Burford Reiskind M O, Coyle K, Daniels H V, Labadie P, Reiskind M H, Roberts N B, Roberts R B, Schaff J, Vargo E L
Department of Applied Ecology, North Carolina State University, Campus Box 7617, Raleigh, NC, 27695, USA.
Department of Biological Sciences, North Carolina State University, Raleigh, NC, 27695, USA.
Mol Ecol Resour. 2016 Nov;16(6):1303-1314. doi: 10.1111/1755-0998.12527. Epub 2016 May 17.
The generation of genome-scale data is critical for a wide range of questions in basic biology using model organisms, but also in questions of applied biology in nonmodel organisms (agriculture, natural resources, conservation and public health biology). Using a genome-scale approach on a diverse group of nonmodel organisms and with the goal of lowering costs of the method, we modified a multiplexed, high-throughput genomic scan technique utilizing two restriction enzymes. We analysed several pairs of restriction enzymes and completed double-digestion RAD sequencing libraries for nine different species and five genera of insects and fish. We found one particular enzyme pair produced consistently higher number of sequence-able fragments across all nine species. Building libraries off this enzyme pair, we found a range of usable SNPs between 4000 and 37 000 SNPS per species and we found a greater number of usable SNPs using reference genomes than de novo pipelines in STACKS. We also found fewer reads in the Read 2 fragments from the paired-end Illumina Hiseq run. Overall, the results of this study provide empirical evidence of the utility of this method for producing consistent data for diverse nonmodel species and suggest specific considerations for sequencing analysis strategies.
基因组规模数据的生成对于使用模式生物解决基础生物学中的广泛问题至关重要,对于非模式生物(农业、自然资源、保护生物学和公共卫生生物学)的应用生物学问题也同样重要。为了以基因组规模的方法研究不同种类的非模式生物,并降低该方法的成本,我们改进了一种利用两种限制性内切酶的多重高通量基因组扫描技术。我们分析了几对限制性内切酶,并为9个不同物种以及昆虫和鱼类的5个属完成了双酶切RAD测序文库的构建。我们发现,有一对特定的酶在所有9个物种中产生的可测序片段数量始终较高。基于这对酶构建文库,我们发现每个物种的可用单核苷酸多态性(SNP)数量在4000到37000之间,并且与STACKS中从头测序流程相比,使用参考基因组时能发现更多可用的SNP。我们还发现,在Illumina Hiseq双端测序运行的Read 2片段中读取的序列较少。总体而言,本研究结果为该方法用于为不同非模式物种生成一致数据的实用性提供了实证依据,并为测序分析策略提出了具体的考虑因素。