Recent patents and challenges on DNA microarray probe design technologies.

Dan Tulpan
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引用次数: 5

Abstract

The invention of microarray technology has empowered scientists to quickly transition from single gene studies to massively parallel experiments investigating thousands of genes. The use of DNA microarrays relies on accurate design for probes that are immobilized on a surface and bind specifically to complementary targets in a complex solution. The quality of a set of DNA probes heavily relies on DNA hybridization - the process of joining two single-strands of DNA to form a double-stranded molecule, and is traditionally ensured by using specific design criteria. The design of DNA probes for microarrays requires very stringent criteria, due to the necessity of choosing unique sequences that perfectly complement specific regions from large genomic data sets, while avoiding hybridization with every other region of the same genome. Patents and research publications presenting various probe design methods are reviewed in this manuscript and future potential extensions of current technologies are suggested.

DNA微阵列探针设计技术的最新专利与挑战。
微阵列技术的发明使科学家能够迅速从单基因研究过渡到大规模并行实验,研究数千个基因。DNA微阵列的使用依赖于探针的精确设计,这些探针固定在表面上,并在复杂溶液中特异性地与互补目标结合。一组DNA探针的质量很大程度上依赖于DNA杂交——将两条单链DNA连接起来形成双链分子的过程,传统上是通过使用特定的设计标准来保证的。微阵列DNA探针的设计需要非常严格的标准,因为必须选择独特的序列,以完美地补充大型基因组数据集中的特定区域,同时避免与同一基因组的所有其他区域杂交。专利和研究出版物提出了各种探针设计方法,在这篇论文中进行了审查,并提出了当前技术的未来潜在扩展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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