ezRAD: a simplified method for genomic genotyping in non-model organisms

被引:162
作者
Toonen, Robert J. [1 ]
Puritz, Jonathan B. [1 ]
Forsman, Zac H. [1 ]
Whitney, Jonathan L. [1 ]
Fernandez-Silva, Iria [1 ]
Andrews, Kimberly R. [1 ]
Bird, Christopher E. [2 ]
机构
[1] Univ Hawaii Manoa, Sch Ocean & Earth Sci & Technol, Hawaii Inst Marine Biol, Kaneohe, HI 96744 USA
[2] Texas A&M Univ, Dept Life Sci, Corpus Christi, TX USA
基金
美国国家科学基金会; 美国海洋和大气管理局;
关键词
RAD tag; RADseq; RAD-seq; Restriction site associated DNA (RAD); Next-generation sequencing; NGS; Genotype-by-sequencing; SNP DISCOVERY; RAD; PHYLOGEOGRAPHY; FORMAT;
D O I
10.7717/peerj.203
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Here, we introduce ezRAD, a novel strategy for restriction site-associated DNA (RAD) that requires little technical expertise or investment in laboratory equipment, and demonstrate its utility for ten non-model organisms across a wide taxonomic range. ezRAD differs from other RAD methods primarily through its use of standard Illumina TruSeq library preparation kits, which makes it possible for any laboratory to send out to a commercial genomic core facility for library preparation and next-generation sequencing with virtually no additional investment beyond the cost of the service itself. This simplification opens RADseq to any lab with the ability to extract DNA and perform a restriction digest. ezRAD also differs from others in its flexibility to use any restriction enzyme (or combination of enzymes) that cuts frequently enough to generate fragments of the desired size range, without requiring the purchase of separate adapters for each enzyme or a sonication step, which can further decrease the cost involved in choosing optimal enzymes for particular species and research questions. We apply this method across a wide taxonomic diversity of non-model organisms to demonstrate the utility and flexibility of our approach. The simplicity of ezRAD makes it particularly useful for the discovery of single nucleotide polymorphisms and targeted amplicon sequencing in natural populations of non-model organisms that have been historically understudied because of lack of genomic information.
引用
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页数:15
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