Evaluating mixed samples as a source of error in non-invasive genetic studies using microsatellites
Article first published online: 19 NOV 2004
DOI: 10.1111/j.1365-294X.2004.02385.x
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How to Cite
ROON, D. A., THOMAS, M. E., KENDALL, K. C. and WAITS, L. P. (2005), Evaluating mixed samples as a source of error in non-invasive genetic studies using microsatellites. Molecular Ecology, 14: 195–201. doi: 10.1111/j.1365-294X.2004.02385.x
Publication History
- Issue published online: 19 NOV 2004
- Article first published online: 19 NOV 2004
- Received 30 June 2004; revision received 22 September 2004; accepted 22 September 2004
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Keywords:
- genotype error;
- individual identification;
- mark-recapture;
- microsatellites;
- noninvasive genetic sampling;
- Ursus arctos
Abstract
The use of noninvasive genetic sampling (NGS) for surveying wild populations is increasing rapidly. Currently, only a limited number of studies have evaluated potential biases associated with NGS. This paper evaluates the potential errors associated with analysing mixed samples drawn from multiple animals. Most NGS studies assume that mixed samples will be identified and removed during the genotyping process. We evaluated this assumption by creating 128 mixed samples of extracted DNA from brown bear (Ursus arctos) hair samples. These mixed samples were genotyped and screened for errors at six microsatellite loci according to protocols consistent with those used in other NGS studies. Five mixed samples produced acceptable genotypes after the first screening. However, all mixed samples produced multiple alleles at one or more loci, amplified as only one of the source samples, or yielded inconsistent electropherograms by the final stage of the error-checking process. These processes could potentially reduce the number of individuals observed in NGS studies, but errors should be conservative within demographic estimates. Researchers should be aware of the potential for mixed samples and carefully design gel analysis criteria and error checking protocols to detect mixed samples.

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