Evidence map›Paper›PMID 40263997›Full record

ArticleBMC bioinformatics2025

HPOseq: a deep ensemble model for predicting the protein-phenotype relationships based on protein sequences.

Kai Zhao, Zhuocheng Ji, Linlin Zhang, Na Quan, Yuheng Li, Guanglei Yu, Xuehua Bi

Abstract read
In one paragraph

Article in BMC bioinformatics, 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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Kai ZhaoSchool of Computer Science and Technology, Xinjiang University, Urumqi, 830011, China.
Zhuocheng JiSchool of Computer Science and Technology, Xinjiang University, Urumqi, 830011, China.
Linlin ZhangSchool of Software, Xinjiang University, Urumqi, 830011, China.
Na QuanSchool of Computer Science and Technology, Xinjiang University, Urumqi, 830011, China.
Yuheng LiSchool of Computer Science and Technology, Xinjiang University, Urumqi, 830011, China.
Guanglei YuCollege of Medical Engineering and Technology, Xinjiang Medical University, Urumqi, 830011, China.
Xuehua BiCollege of Medical Engineering and Technology, Xinjiang Medical University, Urumqi, 830011, China. bxh0327@foxmail.com.

Funding

the Key R&D Program of Xinjiang Uygur Autonomous Regin 2022B03023the Natural Science Foundation of China 62366052the Natural Science Foundation of Xinjiang Uygur Autonomous Regin 2024D01C126
6 · The paper itself

Abstract

backgroundUnderstanding the relationships between proteins and specific disease phenotypes contributes to the early detection of diseases and advances the development of personalized medicine. The acquisition of a large amount of proteomics data has facilitated this process. To improve discovery efficiency and reduce the time and financial costs associated with biological experiments, various computational methods have yielded promising results. However, the lack of rich and reliable protein-related information still presents challenges in this process.

resultsIn this paper, we propose an ensemble prediction model, named HPOseq, which predicts human protein-phenotype relationships based only on sequence information. HPOseq establishes two base models to achieve objectives. One directly extracts internal information from amino acid sequences as protein features to predict the associated phenotypes. The other builds a protein-protein network based on sequence similarity, extracting information between proteins for phenotype prediction. Ultimately, an ensemble module is employed to integrate the predictions from both base models, resulting in the final prediction.

conclusionThe results of 5-fold cross-validation reveal that HPOseq outperforms seven baseline methods for predicting protein-phenotype relationships. Moreover, we conduct case studies from the points of phenotype annotation and protein analysis to verify the practical significance of HPOseq.

Indexed as

Computational BiologyProteinsSequence Analysis, ProteinAlgorithmsAmino Acid SequenceDatabases, ProteinHumansPhenotypeProteinsAmino acid sequenceDeep learningEnsemble modelVariational graph autoencoder

Identifiers

PMID40263997
PMCPMC12013097

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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.