| Literature DB >> 31925943 |
Alina von Thaden1,2, Carsten Nowak1,3, Annika Tiesmeyer1,2, Tobias E Reiners1,2, Paulo C Alves4,5,6, Leslie A Lyons7, Federica Mattucci8, Ettore Randi9,10, Margherita Cragnolini11, José Galián12, Zsolt Hegyeli13, Andrew C Kitchener14,15, Clotilde Lambinet16, José M Lucas12, Thomas Mölich17, Luana Ramos4,5, Vinciane Schockert16, Berardino Cocchiararo1,3.
Abstract
The genomic era has led to an unprecedented increase in the availability of genome-wide data for a broad range of taxa. Wildlife management strives to make use of these vast resources to enable refined genetic assessments that enhance biodiversity conservation. However, as new genomic platforms emerge, problems remain in adapting the usually complex approaches for genotyping of noninvasively collected wildlife samples. Here, we provide practical guidelines for the standardized development of reduced single nucleotide polymorphism (SNP) panels applicable for microfluidic genotyping of degraded DNA samples, such as faeces or hairs. We demonstrate how microfluidic SNP panels can be optimized to efficiently monitor European wildcat (Felis silvestris S.) populations. We show how panels can be set up in a modular fashion to accommodate informative markers for relevant population genetics questions, such as individual identification, hybridization assessment and the detection of population structure. We discuss various aspects regarding the implementation of reduced SNP panels and provide a framework that will allow both molecular ecologists and practitioners to help bridge the gap between genomics and applied wildlife conservation.Entities:
Keywords: zzm321990Felis silvestriszzm321990; conservation biology; degraded DNA; genetic noninvasive sampling; reduced SNP panel; wildlife genomics
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Year: 2020 PMID: 31925943 PMCID: PMC7199164 DOI: 10.1111/1755-0998.13136
Source DB: PubMed Journal: Mol Ecol Resour ISSN: 1755-098X Impact factor: 7.090