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内切酶 V 辅助下,通过脱氧肌苷和脱氧核苷硫代磷酸酯控制的寡核苷酸探针的精确切割,用于连接测序。

Endonuclease V-assisted accurate cleavage of oligonucleotide probes controlled by deoxyinosine and deoxynucleoside phosphorothioate for sequencing-by-ligation.

机构信息

State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, PR China.

出版信息

Analyst. 2012 Oct 7;137(19):4421-4. doi: 10.1039/c2an35595g.

Abstract

Sequencing-by-ligation (SBL) is one of the next-generation sequencing methods for massive parallel sequencing. The ligated probes used in SBL should be accurately cleaved for a better ligation in the next cycle. Here, a novel kind of oligonucleotide probe that could be accurately cleaved at the given position was proposed. Deoxynucleoside phosphorothioates were introduced into the deoxyoxanosine-containing oligonucleotide probes in order to increase the cleavage accuracy of endonuclease V on double-stranded DNA templates. The results illustrated that incorporating deoxynucleoside phosphorothioates could greatly reduce the effect of the nonsynchronous sequencing primer, and the queried bases of the DNA templates were unambiguously identified with 5 cycles of sequencing ligations. Additionally, the read length can reach up to 25 bp with high accuracy. The SBL-based method is inexpensive, has high-throughput, and is easy to operate allowing massive scale-up, miniaturization and automation.

摘要

连接测序(SBL)是一种大规模并行测序的下一代测序方法。SBL 中使用的连接探针应在下次循环中准确切割,以实现更好的连接。在此,提出了一种新型的寡核苷酸探针,它可以在给定位置准确切割。为了提高内切酶 V 在双链 DNA 模板上的切割准确性,在含脱氧氧杂环核苷的寡核苷酸探针中引入了脱氧核苷酸硫代磷酸酯。结果表明,引入脱氧核苷酸硫代磷酸酯可以大大降低非同步测序引物的影响,并且可以通过 5 轮测序连接明确识别 DNA 模板的查询碱基。此外,读长可以达到 25bp 且具有很高的准确性。基于 SBL 的方法成本低、高通量、易于操作,可以大规模扩展、小型化和自动化。

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