利用下一代测序进行全基因组遗传标记发现和基因分型。
Genome-wide genetic marker discovery and genotyping using next-generation sequencing.
机构信息
Institute of Evolutionary Biology, University of Edinburgh, Ashworth Laboratories, King's Buildings, West Mains Road, Edinburgh, EH9 3JT, UK.
出版信息
Nat Rev Genet. 2011 Jun 17;12(7):499-510. doi: 10.1038/nrg3012.
The advent of next-generation sequencing (NGS) has revolutionized genomic and transcriptomic approaches to biology. These new sequencing tools are also valuable for the discovery, validation and assessment of genetic markers in populations. Here we review and discuss best practices for several NGS methods for genome-wide genetic marker development and genotyping that use restriction enzyme digestion of target genomes to reduce the complexity of the target. These new methods -- which include reduced-representation sequencing using reduced-representation libraries (RRLs) or complexity reduction of polymorphic sequences (CRoPS), restriction-site-associated DNA sequencing (RAD-seq) and low coverage genotyping -- are applicable to both model organisms with high-quality reference genome sequences and, excitingly, to non-model species with no existing genomic data.
下一代测序(NGS)的出现彻底改变了生物学的基因组学和转录组学方法。这些新的测序工具对于遗传标记的发现、验证和评估也具有重要价值。在这里,我们回顾并讨论了几种用于全基因组遗传标记开发和基因分型的 NGS 方法的最佳实践,这些方法利用目标基因组的限制性内切酶消化来降低目标的复杂性。这些新方法——包括使用简化代表性文库(RRL)或多态序列复杂度降低(CRoPS)的简化代表性测序、限制性位点相关 DNA 测序(RAD-seq)和低覆盖率基因分型——既适用于具有高质量参考基因组序列的模式生物,也适用于没有现有基因组数据的令人兴奋的非模式物种。