Evidence map›Paper›PMID 41554052›Full record

ReviewBriefings in bioinformatics2026

From biogenesis to deep modeling: a holistic review of miRNA-disease prediction computational methods with experimental comparison.

Siya Xie, K L Eddie Law

Abstract readReview
In one paragraph

Review in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Siya XieFaculty of Applied Sciences, Macao Polytechnic University, Macao 999078, SAR, China.ORCID 0009-0004-8323-9160
K L Eddie LawFaculty of Applied Sciences, Macao Polytechnic University, Macao 999078, SAR, China.ORCID 0000-0003-0377-3810

Funding

Heilongjiang Provincial Higher Education Basic Scientific Research Foundation 1453QN019Macao Polytechnic University RP/FCA-05/2025New Era Longjiang Outstanding Master's and Doctoral Dissertation Foundation LJYXL2023-086
6 · The paper itself

Abstract

Abnormal dysregulation of microRNAs (miRNAs) expression may lead to a wide spectrum of diseases, and as miRNAs play pivotal roles in disease pathogenesis, diagnosis, and therapy, identifying potential miRNA-disease associations (MDAs) is essential for discovering new diagnostic biomarkers, developing targeted therapeutic strategies, and advancing personalized medicine. Traditional wet-lab experiments are time-consuming, expensive, and consume a lot of resources. Hence, various computational approaches should be developed as auxiliary a priori tools. In the following text, we compile different methods proposed for MDA prediction over the past decade. First, we analyze the data resources supporting MDA studies and introduce approaches for quantifying similarities among MDAs. Second, we comprehensively review 66 computational methods, classify them into five categories, and present comparative experimental analyses on selected methods to identify future research directions. To enhance accessibility, we upload a summary of discussed methods to a GitHub repository (https://github.com/xiesiya/miRNA-disease-association-methods). This review provides comprehensive background knowledge on computational methods for future MDA prediction research.

Indexed as

Computational BiologyDeep LearningGenetic Predisposition to DiseaseMicroRNAsHumansMicroRNAscomputational methodsMDA predictionmicroRNAmiRNA–disease association

Identifiers

PMID41554052
PMCPMC12814990

What OpenQuestion holds

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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.