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核酸诊断技术的最新进展。

Recent advances in the development of nucleic acid diagnostics.

机构信息

National University of Ireland Galway, Ireland.

出版信息

Expert Rev Med Devices. 2010 Jul;7(4):529-39. doi: 10.1586/erd.10.22.

Abstract

Since the early 1970s, the use of nucleic acid sequences for specific diagnostic applications has followed a somewhat linear pattern of development. Early methods for restriction enzyme digestion, as well as reverse transcription, were followed in the late 1970s by Southern, northern and dot blotting, as well as DNA sequencing. In 1985, the description of PCR and the routine laboratory manipulation of sufficient quantities of DNA for diagnostics, resulted in the exponential growth of molecular biology. Subsequently, alternative DNA and RNA amplification protocols followed. The last 10 years have seen the second explosion in molecular biology with the development of real-time quantitative PCR and oligonucleotide microarrays. This advancement continues with the development of methods for 'direct' nucleic acid target detection from samples without in vitro amplification, and enhanced transduction elements for improved sensitivity of nucleic acid detection. In this article, we will describe the current state of the art in nucleic acid diagnostics, the use of nucleic acid-based diagnostics in clinical practice and the emerging technologies in the field. Finally, we will describe future trends and expected advances in the field.

摘要

自 20 世纪 70 年代初以来,核酸序列在特定诊断应用中的使用遵循了一种相对线性的发展模式。70 年代末,出现了限制酶消化以及反转录等早期方法,随后出现了 Southern、northern 和点印迹杂交以及 DNA 测序。1985 年,PCR 的描述以及常规实验室中用于诊断的足够数量的 DNA 的操作,使得分子生物学呈指数级增长。随后,出现了替代的 DNA 和 RNA 扩增方案。在过去的 10 年中,随着实时定量 PCR 和寡核苷酸微阵列的发展,分子生物学迎来了第二次爆炸。随着无需体外扩增即可从样本中直接检测核酸靶标方法的发展,以及用于提高核酸检测灵敏度的增强转导元件的发展,这一进展仍在继续。本文将描述核酸诊断的最新技术、核酸诊断在临床实践中的应用以及该领域新兴的技术。最后,我们将描述该领域未来的趋势和预期进展。

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