Evidence map›Paper›PMID 41470045›Full record

ReviewBriefings in bioinformatics2025

From nucleotides to numbers: a comprehensive review of RNA feature extraction methods for computational modelling.

Fatemeh Safari, Jai J Tree, Fatemeh Vafaee

Abstract readReview
In one paragraph

Review in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Fatemeh SafariSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Jai J TreeSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Fatemeh VafaeeSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.ORCID 0000-0002-7521-2417

Funding

Australian Research Council Discovery Project DP220101938the Australian Government Research Training Program (RTP) Scholarship
6 · The paper itself

Abstract

Machine learning is a powerful approach for analysing RNA sequences, particularly for understanding the function and regulation of noncoding RNAs. A critical step in this process is feature extraction, which transforms biological sequences into numerical representations that allow computational models to capture and interpret complex biological patterns. Despite its central role, the field of RNA feature extraction remains broad and fragmented, with limited standardization and accessibility hindering consistent application. In this comprehensive review, we address the fragmentation of the field by systematically organizing over 25 feature extraction strategies into sequence- and structure-based approaches. We further conduct a comparative analysis highlighting how the choice of feature sets impacts model performance, reinforcing the importance of integrated feature engineering. To facilitate practical adoption, it also provides a curated list of publicly available tools and software packages. By consolidating methodologies and resources, this work seeks to improve reproducibility, scalability, and interpretability in machine learning-driven RNA research.

Indexed as

Computational BiologyMachine LearningNucleotidesRNASequence Analysis, RNAComputer SimulationHumansSoftwareNucleotidesRNAfeature extractionmachine learningnon coding RNA (ncRNA)RNA bioinformaticssequence representation

Identifiers

PMID41470045
PMCPMC12753313

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.