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Population-wide sampling of retrotransposon insertion polymorphisms using deep sequencing and efficient detection

机译:使用深度测序和有效检测对反转录转座子插入多态性进行全人群采样

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Active retrotransposons play important roles during evolution and continue to shape our genomes today, especially in genetic polymorphisms underlying a diverse set of diseases. However, studies of human retrotransposon insertion polymorphisms (RIPs) based on whole-genome deep sequencing at the population level have not been sufficiently undertaken, despite the obvious need for a thorough characterization of RIPs in the general population. Herein, we present a novel and efficient computational tool called Specific Insertions Detector (SID) for the detection of non-reference RIPs. We demonstrate that SID is suitable for high-depth whole-genome sequencing data using paired-end reads obtained from simulated and real datasets. We construct a comprehensive RIP database using a large population of 90 Han Chinese individuals with a mean ×68 depth per individual. In total, we identify 9342 recent RIPs, and 8433 of these RIPs are novel compared with dbRIP, including 5826 Alu, 2169 long interspersed nuclear element 1 (L1), 383 SVA, and 55 long terminal repeats. Among the 9342 RIPs, 4828 were located in gene regions and 5 were located in protein-coding regions. We demonstrate that RIPs can, in principle, be an informative resource to perform population evolution and phylogenetic analyses. Taking the demographic effects into account, we identify a weak negative selection on SVA and L1 but an approximately neutral selection for Alu elements based on the frequency spectrum of RIPs. SID is a powerful open-source program for the detection of non-reference RIPs. We built a non-reference RIP dataset that greatly enhanced the diversity of RIPs detected in the general population, and it should be invaluable to researchers interested in many aspects of human evolution, genetics, and disease. As a proof of concept, we demonstrate that the RIPs can be used as biomarkers in a similar way as single nucleotide polymorphisms.
机译:活跃的反转录转座子在进化过程中发挥着重要作用,并在当今不断塑造着我们的基因组,特别是在多种疾病的遗传多态性中。然而,尽管显然需要在一般人群中对RIPs进行全面的表征,但在人群水平上基于全基因组深度测序的人类逆转录转座子插入多态性(RIPs)的研究尚未得到充分开展。在这里,我们提出了一种新颖且有效的计算工具,称为“特定插入检测器”(SID),用于检测非参考RIP。我们证明了SID适用于从模拟和真实数据集中获得的配对末端读取的深度全基因组测序数据。我们使用90名汉族人口构成的综合RIP数据库,每人平均×68深度。总的来说,我们确定了9342个最近的RIP,其中的8433个与dbRIP相比是新颖的,包括5826个Alu,2169个长穿插的核元件1(L1),383个SVA和55个长末端重复序列。在9342个RIP中,有4828个位于基因区域,有5个位于蛋白质编码区域。我们证明,RIPs原则上可以成为进行种群进化和系统发育分析的信息资源。考虑到人口统计学的影响,我们根据RIP的频谱确定了SVA和L1的较弱负选择,但对Alu元素却选择了中性选择。 SID是用于检测非参考RIP的功能强大的开源程序。我们建立了一个非参考RIP数据集,该数据集大大增强了普通人群中检测到的RIP的多样性,对于对人类进化,遗传学和疾病的许多方面感兴趣的研究人员而言,它应该是无价的。作为概念的证明,我们证明了RIP可以与单核苷酸多态性相似的方式用作生物标记。

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