Dimitrov, N. | Search bioRxiv

bioRxiv2026

The effects of fox movement and landscape heterogeneity on the spread of sarcoptic mange in urban settings

ContextThe movement of vertebrate hosts across urbanized landscapes can play a key role in the transmission of direct-contact diseases. Understanding how wildlife hosts move in urban landscapes, and how transmission is affected by their landscape-constrained and disease-altered movements, is imperative for better predicting the spread of disease. ObjectiveWe assess how the movement of red foxes (Vulpes vulpes) according to landcover type, and their infection status, affect the spread of mange (caused by Sarcoptes scabiei) in an urbanized landscape. MethodsWe developed a mange transmission model (MTM) using an agent-based model to compare two movement behaviours of foxes in Scarborough (Ontario, Canada): random and landcover-based. We further assessed the effects of movement on disease transmission by considering the foxs infection status and comparing a range of movement probability scenarios. We quantified the number of effective contact events and the effective reproduction number (Re) according to each scenario. ResultsWe found that both landcover-dependent movement and infection status influenced the spread of mange within fox populations. The number of effective contact events and effective reproduction number Re was greatest when landscape heterogeneity was included in the model and foxes moved through paths of least resistance to movement, and when susceptible and infected foxes had an equal probability of leaving a fragmented habitat patch. ConclusionsOur findings suggest that mange spread may be accelerated along movement corridors in fragmented, heterogenous landscapes. As urban areas expand and remnant habitat within these is further lost and animals are relegated to fewer movement pathways, disease transmission may increase.

ecology↗

bioRxiv2024

The Genotype and Phenotypes in Families (GPF) platform manages the large and complex data at SFARI

The exploration of genotypic variants impacting phenotypes is a cornerstone in genetics research. The emergence of vast collections containing deeply genotyped and phenotyped families has made it possible to pursue the search for variants associated with complex diseases. However, managing these large-scale datasets requires specialized computational tools tailored to organize and analyze the extensive data. GPF (Genotypes and Phenotypes in Families) is an open-source platform (https://github.com/iossifovlab/gpf) that manages genotypes and phenotypes derived from collections of families. The GPF interface allows interactive exploration of genetic variants, enrichment analysis for de novo mutations, and phenotype/genotype association tools. In addition, GPF allows researchers to share their data securely with the broader scientific community. GPF is used to disseminate two large-scale family collection datasets (SSC, SPARK) for the study of autism funded by the SFARI foundation. However, GPF is versatile and can manage genotypic data from other small or large family collections. Our GPF-SFARI GPF instance (https://gpf.sfari.org/) provides protected access to comprehensive genotypic and phenotypic data for the SSC and SPARK. In addition, GPF-SFARI provides public access to an extensive collection of de novo mutations identified in individuals with autism and related disorders and to gene-level statistics of the protected datasets characterizing the genes roles in autism. Here, we highlight the primary features of GPF within the context of GPF-SFARI.

bioinformatics↗