Evidence map›Paper›PMID 39730483›Full record

ArticleScientific reports2024

Predicting human miRNA disease association with minimize matrix nuclear norm.

Ahmet Toprak

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

1 author.

Ahmet ToprakDepartment of Electricity and Energy, Selcuk University, Konya, Turkey. atoprak@selcuk.edu.tr.ORCID 0000-0003-3337-4917

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

microRNAs (miRNAs) are non-coding RNA molecules that influence the development and progression of many diseases. Research have documented that miRNAs have a significant role in the prevention, diagnosis, and treatment of complex human diseases. Recently, scientists have devoted extensive resources to attempting to find the connections between miRNAs and diseases. Since the experimental methods used to discover that new miRNA-disease associations are time-consuming and expensive, many computational methods have been developed. In this research, a novel computational method based on matrix decomposition was proposed to predict new associations between miRNAs and diseases. Furthermore, the nuclear norm minimization method was employed to acquire breast cancer-associated miRNAs. We then evaluated the effectiveness of our method by utilizing two different cross-validation techniques and the results were compared to seven different methods. Moreover, a case study on breast cancer further validated our technique, confirming its predictive accuracy. These experimental results demonstrate that our method is a reliable computational model for uncovering potential miRNA-disease relationships.

Indexed as

Breast NeoplasmsComputational BiologyMicroRNAsAlgorithmsFemaleGenetic Predisposition to DiseaseHumansMicroRNAsDiseaseMatrix decompositionMatrix nuclear normMiRNAMiRNA-disease associations

Identifiers

PMID39730483
PMCPMC11680809

What OpenQuestion holds

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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.