ArticleG3 (Bethesda, Md.)2015
How Well Do Molecular and Pedigree Relatedness Correspond, in Populations with Diverse Mating Systems, and Various Types and Quantities of Molecular and Demographic Data?
Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Relatedness of White-Tailed Deer from Culling Efforts Within Chronic Wasting Disease Management Zones in Minnesota.Pathogens (Basel, Switzerland) · 2025Article
- Parental kinship coefficient but not paternal coloration predicts early offspring growth in lake char.Heredity · 2024Article
- Pedigree reconstruction and population structure using SNP markers in Gir cattle.Journal of applied genetics · 2023Article
- Fitness benefits of male dominance behaviours depend on the degree of individual inbreeding in a polyandrous lizard.Proceedings. Biological sciences · 2020Article
- From microsatellites to single nucleotide polymorphisms for the genetic monitoring of a critically endangered sturgeon.Ecology and evolution · 2019Article
- PopPAnTe: population and pedigree association testing for quantitative data.BMC genomics · 2017Article
- Strategies for determining kinship in wild populations using genetic data.Ecology and evolution · 2016Review
- Estimating population size using single-nucleotide polymorphism-based pedigree data.Ecology and evolution · 2016Article
Corrections and comments
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Authors and funding
4 authors.
Funding
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Abstract
Kinship analyses are important pillars of ecological and conservation genetic studies with potentially far-reaching implications. There is a need for power analyses that address a range of possible relationships. Nevertheless, such analyses are rarely applied, and studies that use genetic-data-based-kinship inference often ignore the influence of intrinsic population characteristics. We investigated 11 questions regarding the correct classification rate of dyads to relatedness categories (relatedness category assignments; RCA) using an individual-based model with realistic life history parameters. We investigated the effects of the number of genetic markers; marker type (microsatellite, single nucleotide polymorphism SNP, or both); minor allele frequency; typing error; mating system; and the number of overlapping generations under different demographic conditions. We found that (i) an increasing number of genetic markers increased the correct classification rate of the RCA so that up to >80% first cousins can be correctly assigned; (ii) the minimum number of genetic markers required for assignments with 80 and 95% correct classifications differed between relatedness categories, mating systems, and the number of overlapping generations; (iii) the correct classification rate was improved by adding additional relatedness categories and age and mitochondrial DNA data; and (iv) a combination of microsatellite and single-nucleotide polymorphism data increased the correct classification rate if <800 SNP loci were available. This study shows how intrinsic population characteristics, such as mating system and the number of overlapping generations, life history traits, and genetic marker characteristics, can influence the correct classification rate of an RCA study. Therefore, species-specific power analyses are essential for empirical studies.
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