Liao Rongrong, Wang Zhen, Chen Qiang, Tu Yingying, Chen Zhenliang, Wang Qishan, Yang Changsuo, Zhang Xiangzhe, Pan Yuchun
School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, China.
Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
PLoS One. 2015 Aug 27;10(8):e0137010. doi: 10.1371/journal.pone.0137010. eCollection 2015.
Single nucleotide polymorphisms (SNPs) are essential for identifying the genetic mechanisms of complex traits. In the present study, we applied genotyping by genome reducing and sequencing (GGRS) method to construct a 252-plex sequencing library for SNP discovery and genotyping in chicken. The library was successfully sequenced on an Illumina HiSeq 2500 sequencer with a paired-end pattern; approximately 400 million raw reads were generated, and an average of approximately 1.4 million good reads per sample were generated. A total of 91,767 SNPs were identified after strict filtering, and all of the 252 samples and all of the chromosomes were well represented. Compared with the Illumina 60K chicken SNP chip data, approximately 34,131 more SNPs were identified using GGRS, and a higher SNP density was found using GGRS, which could be beneficial for downstream analysis. Using the GGRS method, more than 3528 samples can be sequenced simultaneously, and the cost is reduced to $18 per sample. To the best of our knowledge, this study describes the first report of such highly multiplexed sequencing in chicken, indicating potential applications for genome-wide association and genomic selection in chicken.
单核苷酸多态性(SNPs)对于识别复杂性状的遗传机制至关重要。在本研究中,我们应用基因组缩减测序(GGRS)方法构建了一个252重测序文库,用于鸡的SNP发现和基因分型。该文库在Illumina HiSeq 2500测序仪上以双端模式成功测序;产生了约4亿条原始读数,每个样本平均产生约140万条优质读数。经过严格筛选后,共鉴定出91767个SNP,252个样本和所有染色体均得到了很好的覆盖。与Illumina 60K鸡SNP芯片数据相比,使用GGRS鉴定出的SNP多了约34131个,并且使用GGRS发现了更高的SNP密度,这可能有利于下游分析。使用GGRS方法,可以同时对超过3528个样本进行测序,成本降低至每个样本18美元。据我们所知,本研究描述了鸡中这种高度多重测序的首次报道,表明其在鸡的全基因组关联和基因组选择中的潜在应用。