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Consistent Reanalysis of Genome-wide Imprinting Studies in Plants Using Generalized Linear Models Increases Concordance across Datasets

机译:使用广义线性模型对植物中全基因组印迹研究进行一致的再分析可提高数据集之间的一致性

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摘要

Genomic imprinting leads to different expression levels of maternally and paternally derived alleles. Over the last years, major progress has been made in identifying novel imprinted candidate genes in plants, owing to affordable next-generation sequencing technologies. However, reports on sequencing the transcriptome of hybrid F1 seed tissues strongly disagree about how many and which genes are imprinted. This raises questions about the relative impact of biological, environmental, technical, and analytic differences or biases. Here, we adopt a statistical approach, frequently used in RNA-seq data analysis, which properly models count overdispersion and considers replicate information of reciprocal crosses. We show that our statistical pipeline outperforms other methods in identifying imprinted genes in simulated and real data. Accordingly, reanalysis of genome-wide imprinting studies in Arabidopsis and maize shows that, at least for Arabidopsis, an increased agreement across datasets could be observed. For maize, however, consistent reanalysis did not yield a larger overlap between the datasets. This suggests that the discrepancy across publications might be partially due to different analysis pipelines but that technical, biological, and environmental factors underlie much of the discrepancy between datasets. Finally, we show that the set of genes that can be characterized regarding allelic bias by all studies with minimal confidence is small (~8,000/27,416 genes for Arabidopsis and ~12,000/39,469 for maize). In conclusion, we propose to use biologically replicated reciprocal crosses, high sequence coverage, and a generalized linear model approach to identify differentially expressed alleles in developing seeds.
机译:基因组印迹导致母本和父本等位基因的不同表达水平。在过去的几年中,由于负担得起的下一代测序技术,在鉴定植物中新的印迹候选基因方面取得了重大进展。但是,有关杂交F1种子组织转录组测序的报道强烈反对印记多少基因和哪些基因。这就提出了有关生物学,环境,技术和分析差异或偏见的相对影响的问题。在这里,我们采用一种统计方法,通常用于RNA序列数据分析中,该方法可以正确地对计数过度分散进行建模,并考虑相互交叉的重复信息。我们证明了我们的统计渠道在识别模拟和真实数据中的印迹基因方面优于其他方法。因此,对拟南芥和玉米中全基因组印迹研究的重新分析表明,至少对于拟南芥,可以观察到整个数据集之间一致性的提高。但是,对于玉米而言,一致的再分析并未在数据集之间产生较大的重叠。这表明出版物之间的差异可能部分是由于不同的分析渠道造成的,但是技术,生物学和环境因素是数据集之间差异的主要原因。最后,我们显示所有研究都可以以最小的置信度来表征等位基因偏倚的基因集很小(拟南芥约为8,000 / 27,416,玉米约为12,000 / 39,469)。总之,我们建议使用生物复制的反向杂交,高序列覆盖率和广义线性模型方法来鉴定发育中种子中差异表达的等位基因。

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