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少即是多:利用Ion Torrent半导体技术通过简化基因组测序(ddRAD)实现极端的基因组复杂性降低

Less is more: extreme genome complexity reduction with ddRAD using Ion Torrent semiconductor technology.

作者信息

Pukk Lilian, Ahmad Freed, Hasan Shihab, Kisand Veljo, Gross Riho, Vasemägi Anti

机构信息

Department of Aquaculture, Estonian University of Life Sciences, Tartu, 51006, Estonia.

Department of Information Technology, University of Turku, Turku, 20014, Finland.

出版信息

Mol Ecol Resour. 2015 Sep;15(5):1145-52. doi: 10.1111/1755-0998.12392. Epub 2015 Mar 10.

Abstract

Massively parallel sequencing a small proportion of the whole genome at high coverage enables answering a wide range of questions from molecular evolution and evolutionary biology to animal and plant breeding and forensics. In this study, we describe the development of restriction-site associated DNA (RAD) sequencing approach for Ion Torrent PGM platform. Our protocol results in extreme genome complexity reduction using two rare-cutting restriction enzymes and strict size selection of the library allowing sequencing of a relatively small number of genomic fragments with high sequencing depth. We applied this approach to a common freshwater fish species, the Eurasian perch (Perca fluviatilis L.), and generated over 2.2 MB of novel sequence data consisting of ~17,000 contigs, identified 1259 single nucleotide polymorphisms (SNPs). We also estimated genetic differentiation between the DNA pools from freshwater (Lake Peipus) and brackish water (the Baltic Sea) populations and identified SNPs with the strongest signal of differentiation that could be used for robust individual assignment in the future. This work represents an important step towards developing genomic resources and genetic tools for the Eurasian perch. We expect that our ddRAD sequencing protocol for semiconductor sequencing technology will be useful alternative for currently available RAD protocols.

摘要

在高覆盖率下对一小部分全基因组进行大规模平行测序,能够回答从分子进化、进化生物学到动植物育种及法医学等广泛问题。在本研究中,我们描述了用于Ion Torrent PGM平台的限制性内切酶相关DNA(RAD)测序方法的开发。我们的方案通过使用两种稀有切割限制性内切酶以及对文库进行严格的大小选择,极大地降低了基因组复杂性,从而能够对相对较少数量的基因组片段进行高深度测序。我们将此方法应用于一种常见的淡水鱼——欧亚鲈(Perca fluviatilis L.),生成了超过2.2 MB的新序列数据,包含约17,000个重叠群,鉴定出1259个单核苷酸多态性(SNP)。我们还估计了来自淡水(派普斯湖)和咸淡水(波罗的海)种群的DNA池之间的遗传分化,并鉴定出具有最强分化信号的SNP,这些SNP未来可用于可靠的个体分配。这项工作是朝着开发欧亚鲈的基因组资源和遗传工具迈出的重要一步。我们预计,我们用于半导体测序技术的ddRAD测序方案将成为当前可用RAD方案的有用替代方案。

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