4.7 Article

Evaluating sample size to estimate genetic management metrics in the genomics era

Journal

MOLECULAR ECOLOGY RESOURCES
Volume 18, Issue 5, Pages 1077-1091

Publisher

WILEY
DOI: 10.1111/1755-0998.12898

Keywords

kinship; Ovis canadensis canadensis; sampling; single nucleotide polymorphism

Funding

  1. Montana Fish, Wildlife and Parks
  2. Glacier National Park
  3. Yellowstone National Park
  4. National Science Foundation
  5. Montana Chapter of the Wild Sheep Foundation
  6. Midwest Chapter of the Wild Sheep Foundation
  7. National Geographic Society
  8. University of Wyoming
  9. Montana Agricultural Experiment Station
  10. Canon USA Inc.
  11. Wyoming Governor's Big Game License Coalition
  12. National Park Service
  13. U.S. Geological Survey

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Inbreeding and relationship metrics among and within populations are useful measures for genetic management of wild populations, but accuracy and precision of estimates can be influenced by the number of individual genotypes analysed. Biologists are confronted with varied advice regarding the sample size necessary for reliable estimates when using genomic tools. We developed a simulation framework to identify the optimal sample size for three widely used metrics to enable quantification of expected variance and relative bias of estimates and a comparison of results among populations. We applied this approach to analyse empirical genomic data for 30 individuals from each of four different free-ranging Rocky Mountain bighorn sheep (Ovis canadensis canadensis) populations in Montana and Wyoming, USA, through cross-species application of an Ovine array and analysis of approximately 14,000 single nucleotide polymorphisms (SNPs) after filtering. We examined intra- and interpopulation relationships using kinship and identity by state metrics, as well as F-ST between populations. By evaluating our simulation results, we concluded that a sample size of 25 was adequate for assessing these metrics using the Ovine array to genotype Rocky Mountain bighorn sheep herds. However, we conclude that a universal sample size rule may not be able to sufficiently address the complexities that impact genomic kinship and inbreeding estimates. Thus, we recommend that a pilot study and sample size simulation using R code we developed that includes empirical genotypes from a subset of populations of interest would be an effectiveapproach to ensure rigour in estimating genomic kinship and population differentiation.

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