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High-Resolution Genotyping via Whole Genome Hybridizations to Microarrays Containing Long Oligonucleotide Probes

机译:通过全基因组杂交到包含长寡核苷酸探针的微阵列的高分辨率基因分型。

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摘要

To date, microarray-based genotyping of large, complex plant genomes has been complicated by the need to perform genome complexity reduction to obtain sufficiently strong hybridization signals. Genome complexity reduction techniques are, however, tedious and can introduce unwanted variables into genotyping assays. Here, we report a microarray-based genotyping technology for complex genomes (such as the 2.3 GB maize genome) that does not require genome complexity reduction prior to hybridization. Approximately 200,000 long oligonucleotide probes were identified as being polymorphic between the inbred parents of a mapping population and used to genotype two recombinant inbred lines. While multiple hybridization replicates provided ∼97% accuracy, even a single replicate provided ∼95% accuracy. Genotyping accuracy was further increased to >99% by utilizing information from adjacent probes. This microarray-based method provides a simple, high-density genotyping approach for large, complex genomes.
机译:迄今为止,由于需要进行基因组复杂性降低以获得足够强的杂交信号,因此复杂的大型植物基因组的基于微阵列的基因分型变得复杂。然而,基因组复杂性降低技术是乏味的,并且可以将不需要的变量引入基因分型测定中。在这里,我们报告了一种用于复杂基因组(例如2.3 GB玉米基因组)的基于微阵列的基因分型技术,该技术不需要在杂交前降低基因组复杂性。鉴定出约200,000长的寡核苷酸探针在作图群体的近交亲本之间是多态性的,并用于对两个重组近交系进行基因分型。尽管多次杂交重复提供了约97%的准确度,但即使是一次重复提供了约95%的准确度。利用来自相邻探针的信息,基因分型准确性进一步提高到> 99%。这种基于微阵列的方法为大型,复杂的基因组提供了一种简单的高密度基因分型方法。

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