Evidence map›Paper›PMID 42331882›Full record

ArticleScientific reports2026

A multi-label cascade flexible neural forest model for predicting the subcellular location of multi-site bacterial proteins.

Lianxin Zhong, Yang Li, Yanhui Cheng, Guangchang Han, Anqi Li

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Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Lianxin ZhongTaishan College of Science and Technology, Tai'an, 271038, China.
Yang LiTaishan College of Science and Technology, Tai'an, 271038, China.
Yanhui ChengTaishan College of Science and Technology, Tai'an, 271038, China. YanhuiChengtk@163.com.
Guangchang HanTaishan College of Science and Technology, Tai'an, 271038, China.
Anqi LiTaishan College of Science and Technology, Tai'an, 271038, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Predicting the subcellular localization of multi-site bacterial proteins remains challenging because label correlations, limited sample size, and low sequence similarity reduce the effectiveness of conventional multi-label classifiers. In this study, we propose a multi-label cascade flexible neural forest (MLCFN Forest) that combines label-powerset-style coding-classification-decoding with a cascade ensemble of flexible neural tree (FNT) groups. The framework preserves label dependencies, decomposes the induced multi-class task into coordinated binary FNT outputs, and progressively reallocates model capacity to low-confidence samples through confidence-guided sample propagation and feature enhancement across layers. We explicitly note that the cascade FNT backbone builds on our previous CFNForest studies for cancer subtype classification, whereas the present work adapts that backbone to multi-label bacterial protein localization by introducing label-set encoding/decoding, multiclass FNT grouping, and a multi-site protein subcellular localization evaluation workflow. Using Gram-negative and Gram-positive benchmark datasets together with AECA-PSSM and PSSM-DWT features, MLCFN Forest consistently outperformed ML-RBF, ML-KNN, ML-LOC, INSDIF, and MLASSO under jackknife evaluation. For example, it achieved OLA/OAA values of 78.3%/76.4% on the Gram-negative AECA-PSSM dataset, 80.7%/78.5% on the Gram-negative PSSM-DWT dataset, and 80.2%/77.6% on the Gram-positive AECA-PSSM dataset. PCA-based low-dimensional experiments further suggested that the model retained good predictive ability after substantial dimensionality reduction. The present study is limited to classical benchmark datasets and does not yet include an independent external test set, strict nested model selection, or direct benchmarking against protein language model predictors; these points are therefore discussed as limitations and future directions.

Indexed as

Bacterial ProteinsComputational BiologyNeural Networks, ComputerRandom ForestSubcellular FractionsBacterial ProteinsCascade forestEnsemble modelFlexible neural treeLabel correlationMulti-label protein subcellular localization

Identifiers

PMID42331882
PMCPMC13575143

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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.