Ecology and Genetics Research Unit, University of Oulu, Oulu, Finland.
Zoology Unit, Finnish Museum of Natural History, University of Helsinki, Helsinki, Finland.
Methods Mol Biol. 2024;2744:213-221. doi: 10.1007/978-1-0716-3581-0_13.
Double-digest restriction site-associated DNA sequencing is a library preparation protocol that enables capturing variable sites across the genome including single-nucleotide polymorphisms (SNPs). These SNPs can be utilized to gain evolutionary insights into patterns observed in DNA barcodes, to infer population structure and phylogenies, to detect gene flow and introgression, and to perform species delimitation analyses. The protocol includes chemically shearing genomic DNA with restriction enzymes, unique tagging, size selection, and amplification of the resulting DNA fragments. Here we provide a detailed description of each step of the protocol, as well as information on essential equipment and common issues encountered during laboratory work.
双酶切限制位点相关 DNA 测序是一种文库制备方案,可捕获基因组中包括单核苷酸多态性(SNP)在内的可变位点。这些 SNP 可用于深入了解 DNA 条形码中观察到的模式的进化情况,推断种群结构和系统发育,检测基因流和渐渗,以及进行物种界限分析。该方案包括用限制性内切酶化学剪切基因组 DNA、独特标记、大小选择以及扩增所得 DNA 片段。在这里,我们详细描述了该方案的每一步,以及实验室工作中遇到的关键设备和常见问题的信息。