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Genotyping by Amplicon Sequencing (GBAS) With Newly Developed SSR and EPIC Markers Reveals Structure in Populations of the Green Toad (Bufotes viridis) Across Rural and Urban Environments
Genotyping by Amplicon Sequencing (GBAS) With Newly Developed SSR and EPIC Markers Reveals Structure in Populations of the Green Toad (Bufotes viridis) Across Rural and Urban Environments
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Genotyping by Amplicon Sequencing (GBAS) With Newly Developed SSR and EPIC Markers Reveals Structure in Populations of the Green Toad (Bufotes viridis) Across Rural and Urban Environments
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Genotyping by Amplicon Sequencing (GBAS) With Newly Developed SSR and EPIC Markers Reveals Structure in Populations of the Green Toad (Bufotes viridis) Across Rural and Urban Environments
Genotyping by Amplicon Sequencing (GBAS) With Newly Developed SSR and EPIC Markers Reveals Structure in Populations of the Green Toad (Bufotes viridis) Across Rural and Urban Environments

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Genotyping by Amplicon Sequencing (GBAS) With Newly Developed SSR and EPIC Markers Reveals Structure in Populations of the Green Toad (Bufotes viridis) Across Rural and Urban Environments
Genotyping by Amplicon Sequencing (GBAS) With Newly Developed SSR and EPIC Markers Reveals Structure in Populations of the Green Toad (Bufotes viridis) Across Rural and Urban Environments
Journal Article

Genotyping by Amplicon Sequencing (GBAS) With Newly Developed SSR and EPIC Markers Reveals Structure in Populations of the Green Toad (Bufotes viridis) Across Rural and Urban Environments

2025
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Overview
ABSTRACT Microsatellites (SSRs) are reliable markers for population genetic analyses but often suffer from null alleles caused by mutations in primer binding sites. Exon‐primed intron‐crossing (EPIC) markers address these limitations and serve as a complementary tool. In this study, we developed SSR and EPIC markers for the green toad (Bufotes viridis). We demonstrated their effectiveness using genotyping by high‐throughput amplicon sequencing (GBAS) across urban and rural populations. Marker development followed an established in‐house protocol. We then tested their functionality in singleplex‐PCRs before employing them in multiplex reactions and preparing them for sequencing. We analyzed the resulting data using several variability measures as well as individual‐based clustering methods. From the initial set of 48 markers of each type, 35 SSR and 46 EPIC markers consistently amplified across samples both in singleplex and multiplex assays. Data analysis did not corroborate the expectation of a continuous reduction of diversity in urban populations compared to rural ones. Clustering methods using EPIC markers revealed ecologically coherent results, showing weaker genetic structure in rural environments, whereas the SSRs' signal reflected drift‐induced patterns. Our findings suggest that the green toad exhibits a degree of resilience to urban environments. Furthermore, EPIC markers not only complement SSRs by having fewer null alleles but also provide greater robustness to random drift events. We recommend their combined use, especially in fragmented environments prone to genetic drift, such as urban areas. We developed and tested SSR and EPIC markers for the green toad (Bufotes viridis), demonstrating their effectiveness using genotyping by high‐throughput amplicon sequencing (GBAS) across urban and rural populations. EPIC markers exhibited fewer null alleles and provided more ecologically coherent clustering results, while SSRs reflected drift‐induced patterns. Our findings indicate that B. viridis may retain genetic diversity in urban environments and highlight the value of combining EPIC and SSR markers, particularly in fragmented habitats prone to genetic drift.