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Allele Identification for Transcriptome-Based Population Genomics in the Invasive Plant Centaurea solstitialis

机译:入侵植物矢车菊基于转录组的种群基因组学的等位基因鉴定。

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摘要

Transcriptome sequences are becoming more broadly available for multiple individuals of the same species, providing opportunities to derive population genomic information from these datasets. Using the 454 Life Science Genome Sequencer FLX and FLX-Titanium next-generation platforms, we generated 11−430 Mbp of sequence for normalized cDNA for 40 wild genotypes of the invasive plant Centaurea solstitialis, yellow starthistle, from across its worldwide distribution. We examined the impact of sequencing effort on transcriptome recovery and overlap among individuals. To do this, we developed two novel publicly available software pipelines: SnoWhite for read cleaning before assembly, and AllelePipe for clustering of loci and allele identification in assembled datasets with or without a reference genome. AllelePipe is designed specifically for cases in which read depth information is not appropriate or available to assist with disentangling closely related paralogs from allelic variation, as in transcriptome or previously assembled libraries. We find that modest applications of sequencing effort recover most of the novel sequences present in the transcriptome of this species, including single-copy loci and a representative distribution of functional groups. In contrast, the coverage of variable sites, observation of heterozygosity, and overlap among different libraries are all highly dependent on sequencing effort. Nevertheless, the information gained from overlapping regions was informative regarding coarse population structure and variation across our small number of population samples, providing the first genetic evidence in support of hypothesized invasion scenarios.
机译:转录组序列对于相同物种的多个个体变得越来越广泛,为从这些数据集中推导种群基因组信息提供了机会。使用454生命科学基因组测序仪FLX和FLX-Titanium下一代平台,我们从全球分布的入侵植物Centaurea solstitialis的40种野生基因型中产生了11−430 Mbp的归一化cDNA序列。我们检查了测序工作对转录组恢复和个体之间重叠的影响。为此,我们开发了两个新颖的可公开获得的软件管道:SnoWhite用于在组装前进行读取清洗,以及AllelePipe用于在有或没有参考基因组的组装数据集中进行基因座的聚类和等位基因鉴定。 AllelePipe是专门为以下情况设计的:在转录组或先前组装的文库中,读取深度信息不适当或无法帮助将紧密相关的旁系同源物与等位基因变异区分开。我们发现,测序工作的适度应用可以恢复该物种转录组中存在的大多数新序列,包括单拷贝基因座和功能性基团的代表性分布。相反,可变位点的覆盖,杂合性的观察以及不同文库之间的重叠都高度依赖于测序工作。然而,从重叠区域获得的信息对于我们的少数种群样本中的粗略种群结构和变异提供了信息,为支持假设的入侵场景提供了第一个遗传证据。

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