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Novel Tools for Conservation Genomics: Comparing Two High-Throughput Approaches for SNP Discovery in the Transcriptome of the European Hake

机译:保护基因组学的新颖工具:比较欧洲无须鳕转录组中用于发现SNP的两种高通量方法

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摘要

The growing accessibility to genomic resources using next-generation sequencing (NGS) technologies has revolutionized the application of molecular genetic tools to ecology and evolutionary studies in non-model organisms. Here we present the case study of the European hake (Merluccius merluccius), one of the most important demersal resources of European fisheries. Two sequencing platforms, the Roche 454 FLX (454) and the Illumina Genome Analyzer (GAII), were used for Single Nucleotide Polymorphisms (SNPs) discovery in the hake muscle transcriptome. De novo transcriptome assembly into unique contigs, annotation, and in silico SNP detection were carried out in parallel for 454 and GAII sequence data. High-throughput genotyping using the Illumina GoldenGate assay was performed for validating 1,536 putative SNPs. Validation results were analysed to compare the performances of 454 and GAII methods and to evaluate the role of several variables (e.g. sequencing depth, intron-exon structure, sequence quality and annotation). Despite well-known differences in sequence length and throughput, the two approaches showed similar assay conversion rates (approximately 43%) and percentages of polymorphic loci (67.5% and 63.3% for GAII and 454, respectively). Both NGS platforms therefore demonstrated to be suitable for large scale identification of SNPs in transcribed regions of non-model species, although the lack of a reference genome profoundly affects the genotyping success rate. The overall efficiency, however, can be improved using strict quality and filtering criteria for SNP selection (sequence quality, intron-exon structure, target region score).
机译:使用下一代测序(NGS)技术获取基因组资源的机会日益增加,彻底改变了分子遗传工具在非模式生物中的生态学和进化研究中的应用。在这里,我们以欧洲无须鳕(Merluccius merluccius)为例,这是欧洲渔业最重要的沉没资源之一。使用两个测序平台Roche 454 FLX(454)和Illumina基因组分析仪(GAII)进行了无核肌肉转录组中单核苷酸多态性(SNP)的发现。从头转录组组装成独特的重叠群,注释和计算机SNP检测是针对454和GAII序列数据并行进行的。使用Illumina GoldenGate分析进行高通量基因分型,以验证1,536个假定的SNP。分析了验证结果以比较454和GAII方法的性能并评估几个变量的作用(例如测序深度,内含子-外显子结构,序列质量和注释)。尽管众所周知,序列长度和通量存在差异,但这两种方法仍显示出相似的测定转化率(约43%)和多态位点的百分比(GAII和454分别为67.5%和63.3%)。因此,两个NGS平台均被证明适用于非模型物种转录区中的SNP的大规模鉴定,尽管缺少参考基因组会深刻影响基因型成功率。但是,可以使用严格的质量和SNP选择的筛选标准(序列质量,内含子-外显子结构,目标区域得分)来提高总体效率。

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