Search bioRxiv⌕ Search

bioRxiv · 10.1101/407965

Bayesian coalescent inference of in-host evolution using Next Generation Sequencing

Abstract

Within an infected individual, influenza virus exists as a heterogeneous population of variants. When representing the viral population as a consensus sequence, information about minority variants is lost. However, using next generation sequencing (NGS), it is possible to identify nucleotide substitutions which segregate at low frequencies in the viral population, and can give insight into the within-host processes that drive the viruss evolution, and is a step towards understanding the dynamics of the disease. During the course of an infection, mutations may occur, and at each segregating site, the frequency of the derived allele in the population will fluctuate. We develop a method which can use information about the relative frequencies of mutations in NGS data from a viral population sampled at multiple time points, to infer past population dynamics with a Bayesian skyline model. By using coalescent theory, we analytically derive the joint allele frequency spectrum for a population across multiple time points, and relate this to the coalescent intervals generated from the skyline model. We demonstrate the model on data taken from populations of equine influenza virus sampled during an infection, and show that it is possible to infer a posterior distribution of effective viral population size through time. We also show how the model can be used to infer the probability that a mutation occurred within-host, as opposed to being an ancestral mutation which occurred prior to infection.\n\nAuthor SummaryWhen a host is infected by a virus, many particles of the infecting agent enter the body of the host. This viral population is composed of many closely related viruses that continue diversifying by mutating while reproducing in the host. New sequencing technologies allow the quantifying of the proportion of the different variants present in the host at a particular time. Unfortunately, the data resulting from such sequencing techniques are difficult to interpret as they consist of many unlinked copies of relatively small fragments of genetic code distributed along the genome of the virus.\n\nWe designed a method combining models of virus genealogies and frequency of mutations appearing in the data to reconstruct the variation of the viral population inside the host. It also allows us to time the apparition of particular variants. This could be useful to detect if a particular mutation (e.g. providing drug resistance) has appeared in host or was circulating before. We applied our method to data of within-host evolution of equine influenza.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Leen, G., Baguelin, M.. 2018-09-04. Bayesian coalescent inference of in-host evolution using Next Generation Sequencing. https://doi.org/10.1101/407965

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

KEEP EXPLORING

Related preprints

The Almond Expression Atlas: A comprehensive multi-tissue transcriptomic resource for almond gene expression

Background: Improving crop adaptation and enhancing agronomic and quality traits requires a deeper understanding of gene expression regulation, for which expression atlases are valuable tools. Almond (Prunus dulcis (Mill.) D.A. Webb) is one of the most economically important tree nut crops worldwide. However, an integrated transcriptomic resource for this species is still lacking. Available data remain fragmented across independent studies, limiting their comparability and reuse. Results: Here, we present the first almond gene expression atlas: a comprehensive multi-tissue transcriptomic resource integrating publicly available RNA sequencing data. A total of 142 high-quality untreated and control samples from 17 independent projects were curated through a metadata standardization process and analyzed using a unified bioinformatics pipeline. Standardized expression profiles were generated for 25,225 annotated genes in the Prunus dulcis Texas v2.0 reference genome. The atlas integrates two complementary expression approaches: a median TPM approach capturing quantitative expression levels and a rank-based strategy implemented using the Bgee expression calling method, designed to improve comparability across heterogeneous datasets. This design enables the identification of tissue-specific candidate genes and the exploration of expression patterns across tissues and developmental stages. Its applicability is demonstrated through two use cases, highlighting its ability to identify biologically meaningful gene sets associated with bud dormancy transitions and to prioritize candidate reference genes for RT-qPCR normalization in almond. Conclusions: The Almond Expression Atlas v1.0 is publicly available through FruitDBase (fruitdbase.csic.es), providing an interactive platform for gene expression exploration and visualization. This resource supports functional genomics studies and facilitates candidate gene discovery in almond, while ensuring data traceability and promoting data reusability.

bioinformatics↗

Leakage-Controlled Benchmarking of Variant Effect Predictors and Development of Gradient-Boosting Consensus Model

Single amino acid mutations are among the most common forms of genetic variation, with effects ranging from negligible to severe disruption of protein function. Accurate quantitative evaluation of protein variants therefore represents a key challenge in medicine and protein engineering. Computational variant effect predictors (VEPs) are widely used to prioritize missense variants, yet their fair comparison is hindered by data circularity, benchmarks restricted to human clinical annotations, and limited availability of code and training data, all of which can inflate apparent performance. Here, we reviewed 18 recent and 3 older, widely adopted variant effect predictors for reproducible benchmarking and assembled a rigorously curated, leakage-controlled Benchmark dataset by integrating clinically annotated human variants from ClinVar and Humsavar as well as cross-species variants with functional annotations. The evaluation on this dataset revealed a narrow overall performance range for the benchmarked tools (AUC 0.631-0.758) and a consistent drop from clinical to functional data. Surprisingly, several tools published two decades ago demonstrated comparable performance to mid-ranked modern predictors. Building on these results, we developed a gradient-boosting consensus model, PredictSNPprot, which achieved an AUC of 0.82 on a held-out test set, outperforming the original PredictSNP meta-predictor and the best individual state-of-the-art tool by 13.6 and 5.7 percentage points, respectively. The Benchmark dataset, including the predictions from the evaluated tools, is available at https://doi.org/10.5281/zenodo.23597130 and PredictSNPprot consensus predictor is available at https://github.com/loschmidt/PredictSNPprot.

bioinformatics↗

MaCADEMIA: a software toolbox for single-molecule fluorescence image quantification

Single-molecule localisation microscopy (SMLM) is a powerful tool in molecular and cellular biology and part of the broad umbrella of super-resolution microscopy. A distinct feature of SMLM, is its capacity for deep quantification, beyond just spatial information, to copy number, stoichiometry, molecular interaction and dynamics in living cells. The hardware required is increasingly straightforward to implement. However, complexity remains in the image analysis where much remains fragmented across specialised software tools. Here, we present MaCADEMIA (Matlab Computational Analysis of Diffusion, Emitter Molecular Intensity and Abundance), a simple yet powerful toolbox of MATLAB functions and associated documentation to enable straightforward extraction of quantitative single-molecule information. MaCADEMIA performs ensemble particle detection achieving localisation accuracies down to 0.5 pixels Root mean squared error (RMSE) across wide signal-to-noise (SNR) ranges on standardised particle tracking benchmarks, consistently matching or exceeding the performance of 14 leading methods. Our integrated workflow enables molecular counting and stoichiometry determination through stepwise photobleaching analysis, mobility measurement via mean squared displacement, colocalisaton analysis and absolute protein copy number quantification using three-dimensional cellular models.

bioinformatics↗