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ezRAD:一种简化的非模式生物基因组基因分型方法。

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

机构信息

Hawai'i Institute of Marine Biology, School of Ocean & Earth Sciences & Technology, University of Hawai'i at Mānoa , Coconut Island, Kāne'ohe, HI , United States.

出版信息

PeerJ. 2013 Nov 19;1:e203. doi: 10.7717/peerj.203. eCollection 2013.

Abstract

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.

摘要

在这里,我们介绍了一种新的 RAD 方法 ezRAD,该方法对实验室设备和技术专业知识的要求较低,并且在跨广泛的分类群的十个非模式生物中证明了其有用性。ezRAD 与其他 RAD 方法的主要区别在于它使用了标准的 Illumina TruSeq 文库制备试剂盒,这使得任何实验室都可以将其送到商业基因组核心设施进行文库制备和下一代测序,而除了服务本身的成本之外,几乎不需要额外的投资。这种简化使得 RADseq 能够适用于任何能够提取 DNA 并进行限制酶切的实验室。ezRAD 还与其他方法的不同之处在于,它可以灵活地使用任何足以产生所需大小范围片段的限制酶(或组合),而无需为每种酶单独购买适配器或进行超声处理步骤,这可以进一步降低为特定物种和研究问题选择最佳酶的成本。我们将这种方法应用于广泛的非模式生物分类多样性中,以展示我们方法的实用性和灵活性。ezRAD 的简单性使其特别适用于发现非模式生物自然种群中的单核苷酸多态性和靶向扩增子测序,这些生物由于缺乏基因组信息而在历史上受到的研究较少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac09/3840413/6031b51c4a87/peerj-01-203-g001.jpg

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