Richard Annan | Searcharxiv

arXiv2026

Inferring and Predicting Clade-Level Relative Transmission Fitness in Seasonal Influenza A Using Differential Population Growth Rate and Deep Learning

Seasonal influenza A evolves rapidly, allowing newly emerged clades to replace previously dominant lineages and complicate surveillance and vaccine evaluation. Here, we applied the Differential Population Growth Rate (DPGR) framework to GISAID-derived H3N2 and H1N1 surveillance data collected from 1 January 2014 to 12 February 2026, including the 2025-2026 influenza season, to estimate clade-level relative transmission fitness across continents and within the United States. We identified windows of co-circulation with sliding-window regression, reconstructed relative-fitness relationships among clades, and compared inferred growth advantages with independent WHO and CDC surveillance patterns. We further trained subtype-specific convolutional neural networks on complete viral genomes to predict DPGR from sequence, quantified predictive uncertainty with conformal prediction, and used SHAP to localize genomic contributors to fitness. DPGR recovered recurrent lineage turnover in both subtypes and consistently identified the emerging H3N2 subclade K as fitter than the 2025-2026 vaccine-lineage background across multiple regions. Genome-based models predicted DPGR accurately for H3N2 ($R^2 = 0.9577$) and H1N1 ($R^2 = 0.9871$), while interpretation highlighted known haemagglutinin antigenic sites together with contributions from internal genes. These results support DPGR as an interpretable surveillance signal and show that influenza fitness can be linked to genomic prediction and biological interpretation in a unified framework.

q-bio.PE↗

arXiv2024

Explainable convolutional neural network model provides an alternative genome-wide association perspective on mutations in SARS-CoV-2

Identifying mutations of SARS-CoV-2 strains associated with their phenotypic changes is critical for pandemic prediction and prevention. We compared an explainable convolutional neural network (CNN) approach and the traditional genome-wide association study (GWAS) on the mutations associated with WHO labels of SARS-CoV-2, a proxy for virulence phenotypes. We trained a CNN classification model that can predict genomic sequences into Variants of Concern (VOCs) and then applied Shapley Additive explanations (SHAP) model to identify mutations that are important for the correct predictions. For comparison, we performed traditional GWAS to identify mutations associated with VOCs. Comparison of the two approaches shows that the explainable neural network approach can more effectively reveal known nucleotide substitutions associated with VOCs, such as those in the spike gene regions. Our results suggest that explainable neural networks for genomic sequences offer a promising alternative to the traditional genome wide analysis approaches.

q-bio.GN↗