Evidence map›Paper›PMID 40324334›Full record

ArticleBriefings in bioinformatics2025

GKNnet: an relational graph convolutional network-based method with knowledge-augmented activation layer for microbial structural variation detection.

Fengyi Guo, Yuanbo Li, Hongyuan Zhao, Xiaogang Liu, Jian Mao, Dongna Ma, Shuangping Liu

Abstract read
In one paragraph

Article in Briefings in 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

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. Article
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.

Fengyi GuoSchool of Artificial Intelligence and Computer Science, Jiangnan University, 1800 Lihu Avenue, Binhu District, Wuxi, Jiangsu 214122, China.
Yuanbo LiSchool of Artificial Intelligence and Computer Science, Jiangnan University, 1800 Lihu Avenue, Binhu District, Wuxi, Jiangsu 214122, China.
Hongyuan ZhaoNational Engineering Research Center of Cereal Fermentation and Food Biomanufacturing, State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Binhu District, Wuxi, Jiangsu 214122, China.
Xiaogang LiuLuzhou Laojiao Group Co. Ltd, 157 Guojiao Road, Jiangyang District, Luzhou 646000, Sichuan, China.
Jian MaoNational Engineering Research Center of Cereal Fermentation and Food Biomanufacturing, State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Binhu District, Wuxi, Jiangsu 214122, China.ORCID 0000-0002-3221-2492
Dongna MaNational Engineering Research Center of Cereal Fermentation and Food Biomanufacturing, State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Binhu District, Wuxi, Jiangsu 214122, China.
Shuangping LiuSchool of Artificial Intelligence and Computer Science, Jiangnan University, 1800 Lihu Avenue, Binhu District, Wuxi, Jiangsu 214122, China.

Funding

Fundamental Research Funds for the Central Universities JUSRP124005National Natural Science Foundation of China 22478159
6 · The paper itself

Abstract

Structural variants (SVs) in microbial genomes play a critical role in phenotypic changes, environmental adaptation, and species evolution, with deletion variations particularly closely linked to phenotypic traits. Therefore, accurate and comprehensive identification of deletion variations is essential. Although long-read sequencing technology can detect more SVs, its high error rate introduces substantial noise, leading to high false-positive and low recall rates in existing SV detection algorithms. This paper presents an SV detection method based on graph convolutional networks (GCNs). The model first represents node features through a heterogeneous graph, leveraging the GCN to precisely identify variant regions. Additionally, a knowledge-augmented activation layer (KANLayer) with a learnable activation function is introduced to reduce noise around variant regions, thereby improving model precision and reducing false positives. A clustering algorithm then aggregates multiple overlapping regions near the variant center into a single accurate SV interval, further enhancing recall. Validation on both simulated and real datasets demonstrates that our method achieves superior F1 scores compared to benchmark methods (cuteSV, Sniffles, Svim, and Pbsv), highlighting its advantage and robustness in SV detection and offering an innovative solution for microbial genome structural variation research.

Indexed as

Computational BiologyGenome, MicrobialGenomic Structural VariationNeural Networks, ComputerAlgorithmsgraph neural networkheterogeneous graphlong-read sequencingstructural variation detection

Identifiers

PMID40324334
PMCPMC12052243

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.