Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.02.24.639875

Phylogenetic discordance cannot identify genomic reassortment events: a case study with the avian influenza virus H5Nx

Abstract

Recombination plays an important role in the evolution of RNA viruses, as it allows the exchange of genetic material between viral lineages. Reassortment, a form of recombination specific to segmented genomes, involves the exchange of entire segments and has contributed significantly to the adaptation and spread of influenza viruses through novel genomic combinations, i.e., antigenic shifts. It is usually identified by phylogenetic discordance: differences in the topologies of trees reconstructed from different genomic segments. However, phylogenetic discordance can also result from error in reconstructing trees. To characterize the impact of reconstruction error, we curated a database of n = 11, 765 complete genomes of avian H5Nx influenza A viruses from avian hosts. We found evidence of widespread reassortment as measured by inferred subtree-prune-regraft (SPR) events, consistent with previous studies. Next, we ran replicate simulations of sequence evolution along the reference tree for the segment encoding hemagglutinin (HA), adjusting simulations for the lengths and clock rates of the other segments. These simulations provided a baseline for the expected amount of phylogenetic discordance in the absence of any reassortment. When sampling HA sequences at random from the database to build reference trees, we observed that simulating other segments without reassortment still yielded about 32% as many SPRs as the real segment data on average. The average proportion of SPRs without reassortment was greatly reduced (4%) if we selected an equivalent number of HA sequences retaining the most genetic diversity, which was consistent with the accuracy of phylogenetic reconstruction being the limiting factor. This implies that measuring reassortment by SPRs may have a high false positive rate, and that previous evidence of extensive reassortment in influenza viruses should be interpreted with caution. In addition, we observed that the SPRs reconstructed on simulated trees had significantly shorter distances between the prune and regraft locations than real trees. These results suggest that down-sampling sequences to maximize evolutionary divergence and filtering out the shortest SPRs may be effective measures against false positives.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Castelan-Sanchez, H., Poon, A.. 2025-02-28. Phylogenetic discordance cannot identify genomic reassortment events: a case study with the avian influenza virus H5Nx. https://doi.org/10.1101/2025.02.24.639875

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

deepTools4: Faster, Scalable, and Modernized Genomic Data Analysis

The deepTools suite is widely used for quality control, summarization, and visualization of high-throughput sequencing data. However, as genomic datasets grow in scale and depth, existing tools often become computational bottlenecks. We present deepTools4, a modernized framework designed for high performance, scalability, and enhanced usability, while maintaining seamless integration with the Galaxy platform. Core functionality has been rewritten and thoroughly benchmarked, achieving substantial computational speed-ups. Visualization tools have been modernized to provide more intuitive, high-quality graphical outputs. In addition, our testing framework has been expanded to facilitate continuous development and ensure robustness. We demonstrate the utility of deepTools4 across diverse epigenomics and transcriptomics datasets, highlighting its ability to summarize genome-wide signals, apply a wide range of common normalization methods, and visualize enrichment patterns. The enhanced deepTools4 framework delivers a faster, more scalable solution for reproducible genome-wide analysis and interpretation across many sequencing modalities. Availability: https://github.com/deeptools/deepTools/

bioinformatics↗

Reproducibility and cross-dataset concordance of drug-induced transcriptional responses

Drug-perturbation transcriptomic resources are expanding, but the reproducibility and cross-source consistency of the responses they measure remain critical to their use. We compared six resources using independent replicates, matched-drug analyses, and response decomposition. High agreement in treated expression did not translate into equally repeatable drug-induced changes. Cross-source response concordance was generally limited, including under matched cell and treatment conditions, although some comparisons retained drug-specific information. In Tahoe, a control-expression-only baseline left substantial drug-specific variation unresolved. Measured drug main effects - the average responses across cell lines - provided information for predicting cell-specific interactions, with this relationship retained in a cross-plate validation. Exploratory analyses of structure, target, and external-response representations identified modest signals in selected pipelines. Together, these analyses characterize the reliability and transferability of current perturbation resources and identify prediction of drug main effects as a key bottleneck in the framework examined, motivating shared reference measurements and better recovery of drug-specific responses.

bioinformatics↗

Propensity-Adjusted AUC under Nuisance-Model Misspecification

Propensity adjustment compares medical-image detector scores within groups with similar measured properties, such as stain or focus. We examine its sensitivity to the nuisance model that forms those groups. Under Gaussian latent-index assumptions and exact linear-index strata, a closed-form correlation gives an exact boundary for adjusted AUC to fall below one half. Quadrature matches 36 simulation cells within 0.008. Inflation and attenuation relative to correct adjustment are empirical findings, not general ordering results. An overlap screen and a self-stratified control introduced for this study miss 140 of 141 simulated cells with absolute error above 0.05: checking the fitted propensity cannot certify completeness of the adjustment set. On real pathology corpora, logistic and boosted-tree models using the same 16 features disagree. Among splits where both pass both checks, mean adjusted-AUC gaps are 0.057 on acid-fast bacilli (AFB), 0.048 on Kaggle, and 0.049 on PCam, over three, five, and three splits respectively. These gaps measure model sensitivity; neither estimate is known to be correct. A controlled colour shift moves adjusted AUC relative to model-specific references in the predicted direction in 78 of 80 label-dependent cells. Broader balance and label-fit diagnostics favour trees without certifying their adjusted AUC. We recommend reporting sensitivity across nuisance models alongside these diagnostics. Reversal relative to known truth occurs in constructed stress tests; its frequency in practice remains unknown.

bioinformatics↗