Evidence map›Paper›PMID 39242695›Full record

ArticleScientific reports2024

A hybrid residue based sequential encoding mechanism with XGBoost improved ensemble model for identifying 5-hydroxymethylcytosine modifications.

Islam Uddin, Hamid Hussain Awan, Majdi Khalid, Salman Khan, Shahid Akbar, Mahidur R Sarker, Maher G M Abdolrasol, Thamer A H Alghamdi

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. OptimDase: An Algorithm for Predicting DNA Binding Sites with Combined Feature Encoding.Interdisciplinary sciences, computational life sciences · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

8 authors.

Islam UddinDepartment of Computer Science, Abdul Wali Khan University, Mardan, Pakistan.
Hamid Hussain AwanDepartment of Computer Science, Muslim Youth University, Islamabad, Pakistan.
Majdi KhalidDepartment of Computer Science and Artificial Intelligence, College of Computing, Umm Al-Qura University, Makkah, 21955, Saudi Arabia.
Salman KhanDepartment of Computer Science, Abdul Wali Khan University, Mardan, Pakistan.
Shahid AkbarDepartment of Computer Science, Abdul Wali Khan University, Mardan, Pakistan. shahid.akbar@awkum.edu.pk.
Mahidur R SarkerInstitute of Visual Informatics, Universiti Kebangsaan Malaysia, Bangi, 43600, Selangor, Malaysia.
Maher G M AbdolrasolInstitute of Sustainable Energy, Universiti Tenaga Nasional, Kajang, 43000, Malaysia.
Thamer A H AlghamdiWolfson Centre for Magnetics, School of Engineering, Cardiff University, Cardiff, CF24 3AA, UK. alghamdit1@cardiff.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA modifications play an important role in actively controlling recently created formation in cellular regulation mechanisms, which link them to gene expression and protein. The RNA modifications have numerous alterations, presenting broad glimpses of RNA's operations and character. The modification process by the TET enzyme oxidation is the crucial change associated with cytosine hydroxymethylation. The effect of CR is an alteration in specific biochemical ways of the organism, such as gene expression and epigenetic alterations. Traditional laboratory systems that identify 5-hydroxymethylcytosine (5hmC) samples are expensive and time-consuming compared to other methods. To address this challenge, the paper proposed XGB5hmC, a machine learning algorithm based on a robust gradient boosting algorithm (XGBoost), with different residue based formulation methods to identify 5hmC samples. Their results were amalgamated, and six different frequency residue based encoding features were fused to form a hybrid vector in order to enhance model discrimination capabilities. In addition, the proposed model incorporates SHAP (Shapley Additive Explanations) based feature selection to demonstrate model interpretability by highlighting the high contributory features. Among the applied machine learning algorithms, the XGBoost ensemble model using the tenfold cross-validation test achieved improved results than existing state-of-the-art models. Our model reported an accuracy of 89.97%, sensitivity of 87.78%, specificity of 94.45%, F1-score of 0.8934%, and MCC of 0.8764%. This study highlights the potential to provide valuable insights for enhancing medical assessment and treatment protocols, representing a significant advancement in RNA modification analysis.

Indexed as

5-MethylcytosineAlgorithmsMachine LearningCytosineHumans5-hydroxymethylcytosine5-MethylcytosineCytosine5-HydroxymethylcytosineCancerCardiovascular diseasesMachine learningRNA modificationsTET enzymeXGBoost

Identifiers

PMID39242695
PMCPMC11379919

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.