Evidence map›Paper›PMID 40060867›Full record

ArticleACS omega2025

XGBMUT: Predicting the Functional Impact of Missense Mutations Using an Extreme Gradient Boost Classifier.

Gabriel Rodrigues Coutinho Pereira, Loiane Mendonça Abrantes Da Conceição, Bárbara de Azevedo Abrahim-Vieira, Carlos Rangel Rodrigues, Lucio Mendes Cabral, Ricardo Limongi França Coelho, Joelma Freire De Mesquita

Abstract read
In one paragraph

Article in ACS omega, 2025. 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. Review
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

7 authors.

Gabriel Rodrigues Coutinho PereiraLaboratory of Molecular Modeling and QSAR, Faculty of Pharmacy, Federal University of Rio de Janeiro, 373 Carlos Chagas Filho Avenue, Rio de Janeiro, Rio de Janeiro 21941-170, Brazil.
Loiane Mendonça Abrantes Da ConceiçãoLaboratory of Bioinformatics and Computational Biology, Biomedical Institute, Federal University of the State of Rio de Janeiro, 296 Pasteur Avenue, Rio de Janeiro, Rio de Janeiro 22290-240, Brazil.ORCID https://orcid.org/0000-0002-5386-6997
Bárbara de Azevedo Abrahim-VieiraLaboratory of Molecular Modeling and QSAR, Faculty of Pharmacy, Federal University of Rio de Janeiro, 373 Carlos Chagas Filho Avenue, Rio de Janeiro, Rio de Janeiro 21941-170, Brazil.
Carlos Rangel RodriguesLaboratory of Molecular Modeling and QSAR, Faculty of Pharmacy, Federal University of Rio de Janeiro, 373 Carlos Chagas Filho Avenue, Rio de Janeiro, Rio de Janeiro 21941-170, Brazil.
Lucio Mendes CabralLaboratory of Industrial Pharmaceutical Technology, Faculty of Pharmacy, Federal University of Rio de Janeiro, 373 Carlos Chagas Filho Avenue, Rio de Janeiro, Rio de Janeiro 21941-170, Brazil.
Ricardo Limongi França CoelhoFaculty of Business Administration, Accountability and Economics, Federal University of Goiás, Samambaia Street, Goiânia, Goiás 74001-970, Brazil.
Joelma Freire De MesquitaLaboratory of Bioinformatics and Computational Biology, Biomedical Institute, Federal University of the State of Rio de Janeiro, 296 Pasteur Avenue, Rio de Janeiro, Rio de Janeiro 22290-240, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Millions of new mutations have been discovered largely due to advancements in genome projects, but characterizing their effects through traditional wet-lab experiments remains labor-intensive and time-consuming. Functional prediction algorithms offer a solution by enabling the efficient screening of mutations, thereby saving time and resources. The objective of this study was to develop a competitive algorithm for predicting the functional impact of missense mutations. A unified database and substitution matrices containing predictor variables specifically for missense mutations were initially constructed. Subsequently, values for the predictor variables were collected from the training and test sets derived from the ClinVar and HumsaVar databases. A series of supervised machine learning classifiers were then trained, and their performance was evaluated using the test set. The best-performing model was additionally compared against ten currently available functional prediction algorithms. The proposed algorithm, XGBMut, demonstrates exceptional accuracy in classifying missense mutations while also exhibiting a competitive performance. Additionally, a user-friendly graphical interface was developed to enhance accessibility for professionals in various fields. Unlike most existing methods, XGBMut eliminates the need for a web server dependency and the installation of third-party software, making it a more versatile tool for users.

Identifiers

PMID40060867
PMCPMC11886911

What Socratic 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 Socratic graph.