Evidence map›Paper›PMID 40846991›Full record

ArticleHuman genomics2025

Flu-CNN: identifying host specificity of Influenza A virus using convolutional networks.

Mingda Hu, Nan Luo, Boqian Wang, Renjie Meng, Yunxiang Zhao, Zili Chai, Yuan Jin, Junjie Yue, Xin Wang, Wei Chen and 1 more

Abstract read
In one paragraph

Article in Human genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

11 authors.

Mingda Hu *Beijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China.
Nan Luo *Beijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China.
Boqian WangBeijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China.
Renjie MengBeijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China.
Yunxiang ZhaoBeijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China.
Zili ChaiBeijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China.
Yuan JinBeijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China.
Junjie YueBeijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China.
Xin WangBeijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China. dywangxin@foxmail.com.
Wei ChenCollege of Computer, National University of Defense Technology, Changsha, China. chenwei@nudt.edu.cn.
Hongguang RenBeijing Institute of Biotechnology, State Key Laboratory of Advanced Biotechnology, Beijing, China. bioren@163.com.

Funding

National Natural Science Foundation of China 31800136National Natural Science Foundation of China 32070025National Natural Science Foundation of China 62206309
6 · The paper itself

Abstract

Influenza A viruses (IAVs) have historically posed significant public health threats, causing severe pandemics. Viral host specificity is typically constrained by host barriers, limiting the range of species that can be infected. However, these barriers are not absolute, and occasionally, cross-species transmission occurs, leading to human outbreaks. Early identification of changes in IAV host specificity is, therefore, critical. Despite advancements, identifying host susceptibility from genomic sequences during outbreaks remains challenging. Timely predictions are critical for effective real-time outbreak management and risk mitigation during the early stages of an epidemic. To address this, we proposed Flu-level Convolutional Neural Networks (Flu-CNN), a model designed to analyze genomic segments and identify IAV host specificity, with a particular focus on avian influenza viruses that could potentially infect humans. Extensive evaluations on large-scale genomic datasets containing 911,098 sequences show that Flu-CNN achieves an impressive 99% accuracy in determining host specificity from a single genomic segment, even for high-risk subtypes like H5N1, H7N9, and H9N2, which have a limited number of viral strains. Given its high level of accuracy, the model was applied to identify key mutations and assess the zoonotic potential of these strains. Furthermore, our study presents a pioneering approach for predicting IAV host specificity, offering novel insights into the evolutionary trajectory of these viruses. The model's significance extends beyond evolutionary analysis, playing a pivotal role in outbreak surveillance and contributing to efforts aimed at preventing the viral spread on a global scale.

Indexed as

Host SpecificityInfluenza A virusInfluenza, HumanNeural Networks, ComputerAnimalsBirdsGenome, ViralHumansInfluenza in BirdsDeep learningHost specificityInfluenza A virusLarge-scale genomic dataZoonotic strains

Identifiers

PMID40846991
PMCPMC12374346

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LicenceCC BY-NC-ND
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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.