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Biology subjects

Rayan, S.

Publications and source records attributed to Rayan, S..

2 recordsLinked to original sources

Quantum-Classical Reservoir Computing to Predict Influenza H3N2 Antigenic Distance

Accurate prediction of antigenic distance between influenza A/H3N2 strains is essential for timely vaccine strain selection, yet traditional hemagglutination inhibition (HI) assays are labour-intensive and limited in throughput. We present FluQRC, a hybrid Quantum-Classical Reservoir Computing framework for sequence-based antigenic distance prediction. FluQRC integrates three novel components: (1) a differentiable gated property ranking network for data-driven property selection, (2) a dimensionality reduction network that compresses the feature representation into a form suitable for quantum processing, and (3) a hybrid quantum-classical reservoir computing architecture for antigenic distance prediction. Experiments on two datasets covering 1963-2002 (271 strains, 73,441 pairs) and 2003-2025 (888 strains, 788,544 pairs) show that FluQRC outperforms four established baselines across all three evaluation metrics (MAE, RMSE, R2). On the larger and more challenging 2003-2025 dataset, FluQRC achieves MAE = 0.369, RMSE = 0.635, and R2 = 0.900, corresponding to a 20.3% reduction in MAE and a 14.3% reduction in RMSE relative to the strongest baseline, while raising R2 from 0.862 to 0.900. These results demonstrate the scalability and effectiveness of FluQRC for large-scale antigenic distance prediction.

bioinformatics↗

Explaining the pathogenesis of African swine fever using knowledge-driven regulatory network modeling

A lethal DNA virus with significant economic impact on livestock farmers worldwide, the pathogenesis of African swine fever virus (ASFV) infection is complex and continues to challenge the development of effective vaccine candidates. The requirement for high-containment conditions further complicates its study, resulting in limitations in sample size and marker assessment that challenge conventional statistical analysis. In this work we demonstrate how prior knowledge of immune biology and pathogen-host proteome interactions can be leveraged and reconciled with sparse experimental data to deliver plausible mechanistically informed hypotheses describing ASFV illness progression. We apply large-scale automated mining of literature and pathway schema together with generative artificial intelligence (AI) to create closed-loop regulatory network models consisting of 133 pathogen and host proteins linked by 676 regulatory interactions. Immune regulatory tuning of these networks is reverse engineered to explain two distinct experimentally observed illness progression trajectories in only 5 markers measured every second day over a maximum of 8 days. Comparison of network model pools specific to each progression phenotype suggest that these significantly different outcomes may arise from altered regulatory tuning of genes coding for interleukin (IL)1{beta}, tumor necrosis factor (TNF) and Forkhead box protein (FOX)O4, potentially as a result of epigenetic adaptations. Simulated challenges with individual ASFV protein confirm broadly delayed interferon (IFN)-{gamma}I response in both phenotypes, with multigene family (MGF)505-3R offering the earliest induction and only in the more severe phenotype. Paradoxically, predictions suggest that this delay is preceded by an early IL-10 induction by this same viral protein. While added model granularity and validation is needed, we propose that this proof-of-concept knowledge driven approach offers an attractive solution to mechanistic hypothesis generation in data poor environments.

Systems Biology↗