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Direct sequencing of haplotypes from diploid individuals through a modified emulsion PCR-based single-molecule sequencing approach

机译:通过改进的基于乳液PCR的单分子测序方法对二倍体个体的单倍型直接测序

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摘要

While standard DNA-sequencing approaches readily yield genotypic sequence data, haplotype information is often of greater utility for population genetic analyses. However, obtaining individual haplotype sequences can be costly and time-consuming and sometimes requires statistical reconstruction approaches that are subject to bias and error. Advancements have recently been made in determining individual chromosomal sequences in large-scale genomic studies, yet few options exist for obtaining this information from large numbers of highly polymorphic individuals in a cost-effective manner. As a solution, we developed a simple PCR-based method for obtaining sequence information from individual DNA strands using standard laboratory equipment. The method employs a water-in-oil emulsion to separate the PCR mixture into thousands of individual microreactors. PCR within these small vesicles results in amplification from only a single starting DNA template molecule and thus a single haplotype. We improved upon previous approaches by including SYBR Green I and a melted agarose solution in the PCR, allowing easy identification and separation of individually amplified DNA molecules. We demonstrate the use of this method on a highly polymorphic estuarine population of the copepod Eurytemora affinis for which current molecular and computational methods for haplotype determination have been inadequate.
机译:虽然标准的DNA测序方法很容易产生基因型序列数据,但单倍型信息通常在群体遗传分析中具有更大的实用性。然而,获得单个单倍型序列可能是昂贵且费时的,并且有时需要受到偏差和错误影响的统计重建方法。最近在大规模基因组研究中在确定单个染色体序列方面取得了进展,但是很少有选择以经济有效的方式从大量高度多态的个体获得此信息。作为解决方案,我们开发了一种简单的基于PCR的方法,可使用标准实验室设备从单个DNA链中获取序列信息。该方法采用油包水乳液将PCR混合物分离成数千个单个微反应器。这些小囊泡中的PCR仅从单个起始DNA模板分子开始扩增,从而从单个单倍型扩增。通过在PCR中加入SYBR Green I和融化的琼脂糖溶液,我们对以前的方法进行了改进,可轻松识别和分离单个扩增的DNA分子。我们证明了此方法对Eu足类Eurytemora affinis的高度多态河口种群的使用,对于这些种群而言,当前用于单倍型测定的分子和计算方法尚不充分。

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