Department of Plant Sciences, University of Oxford, South Parks Road, Oxford OX1 3RB, UK.
BMC Genomics. 2013 Sep 24;14:653. doi: 10.1186/1471-2164-14-653.
The analysis of polyploid genomes is problematic because homeologous subgenome sequences are closely related. This relatedness makes it difficult to assign individual sequences to the specific subgenome from which they are derived, and hinders the development of polyploid whole genome assemblies.
We here present a next-generation sequencing (NGS)-based approach for assignment of subgenome-specific base-identity at sites containing homeolog-specific polymorphisms (HSPs): 'HSP base Assignment using NGS data through Diploid Similarity' (HANDS). We show that HANDS correctly predicts subgenome-specific base-identity at >90% of assayed HSPs in the hexaploid bread wheat (Triticum aestivum) transcriptome, thus providing a substantial increase in accuracy versus previous methods for homeolog-specific base assignment.
We conclude that HANDS enables rapid and accurate genome-wide discovery of homeolog-specific base-identity, a capability having multiple applications in polyploid genomics.
多倍体基因组的分析存在问题,因为同源亚基因组序列密切相关。这种相关性使得难以将单个序列分配到它们所源自的特定亚基因组,并且阻碍了多倍体全基因组组装的发展。
我们在这里提出了一种基于下一代测序(NGS)的方法,用于在含有同源特异性多态性(HSP)的位点上分配亚基因组特异性碱基身份:“通过二倍体相似性使用 NGS 数据进行 HSP 碱基分配”(HANDS)。我们表明,HANDS 正确预测了在六倍体普通小麦(Triticum aestivum)转录组中 >90%的测定 HSP 中的亚基因组特异性碱基身份,从而相对于以前用于同源特异性碱基分配的方法大大提高了准确性。
我们得出结论,HANDS 能够快速准确地发现全基因组同源特异性碱基身份,这在多倍体基因组学中有多种应用。