Custom-Primed Rolling Circle Amplicons for Highly Accurate Nanopore Sequencing

被引:0
|
作者
Zhang, Jiayi [1 ]
Yang, Xujuan [2 ]
Xuan, Weijia [1 ]
Wu, Zhiguang [1 ]
Ding, Jiawei [3 ]
Wang, Zhenqi [2 ]
Yan, Qi [1 ,4 ]
Zhang, Tianqing [1 ]
Qi, Zhi [3 ]
Bai, Jingwei [2 ]
Wei, Bryan [1 ]
机构
[1] Tsinghua Univ, Ctr Synthet & Syst Biol, Sch Life Sci, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Sch Pharmaceut Sci, Beijing 100084, Peoples R China
[3] Peking Univ, Acad Adv Interdisciplinary Studies, Ctr Quantitat Biol, Beijing 100084, Peoples R China
[4] Yale Univ, Cellular & Mol Physiol, New Haven, CT 06510 USA
来源
SMALL METHODS | 2025年
基金
国家重点研发计划;
关键词
consensus calling; nanopore sequencing; rolling circle amplification; PHI29; DNA-POLYMERASE; AMPLIFICATION; ENABLES; GENOME;
D O I
10.1002/smtd.202401416
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Tandem repeats of a certain DNA sequence can be generated using rolling circle amplification (RCA), where a circular template is continuously amplified by a polymerase with strand displacement activity. In leveraging the linear repetition of the target sequence, enhanced accuracy is achievable by consensus calling in nanopore sequencing. However, traditional multiply-primed RCA produces branched products with limited length, which may not be optimal for nanopore sequencing. In this study, an enhanced RCA protocol is introduced using sequence-specific primers to produce longer and less branched amplicons. Taking advantage of the RCA amplicons of tandem repeats, custom-primed rolling circle amplification sequencing (CPRSeq) is developed, a highly accurate nanopore sequencing pipeline. Utilizing CPRSeq, this successfully sequence standard samples of tumor-associated single nucleotide variants at low mutation frequency and accomplished the whole-genome sequencing and assembly of E. coli.
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页数:7
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