Evidence map›Paper›PMID 41646832›Full record

ArticleFrontiers in genetics2026

DFL-MHC: MHC identification model based on dual-stage training and multi-view feature fusion.

Yanjuan Li, Yiben Lin, Dong Chen

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Article in Frontiers in genetics, 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

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3 authors.

Yanjuan LiCollege of Electrical and Information Engineering, Quzhou University, Quzhou, China.
Yiben LinSchool of Computer Science, Hangzhou Dianzi University, Hangzhou, China.
Dong ChenCollege of Electrical and Information Engineering, Quzhou University, Quzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The major histocompatibility complex (MHC) is the central genetic basis of adaptive immune responses, it plays a crucial role in antigen presentation, immune surveillance, and susceptibility to various diseases. Therefore, accurate MHC identification is essential for both immunological research and clinical applications. Most existing methods still depend on manually engineered features or a single protein language model (PLM for short), these methods cannot perfectly capture complementary information across sequence lengths or across different PLMs. Furthermore, most existing methods often adopt conventional machine learning algorithms or simple multilayer perceptron (MLP) classifiers to construct identification model, they have no ability to model deep semantic dependencies within sequences. To overcome these limitations, we introduce an MHC identification model based on dual-stage training and multi-view feature fusion, termed DFL-MHC, a novel framework that unifies multi-sequence and multi-model views within a dual-stage training strategy. In the feature extraction stage, we design a cross-sequence and cross-model multi-view scheme. In this scheme, a protein sequence is truncated into two different residue sequences with a length of 1,022, two PLMs are respectively employed to extract features from the two different residue sequences, these extracted features are fused to represent the protein sequence. The dimensionality reduction algorithm is applied to the fused features and obtain the optimal feature subset. The optimal feature subset can fully capture complementary information across sequence lengths and across different PLMs. In the feature modeling stage, we construct a bi-directional long short-term memory (BiLSTM) network incorporating an attention mechanism to capture long-range dependencies and deep semantic dependencies within sequences. On the MHC identification task, DFL-MHC achieves better performance than the existing methods. It is demonstrated that the effectiveness of leveraging both multi-view feature fusion and dual-stage training to achieve accurate and reliable MHC identification.

Indexed as

dimensionality reductiondual stage trainingfeature extractionmajor histocompatibility complex (MHC)protein identification

Identifiers

PMID41646832
PMCPMC12868131

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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.