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利用下一代转录组测序技术在大西洋鲱鱼(Clupea harengus)中发现 SNP。

SNP discovery using Next Generation Transcriptomic Sequencing in Atlantic herring (Clupea harengus).

机构信息

Molecular Ecology and Fisheries Genetics Laboratory, School of Biological Sciences, College of Natural Sciences, Bangor University, Bangor, Gwynedd, United Kingdom.

出版信息

PLoS One. 2012;7(8):e42089. doi: 10.1371/journal.pone.0042089. Epub 2012 Aug 7.

Abstract

The introduction of Next Generation Sequencing (NGS) has revolutionised population genetics, providing studies of non-model species with unprecedented genomic coverage, allowing evolutionary biologists to address questions previously far beyond the reach of available resources. Furthermore, the simple mutation model of Single Nucleotide Polymorphisms (SNPs) permits cost-effective high-throughput genotyping in thousands of individuals simultaneously. Genomic resources are scarce for the Atlantic herring (Clupea harengus), a small pelagic species that sustains high revenue fisheries. This paper details the development of 578 SNPs using a combined NGS and high-throughput genotyping approach. Eight individuals covering the species distribution in the eastern Atlantic were bar-coded and multiplexed into a single cDNA library and sequenced using the 454 GS FLX platform. SNP discovery was performed by de novo sequence clustering and contig assembly, followed by the mapping of reads against consensus contig sequences. Selection of candidate SNPs for genotyping was conducted using an in silico approach. SNP validation and genotyping were performed simultaneously using an Illumina 1,536 GoldenGate assay. Although the conversion rate of candidate SNPs in the genotyping assay cannot be predicted in advance, this approach has the potential to maximise cost and time efficiencies by avoiding expensive and time-consuming laboratory stages of SNP validation. Additionally, the in silico approach leads to lower ascertainment bias in the resulting SNP panel as marker selection is based only on the ability to design primers and the predicted presence of intron-exon boundaries. Consequently SNPs with a wider spectrum of minor allele frequencies (MAFs) will be genotyped in the final panel. The genomic resources presented here represent a valuable multi-purpose resource for developing informative marker panels for population discrimination, microarray development and for population genomic studies in the wild.

摘要

下一代测序(NGS)的引入彻底改变了群体遗传学,为非模式物种的研究提供了前所未有的基因组覆盖范围,使进化生物学家能够解决以前远远超出可用资源范围的问题。此外,单核苷酸多态性(SNP)的简单突变模型允许在数千个个体中同时进行具有成本效益的高通量基因分型。大西洋鲱(Clupea harengus)的基因组资源稀缺,它是一种小型洄游物种,支撑着高收入的渔业。本文详细介绍了使用组合 NGS 和高通量基因分型方法开发的 578 个 SNP。8 个个体涵盖了大西洋东部的物种分布范围,被条形码编码并混合到单个 cDNA 文库中,然后使用 454 GS FLX 平台进行测序。SNP 的发现是通过从头测序聚类和 contig 组装来完成的,然后是将读取映射到共识 contig 序列。候选 SNP 用于基因分型的选择是通过计算机模拟方法进行的。 SNP 的验证和基因分型同时使用 Illumina 1,536 GoldenGate 测定法进行。虽然基因分型测定中候选 SNP 的转换率不能预先预测,但这种方法有可能通过避免昂贵且耗时的 SNP 验证实验室阶段来最大限度地提高成本和时间效率。此外,由于基于仅能够设计引物和预测内含子-外显子边界的能力来选择标记,因此在最终的 SNP 面板中会检测到具有更广泛的次要等位基因频率(MAF)的 SNP。本文介绍的基因组资源是一个有价值的多用途资源,可用于开发用于群体识别、微阵列开发和野生种群基因组研究的信息标记面板。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6838/3413699/da914ebcbb9f/pone.0042089.g001.jpg

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