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SNP Discovery in the Transcriptome of White Pacific Shrimp Litopenaeus vannamei by Next Generation Sequencing

机译:下一代测序技术在南美白对虾南美白对虾转录组中的SNP发现

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摘要

The application of next generation sequencing technology has greatly facilitated high throughput single nucleotide polymorphism (SNP) discovery and genotyping in genetic research. In the present study, SNPs were discovered based on two transcriptomes of Litopenaeus vannamei (L. vannamei) generated from Illumina sequencing platform HiSeq 2000. One transcriptome of L. vannamei was obtained through sequencing on the RNA from larvae at mysis stage and its reference sequence was de novo assembled. The data from another transcriptome were downloaded from NCBI and the reads of the two transcriptomes were mapped separately to the assembled reference by BWA. SNP calling was performed using SAMtools. A total of 58,717 and 36,277 SNPs with high quality were predicted from the two transcriptomes, respectively. SNP calling was also performed using the reads of two transcriptomes together, and a total of 96,040 SNPs with high quality were predicted. Among these 96,040 SNPs, 5,242 and 29,129 were predicted as non-synonymous and synonymous SNPs respectively. Characterization analysis of the predicted SNPs in L. vannamei showed that the estimated SNP frequency was 0.21% (one SNP per 476 bp) and the estimated ratio for transition to transversion was 2.0. Fifty SNPs were randomly selected for validation by Sanger sequencing after PCR amplification and 76% of SNPs were confirmed, which indicated that the SNPs predicted in this study were reliable. These SNPs will be very useful for genetic study in L. vannamei, especially for the high density linkage map construction and genome-wide association studies.
机译:下一代测序技术的应用极大地促进了遗传研究中的高通量单核苷酸多态性(SNP)发现和基因分型。在本研究中,基于Illumina测序平台HiSeq 2000产生的南美白对虾(L. vannamei)的两个转录组发现了SNP。通过对mysis阶段幼虫的RNA及其参考序列进行测序,获得了南美白对虾的一个转录组。是从头开始组装的。从NCBI下载了另一个转录组的数据,两个转录组的读数分别由BWA映射到了组装的参考文献中。 SNP调用是使用SAMtools执行的。从这两个转录组分别预测到总共有高质量的58,717和36,277个SNP。还使用两个转录组的读数一起执行SNP调用,并且预测了总共96,040个高质量的SNP。在这96,040个SNP中,分别预测了5,242和29,129个非同义和同义SNP。对南美白对虾中预测的SNP的特征分析表明,估计的SNP频率为0.21%(每476 bp一个SNP),估计的向转化的比率为2.0。 PCR扩增后,随机选择了50个SNP进行Sanger测序验证,确认了76%的SNP,这表明本研究中预测的SNP是可靠的。这些SNPs将对南美白对虾的遗传研究非常有用,特别是对于高密度连锁图谱构建和全基因组关联研究。

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