Fuguo Liu

Prof. Fuguo Liu


Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 September 2024 in Polymers
Verified
Journal Article
Open access
PDF file
FLFuguo Liu
Fuguo Liu
ZCZiru Chen
Ziru Chen
Jun XuJun Xu
Jun Xu
YZYanyan Zheng
Yanyan Zheng
WSWenyi Su
Wenyi Su
GLGuodong Li
Guodong Li
Three-dimensional printing technology is a rapid prototyping technology that has been widely used in manufacturing. However, the printing parameters in the 3D printing process have an important impact on the printing effect, so these parameters need to be optimized to obtain the best printing effect. In order to further understand the impact of 3D printing parameters on the printing effect, make theoretical explanations from the dimensions of mathematical models, and clarify the rationality of certain important parameters in previous experience, the purpose of this study is to predict the impact of 3D printing parameters on the printing effect by using machine learning methods. Specifically, we used four machine learning algorithms: SVR (support vector regression): A regression method that uses the principle of structural risk minimization to find a hyperplane in a high-dimensional space that best fits the data, with the goal of minimizing the generalization error bound. Random forest: An ensemble learning method that constructs a multitude of decision trees and outputs the class that is the mode of the classes (classification) or mean prediction (regression) of the individual trees. GBDT (gradient boosting decision tree): An iterative ensemble technique that combines multiple weak prediction models (decision trees) into a strong one by sequentially minimizing the loss function. Each subsequent tree is built to correct the errors of the previous tree. XGB (extreme gradient boosting): An optimized and efficient implementation of gradient boosting that incorporates various techniques to improve the performance of gradient boosting frameworks, such as regularization and sparsity-aware splitting algorithms. The influence of the print parameters on the results under the feature importance and SHAP (Shapley additive explanation) values is compared to determine which parameters have the greatest impact on the print effect. We also used feature importance and SHAP values to compare the importance impact of print parameters on results. In the experiment, we used a dataset with multiple parameters and divided it into a training set and a test set. Through Bayesian optimization and grid search, we determined the best hyperparameters for each algorithm and used the best model to make predictions for the test set. We compare the predictive performance of each model and confirm that the extrusion expansion ratio, elastic modulus, and elongation at break have the greatest influence on the printing effect, which is consistent with the experience. In future, we will continue to delve into methods for optimizing 3D printing parameters and explore how interpretive machine learning can be applied to the 3D printing process to achieve more efficient and reliable printing results.

3 June 2026 in PLOS ONE
Verified
Journal Article
Open access
PDF file
FLFuguo Liu
Fuguo Liu
TLTingLian Lai
TingLian Lai
WXWenXia Xu
WenXia Xu
GLGuodong Li
Guodong Li
Accurate functional annotation of viral proteins is essential for genomic surveillance, yet rapid viral evolution causes “functional drift” that challenges conventional sequence-only models. These models often lack interpretability and struggle with fragmented sequences from complex environmental samples such as wastewater. We developed ViralMultiNet, a structure-aware multimodal framework that integrates multi-scale k-mer encodings (4–7-mers) with functional semantic embeddings derived from UniProt annotations. Using a curated Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) dataset of 66,011 samples from wastewater metagenomics (NCBI SRA: SRX28474964), we implemented gated multimodal fusion and triple knowledge distillation to transfer structural insights from a teacher to a student model. Model performance was evaluated via 5-fold cross-validation and external validation on emerging variants. Training efficiency was optimized using Low-Rank Adaptation and Flash Attention. ViralMultiNet achieved robust classification performance with a macro F1 score of 0.921 ± 0.004, accuracy of 0.928 ± 0.003, and AUC of 0.983 in cross-validation. The distilled student model matched teacher performance within a negligible margin (<0.003 F1 difference) while reducing training time by 40.4% (from 94.3 to 56.2 minutes per epoch). Interpretability analysis revealed that model attention peaks consistently aligned with experimentally validated functional domains of the SARS-CoV-2 Spike protein, including the receptor-binding domain (residues 319–541), S1/S2 cleavage site (681–685), and fusion peptide (816–835). ViralMultiNet offers a scalable, interpretable solution for viral protein function prediction. Its ability to generalize across variants and map attention to critical biological regions supports deployment in wastewater-based early warning systems, enhancing global pandemic preparedness.

26 December 2024 in International Journal of Financial Engineering
Verified
Journal Article
Closed access
YLYuanmeng Liu
Yuanmeng Liu
FLFuguo Liu
Fuguo Liu
YSYufeng Shi
Yufeng Shi
YZYuxue Zhang
Yuxue Zhang
YLYijia Liu
Yijia Liu

9 June 2026 in Viruses
Verified
Journal Article
Open access
PDF file
TLTinglian Lai
Tinglian Lai
FLFuguo Liu
Fuguo Liu
GLGuodong Li
Guodong Li
LHLiyan Hua
Liyan Hua
Accurate viral protein function annotation is essential for genomic surveillance, yet conventional retrieval-augmented generation (RAG) pipelines often fragment biological evidence into fixed-length text chunks, disrupting relationships among ORFs, annotations, structural domains, sequence motifs, residue mappings, and model-derived attention evidence. We propose ViroBioTree, a tree-structured biological evidence retrieval framework for downstream viral protein evidence review rather than a new primary annotation classifier. Built as an evidence organization layer on ViralMultiNet-derived ORF-level predictions and annotations, ViroBioTree converts sequence, annotation, structure, and attention evidence into typed biological nodes and traceable edges, then performs deterministic multi-channel recall, evidence-aware reranking, balanced TopK selection, rule-based verification, and node-cited report generation. In a demo benchmark, ViroBioTree achieved its strongest deterministic proxy performance on structure-explanation tasks, with Precision@K = 1.0, Recall@K = 1.0, and diversity = 0.52; these values reflect expected node-type and tag agreement rather than independent biological correctness. A bounded full-scale SARS-CoV-2 index contained 39,800 ORF rows, 80,000 attention records, 199,418 nodes, and 495,886 edges. In a stratified full20k diagnostic evaluation, ViroBioTree showed task-dependent advantages over LlamaIndex vector retrieval for conflict detection, evidence retrieval, and structure explanation, while LlamaIndex remained competitive or stronger for annotation-rich function annotation. A cross-family Influenza A Virus (IAV) diagnostic audit showed that the schema can represent IAV evidence namespaces while explicitly exposing missing formal ORF inputs, missing attention evidence, and unavailable residue/PDB assertions. Supplementary robustness, external sanity-check, diversity-risk, expert-evaluation, domain-tool positioning, and cross-family audit analyses supported traceability, report quality, and conservative evidence handling, but also showed that stable Precision@K under query perturbation does not necessarily imply stable retrieved evidence sets. ViroBioTree operates offline and deterministically, but does not address raw-read assembly, base calling, primary ORF prediction, or wet-lab validation. Its results should be interpreted as proxy and expert-reviewed evidence for traceable viral protein evidence retrieval and report generation rather than as direct validation of biological function annotation.

16 June 2025 in International Journal of Financial Engineering
Verified
Journal Article
Closed access
JDJiale Du
Jiale Du
SLShuo Li
Shuo Li
FLFuguo Liu
Fuguo Liu
YSYufeng Shi
Yufeng Shi

21 May 2026 in Axioms
Verified
Journal Article
Open access
PDF file
JYJibin Yang
Jibin Yang
MTMaozai Tian
Maozai Tian
FLFuguo Liu
Fuguo Liu
Standard Bayesian autoregressive changepoint models can become unstable near sample boundaries. As a candidate changepoint approaches either edge of the series, the local residual degrees of freedom shrink, producing a Gamma-function singularity in the marginal likelihood that can strongly bias the posterior toward spurious edge detections. To address this issue, we introduce a regularization framework driven by local degrees of freedom. By incorporating a centripetal prior of the form π(k)∝(ν1ν2)λ—where ν1=k−2p−1 and ν2=n−k−p−1—the proposed method is designed to counteract this boundary effect. Theoretical analysis shows that a regularization intensity of λ≥1 is sufficient to offset this boundary effect asymptotically. Simulation results confirm that this approach substantially mitigates the U-shaped error profile typical of unregularized estimators, yielding a more favorable accuracy–robustness trade-off relative to the standard frequentist baselines considered in our study. Finally, empirical applications to several 2022 natural gas benchmarks, including TTF, SHPGX LNG, JKM, NBP, and NYMEX Henry Hub, demonstrate the framework’s ability to distinguish persistent structural transitions from transient market turbulence. These results suggest that degree-of-freedom-based centripetal prior regularization can improve the stability of Bayesian changepoint inference in nonstationary time series.