Capturing single‐copy nuclear genes, organellar genomes, and nuclear ribosomal DNA from deep genome skimming data for plant phylogenetics: A case study in Vitaceae

核基因 维他科 基因组 生物 核DNA 系统发育学 核糖体RNA 基因 核糖体DNA 遗传学 DNA 进化生物学 计算生物学 线粒体DNA 植物 葡萄
作者
Binbin Liu,Zhi‐Yao Ma,Chen Ren,Richard G. J. Hodel,Miao Sun,Xiu‐Qun Liu,Guang‐Ning Liu,Hong De‐Yuan,Elizabeth A. Zimmer,Jun Wen
出处
期刊:Journal of Systematics and Evolution [Wiley]
卷期号:59 (5): 1124-1138 被引量:87
标识
DOI:10.1111/jse.12806
摘要

With the decreasing cost and availability of many newly developed bioinformatics pipelines, next-generation sequencing (NGS) has revolutionized plant systematics in recent years. Genome skimming has been widely used to obtain high-copy fractions of the genomes, including plastomes, mitochondrial DNA (mtDNA), and nuclear ribosomal DNA (nrDNA). In this study, through simulations, we evaluated the optimal (minimum) sequencing depth and performance for recovering single-copy nuclear genes (SCNs) from genome skimming data, by subsampling genome resequencing data and generating 10 data sets with different sequencing coverage in silico. We tested the performance of four data sets (plastome, nrDNA, mtDNA, and SCNs) obtained from genome skimming based on phylogenetic analyses of the Vitis clade at the genus level and Vitaceae at the family level, respectively. Our results showed that optimal minimum sequencing depth for high-quality SCNs assembly via genome skimming was about 10× coverage. Without the steps of synthesizing baits and enrichment experiments, coupled with incredibly low sequencing costs, we showcase that deep genome skimming (DGS) is as effective for capturing large data sets of SCNs as the widely used Hyb-Seq approach, in addition to capturing plastomes, mtDNA, and entire nrDNA repeats. DGS may serve as an efficient and economical alternative and may be superior to the popular target enrichment/Hyb-Seq approach.
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