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A Novel Software and Method for the Efficient Development of Polymorphic SSR Loci Based on Transcriptome Data

机译:基于转录组数据的多态SSR基因座高效开发新软件和方法

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摘要

Traditional methods for developing polymorphic microsatellite loci without reference sequences are time-consuming and labor-intensive, and the polymorphisms of simple sequence repeat (SSR) loci developed from expressed sequence tag (EST) databases are generally poor. To address this issue, in this study, we developed a new software (PSSRdt) and established an effective method for directly obtaining polymorphism details of SSR loci by analyzing diverse transcriptome data. The new method includes three steps, raw data processing, PSSRdt application, and loci extraction and verification. To test the practicality of the method, we successfully obtained 1940 potential polymorphic SSRs from the transcript dataset combined with 44 pea aphid transcriptomes. Fifty-two SSR loci obtained by the new method were selected for validating the polymorphic characteristics by genotyping in pea aphid individuals. The results showed that over 92% of SSR loci were polymorphic and 73.1% of loci were highly polymorphic. Our new software and method provide an innovative approach to microsatellite development based on RNA-seq data, and open a new path for the rapid mining of numerous loci with polymorphism to add to the body of research on microsatellites.
机译:在没有参考序列的情况下开发多态微卫星基因座的传统方法既耗时又费力,并且从表达序列标签(EST)数据库开发的简单序列重复(SSR)基因座的多态性通常较差。为了解决这个问题,在本研究中,我们开发了一个新软件(PSSRdt),并建立了一种通过分析各种转录组数据直接获取SSR基因座多态性细节的有效方法。新方法包括三个步骤:原始数据处理,PSSRdt应用以及位点提取和验证。为了测试该方法的实用性,我们成功地从转录数据集中结合了44个豌豆蚜转录组,获得了1940个潜在的多态性SSR。选择通过新方法获得的52个SSR基因座,通过豌豆蚜虫个体的基因分型来验证其多态性。结果表明,超过92%的SSR位点是多态的,而73.1%的基因座是高度多态的。我们的新软件和方法为基于RNA-seq数据的微卫星开发提供了创新的方法,并为快速挖掘具有多态性的众多基因座增加了微卫星研究的基础开辟了一条新途径。

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