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Null allele allelic dropouts or rare sex detection in clonal organisms: simulations and application to real data sets of pathogenic microbes

机译:克隆生物中的无效等位基因等位基因缺失或罕见性别检测:模拟和应用于病原微生物的真实数据集

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摘要

BackgroundPathogens and their vectors are organisms whose ecology is often only accessible through population genetics tools based on spatio-temporal variability of molecular markers. However, molecular tools may present technical difficulties due to the masking of some alleles (allelic dropouts and/or null alleles), which tends to bias the estimation of heterozygosity and thus the inferences concerning the breeding system of the organism under study. This is especially critical in clonal organisms in which deviation from panmixia, as measured by Wright’s FIS, can, in principle, be used to infer both the extent of clonality and structure in a given population. In particular, null alleles and allelic dropouts are locus specific and likely produce high variance of Wright’s FIS across loci, as rare sex is expected to do. In this paper we propose a tool enabling to discriminate between consequences of these technical problems and those of rare sex.
机译:背景病原体及其载体是通常只能通过基于分子标记的时空变异的种群遗传学工具才能获得其生态的生物。然而,由于某些等位基因的掩盖(等位基因缺失和/或无效等位基因),分子工具可能会出现技术难题,这往往会影响杂合性的估计,从而使有关被研究生物的繁殖系统的推论产生偏差。这在克隆生物中尤为重要,在克隆生物中,根据赖特的FIS测量,与大猩猩的偏离可以从原理上推断出给定人群的克隆程度和结构。尤其是,无效的等位基因和等位基因缺失是特定于基因座的,并且可能会在整个基因座上产生赖特FIS的高度变异,这与稀有性行为一样。在本文中,我们提出了一种工具,可以区分这些技术问题的后果和稀有性行为的后果。

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