem. To meet the increasingly high demand from most experimental scientists working in the area of drug development, we have developed a new predictor called iRNAm5C-PseDNC by incorporating ten types of physical-chemical properties into pseudo dinucleotide composition via the auto/cross-covariance approach. Rigorous jackknife tests show that its anticipated accuracy is quite high. For most experimental scientists' convenience, a user-friendly web-server for the predictor has been provided at http://www.jci-bioinfo.cn/iRNAm5C-PseDNC along with a step-by-step user guide, by which users can easily obtain their desired results without the need to go through the complicated mathematical equations involved. It has not escaped our notice that the approach presented here can also be used to deal with many other problems in genome analysis.

Indexed as

Algorithms5-MethylcytosineBase SequenceChemical PhenomenaComputational BiologyInternetModels, MolecularNucleic Acid ConformationNucleotidesReproducibility of ResultsRNA5-MethylcytosineNucleotidesRNAauto/cross-covariancephysical-chemical property matrixpseudo dinucleotide compositionRNA 5-methylcytosine sitesweb-server

Identifiers

PMID28476023
PMCPMC5522291
OpenAlexW2607378088

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.