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可扩展的组合式合成 DNA 组装用于跟踪应用。

Scalable Combinatorial Assembly of Synthetic DNA for Tracking Applications.

机构信息

Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.

Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO 80523, USA.

出版信息

Int J Mol Sci. 2023 Jan 29;24(3):2549. doi: 10.3390/ijms24032549.

Abstract

Synthetic DNA barcodes are double-stranded DNA molecules designed to carry recoverable information, information that can be used to represent and track objects and organisms. DNA barcodes offer robust, sensitive detection using standard amplification and sequencing techniques. While numerous research groups have promoted DNA as an information storage medium, less attention has been devoted to the design of economical, scalable DNA barcode libraries. Here, we present an alternative modular approach to sequence design. Barcode sequences were constructed from smaller, interchangeable blocks, allowing for the combinatorial assembly of numerous distinct tags. We demonstrated the design and construction of first-generation (N = 256) and second-generation (N = 512) modular barcode libraries, from fewer than 50 total single-stranded oligonucleotides for each library. To avoid contamination during experimental validation, a liquid-handling robot was employed for oligonucleotide mixing. Generating barcode sequences in-house reduces dependency upon external entities for unique tag generation, increasing flexibility in barcode generation and deployment. Next generation sequencing (NGS) detection of 256 different samples in parallel highlights the multiplexing afforded by the modular barcode design coupled with high-throughput sequencing. Deletion variant analysis of the first-generation library informed sequence design for enhancing barcode assembly specificity in the second-generation library.

摘要

合成 DNA 条码是双链 DNA 分子,旨在携带可恢复的信息,这些信息可用于表示和跟踪物体和生物。DNA 条码使用标准的扩增和测序技术提供强大、敏感的检测。虽然许多研究小组已经将 DNA 作为一种信息存储介质,但对经济、可扩展的 DNA 条码库的设计关注较少。在这里,我们提出了一种替代的序列设计模块化方法。条码序列由较小的、可互换的块构建而成,允许组合成许多不同的标签。我们展示了第一代(N = 256)和第二代(N = 512)模块化条码库的设计和构建,每个库使用的总单链寡核苷酸少于 50 个。为了避免在实验验证过程中的污染,我们使用液体处理机器人进行寡核苷酸混合。在内部生成条码序列可以减少对外部实体生成唯一标签的依赖,从而提高条码生成和部署的灵活性。下一代测序(NGS)能够同时平行检测 256 个不同的样本,突出了模块化条码设计与高通量测序相结合所提供的多路复用功能。第一代库的缺失变体分析为第二代库中增强条码组装特异性的序列设计提供了信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb07/9917336/03fd7585f6db/ijms-24-02549-g001.jpg

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