Lu Na, Qiao Yi, Lu Zuhong, Tu Jing
State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China.
Comput Struct Biotechnol J. 2023 Feb 23;21:1688-1696. doi: 10.1016/j.csbj.2023.02.034. eCollection 2023.
Multiple displacement amplification (MDA) based on isothermal random priming and high fidelity phi29 DNA polymerase-mediated processive extension has revolutionized the field of whole genome amplification by enabling the amplification of minute amounts of DNA, such as from a single cell, generating vast amounts of DNA with high genome coverage. Despite its advantages, MDA has its own challenges, one of the grandest being the formation of chimeric sequences (chimeras), which presents in all MDA products and seriously disturbs the downstream analysis. In this review, we provide a comprehensive overview of current research on MDA chimeras. We first reviewed the mechanisms of chimera formation and chimera detection methods. We then systematically summarized the characteristics of chimeras, including overlap, chimeric distance, chimeric density, and chimeric rate, as found in independently published sequencing data. Finally, we reviewed the methods used to process chimeric sequences and their impacts on the improvement of data utilization efficiency. The information presented in this review will be useful for those interested in understanding the challenges with MDA and in improving its performance.
基于等温随机引物延伸和高保真phi29 DNA聚合酶介导的连续延伸的多重置换扩增(MDA),通过能够扩增微量DNA(如来自单个细胞的DNA),生成具有高基因组覆盖率的大量DNA,彻底改变了全基因组扩增领域。尽管MDA有其优势,但它也有自身的挑战,其中最主要的挑战之一是嵌合序列(嵌合体)的形成,这种情况存在于所有MDA产物中,并严重干扰下游分析。在这篇综述中,我们全面概述了当前关于MDA嵌合体的研究。我们首先回顾了嵌合体形成的机制和嵌合体检测方法。然后,我们系统地总结了嵌合体的特征,包括在独立发表的测序数据中发现的重叠、嵌合距离、嵌合密度和嵌合率。最后,我们回顾了处理嵌合序列的方法及其对提高数据利用效率的影响。本综述提供的信息将有助于那些有兴趣了解MDA挑战并改善其性能的人。