Data from: RADcap: sequence capture of dual-digest RADseq libraries with identifiable duplicates and reduced missing data

Molecular ecologists seek to genotype hundreds to thousands of loci from hundreds to thousands of individuals at minimal cost per sample. Current methods, such as restriction site associated DNA sequencing (RADseq) and sequence capture, are constrained by costs associated with inefficient use of sequencing data and sample preparation. Here, we introduce RADcap, an approach that combines the major benefits of RADseq (low cost with specific start positions) with those of sequence capture (repeatable sequencing of specific loci) to significantly increase efficiency and reduce costs relative to current approaches. RADcap uses a new version of dual-digest RADseq (3RAD) to identify candidate SNP loci for capture bait design, and subsequently uses custom sequence capture baits to consistently enrich candidate SNP loci across many individuals. We combined this approach with a new library preparation method for identifying and removing PCR duplicates from 3RAD libraries, which allows researchers to process RADseq data using traditional pipelines, and we tested the RADcap method by genotyping sets of 96 to 384 Wisteria plants. Our results demonstrate that our RADcap method: (1) methodologically reduces (to <5%) and allows computational removal of PCR duplicate reads from data; (2) achieves 80-90% reads-on-target in 11 of 12 enrichments; (3) returns consistent coverage (≥4x) across >90% of individuals at up to 99.8% of the targeted loci; (4) produces consistently high occupancy matrices of genotypes across hundreds of individuals; and (5) costs significantly less than current approaches.分子生态学家致力于以最低的单样本成本，对数百至数千个个体的数百至数千个基因座进行基因分型。当前的研究方法，如限制性酶切位点相关DNA测序（restriction site associated DNA sequencing，RADseq）与序列捕获技术，受限于测序数据利用效率低下以及样本制备相关的成本瓶颈。在此，我们提出RADcap技术，该方法整合了限制性酶切位点相关DNA测序（RADseq）的核心优势（低成本且具备特定起始位点）与序列捕获技术的优势（可对特定基因座进行可重复测序），相较于现有技术可显著提升实验效率并降低成本。RADcap首先采用双酶切RADseq的新版本（3RAD）来鉴定可用于捕获探针设计的候选单核苷酸多态性（single nucleotide polymorphism，SNP）基因座，随后通过定制化序列捕获探针实现对大量个体中候选SNP基因座的一致性富集。我们将该技术与一种全新的文库制备方法相结合，该方法可从3RAD文库中鉴定并去除聚合酶链式反应（polymerase chain reaction，PCR）重复序列，使研究人员能够使用传统流程处理RADseq数据；此外，我们通过对96至384株紫藤（Wisteria）植株进行基因分型来验证RADcap技术的性能。我们的研究结果表明，RADcap技术具备以下优势：(1) 在方法学上将数据中的PCR重复读段占比降至5%以下，并可通过计算手段移除这些重复读段；(2) 在12次富集实验中的11次实现了80%~90%的靶区读段占比；(3) 在高达99.8%的目标基因座上，可在超过90%的受试个体中实现≥4倍的测序覆盖度；(4) 可在数百个个体中生成一致性优异的基因型占有率矩阵；(5) 相较于当前主流方法，实验成本显著降低。