Original Article

Heredity (2004) 93, 504–509. doi:10.1038/sj.hdy.6800545 Published online 4 August 2004

Microsatellite null alleles in parentage analysis

E E Dakin1 and J C Avise1

1Department of Genetics, University of Georgia, Athens, GA 30602, USA

Correspondence: EE Dakin, Department of Genetics, University of Georgia, Athens, GA 30602, USA. E-mail: elmccoy@uga.edu

Received 29 January 2004; Accepted 20 May 2004; Published online 4 August 2004.

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Abstract

Highly polymorphic microsatellite markers are widely employed in population genetic analyses (eg, of biological parentage and mating systems), but one potential drawback is the presence of null alleles that fail to amplify to detected levels in the PCR assays. Here we examine 233 published articles in which authors reported the suspected presence of one or more microsatellite null alleles, and we review how these purported nulls were detected and handled in the data analyses. We also employ computer simulations and analytical treatments to determine how microsatellite null alleles might impact molecular parentage analyses. The results indicate that whereas null alleles in frequencies typically reported in the literature introduce rather inconsequential biases on average exclusion probabilities, they can introduce substantial errors into empirical assessments of specific mating events by leading to high frequencies of false parentage exclusions.

Keywords:

exclusion probability, parentage, population genetics, nonamplifying alleles

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