Antipova Alena A, Sokolsky Tanya D, Clouser Christopher R, Dimalanta Eileen T, Hendrickson Cynthia L, Kosnopo Cisilya, Lee Clarence C, Ranade Swati S, Zhang Lei, Blanchard Alan P, McKernan Kevin J
ABI, Beverly, Massachusetts 01915, USA.
J Biomol Tech. 2009 Dec;20(5):253-7.
Identifying genetic variants and mutations that underlie human diseases requires development of robust, cost-effective tools for routine resequencing of regions of interest in the human genome. Here, we demonstrate that coupling Applied Biosystems SOLiD system-sequencing platform with microarray capture of targeted regions provides an efficient and robust method for high-coverage resequencing and polymorphism discovery in human protein-coding exons.
识别构成人类疾病基础的基因变异和突变,需要开发强大且经济高效的工具,用于对人类基因组中感兴趣区域进行常规重测序。在此,我们证明,将应用生物系统公司的SOLiD系统测序平台与靶向区域的微阵列捕获相结合,为人类蛋白质编码外显子的高覆盖度重测序和多态性发现提供了一种高效且强大的方法。